Description
Fanconi anemia, complementation group L [Source:HGNC Symbol;Acc:20748]
Location
Chromosome 2: 58,386,378-58,468,507 reverse strand.
Transcripts
This gene has 11 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
FANCL-001ENST000002337411683ENSP00000233741375Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS1860
FANCL-002ENST000004021351698ENSP00000385021380Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS46294
FANCL-003ENST00000449070964ENSP00000401280301Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
FANCL-004ENST000004032951576ENSP00000386097347Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
FANCL-005ENST00000417361545ENSP00000389448145Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
FANCL-006ENST00000403676849ENSP00000384046258Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
FANCL-007ENST00000446381487ENSP00000390991158Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
FANCL-009ENST00000427708864ENSP00000400969288Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
FANCL-201ENST00000540646906ENSP00000441431127Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
FANCL-008ENST00000481670368No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
FANCL-010ENST00000470506733No protein product-Retained intronNoncoding transcript containing intronic sequence. -

Transcript and Gene level displays

In Archive EnsEMBL we provide displays at two levels:

  • Transcript views which provide information specific to an individual transcript such as the cDNA and CDS sequences and protein domain annotation.
  • Gene views which provide displays for data associated at the gene level such as orthologues, paralogues, regulatory regions and splice variants.

This view is a gene level view. To access the transcript level displays select a Transcript ID in the table above and then navigate to the information you want using the menu at the left hand side of the page. To return to viewing gene level information click on the Gene tab in the menu bar at the top of the page.