Description
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 [Source:HGNC Symbol;Acc:467]
Location
Chromosome X: 109,439,638-109,683,461 reverse strand.
Gene
This transcript is a product of gene ENSG00000101935 - This gene has 5 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
AMMECR1-001ENST000002628445504ENSP00000262844333Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS14551
AMMECR1-002ENST000003720573380ENSP00000361127210Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS55476
AMMECR1-005ENST000003720593052ENSP00000361129296Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS35368
AMMECR1-003ENST00000473662418No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
AMMECR1-004ENST00000496695546No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -

Transcript and Gene level displays

Views in Archive EnsEMBL are separated into gene based views and transcript based views according to which level the information is more appropriately associated with. This view is a transcript level view. To flip between the two sets of views you can click on the Gene and Transcript tabs in the menu bar at the top of the page.

Statistics

Exons: 8 Transcript length: 3,380 bps Translation length: 210 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS55476

Ensembl version

ENST00000372057.1

Type

Known protein coding

Prediction Method
Transcript where the Ensembl genebuild transcript and the Vega manual annotation have the same sequence, for every base pair. See article.
Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000057908 (version 2)