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Human (GRCh37.p13)
Description

Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 [Source:HGNC Symbol;Acc:467]

Gene Synonyms

AMMERC1

About this transcript

This transcript has 3 exons, is associated with 25510 variant alleles and maps to 104 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000262844.5AMMECR1-0015504333aaENSP00000262844.5
 
Protein coding
CCDS14551Q9Y4X0 NM_015365.2Ensembl CanonicalGENCODE basic
ENST00000372057.1AMMECR1-0023380210aaENSP00000361127.1
 
Protein coding
CCDS55476Q9Y4X0 NM_001171689.1GENCODE basic
ENST00000372059.2AMMECR1-0053052296aaENSP00000361129.2
 
Protein coding
CCDS35368Q9Y4X0 NM_001025580.1GENCODE basic
ENST00000496695.1AMMECR1-004546No protein-
 
Processed transcript
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ENST00000473662.1AMMECR1-003418No protein-
 
Processed transcript
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Statistics

Exons: 3, Coding exons: 0, Transcript length: 418 bps,

Version

ENST00000473662.1

Type

Processed transcript

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
OTTHUMT00000057909 (version 1)