Human (GRCh38.p14)
Description

amyloid beta precursor protein binding family A member 3 [Source:HGNC Symbol;Acc:HGNC:580]

Gene Synonyms

MINT3, X11L2

Location
About this transcript

This transcript has 11 exons, is annotated with 31 domains and features, is associated with 6478 variant alleles and maps to 431 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000316757.4APBA3-2012176575aaENSP00000315136.2
 
Protein coding
CCDS12110O96018 NM_004886.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000590064.1APBA3-2054250No protein-
 
Retained intron
--TSL:1
ENST00000588984.5APBA3-2031779No protein-
 
Retained intron
--TSL:2
ENST00000590238.1APBA3-206830No protein-
 
Retained intron
--TSL:5
ENST00000589934.1APBA3-204725No protein-
 
Retained intron
--TSL:2
ENST00000592826.1APBA3-208577No protein-
 
Retained intron
--TSL:2
ENST00000591678.1APBA3-207575No protein-
 
Retained intron
--TSL:1
ENST00000586991.1APBA3-202541No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 11, Coding exons: 10, Transcript length: 2,176 bps, Translation length: 575 residues

MANE

This MANE Select transcript contains ENSP00000315136 and matches to NM_004886.4 and NP_004877.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: O96018

CCDS

This transcript is a member of the Human CCDS set: CCDS12110

Transcript Support Level (TSL)

TSL:1

Version

ENST00000316757.4

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.