Human (GRCh38.p14)
Description

odontogenic, ameloblast associated [Source:HGNC Symbol;Acc:HGNC:26043]

Gene Synonyms

APIN, FLJ20513

Location
About this transcript

This transcript has 11 exons, is annotated with 11 domains and features, is associated with 3761 variant alleles and maps to 357 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000683306.1ODAM-2061355279aaENSP00000507531.1
 
Protein coding
CCDS3536A1E959 NM_017855.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1
ENST00000396094.6ODAM-2011319279aaENSP00000379401.2
 
Protein coding
CCDS3536A1E959 -GENCODE basicAPPRIS P1TSL:5
ENST00000510709.6ODAM-203780253aaENSP00000423070.2
 
Protein coding
D6RA81 -TSL:5CDS 3' incomplete
ENST00000514097.5ODAM-205680216aaENSP00000426106.1
 
Protein coding
H0YA46 -TSL:5CDS 5' incomplete
ENST00000510847.1ODAM-20460530aaENSP00000422100.1
 
Nonsense mediated decay
H0Y8T7 -TSL:3CDS 5' incomplete
ENST00000506248.1ODAM-202554No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 11, Coding exons: 10, Transcript length: 1,319 bps, Translation length: 279 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: A1E959

CCDS

This transcript is a member of the Human CCDS set: CCDS3536

Transcript Support Level (TSL)

TSL:5

Version

ENST00000396094.6

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.