Human (GRCh38.p14)
Description

NCK associated protein 1 like [Source:HGNC Symbol;Acc:HGNC:4862]

Gene Synonyms

HEM1

Location
About this transcript

This transcript has 31 exons, is annotated with 5 domains and features, is associated with 19032 variant alleles and maps to 735 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000293373.11NCKAP1L-20189801127aaENSP00000293373.6
 
Protein coding
CCDS31813P55160-1 NM_005337.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000545638.2NCKAP1L-20236121077aaENSP00000445596.2
 
Protein coding
CCDS53799P55160-2 -GENCODE basicTSL:2
ENST00000548221.5NCKAP1L-2043559449aaENSP00000447246.1
 
Nonsense mediated decay
F8W050 -TSL:2
ENST00000552211.5NCKAP1L-208597No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000548916.1NCKAP1L-205708No protein-
 
Retained intron
--TSL:3
ENST00000547500.1NCKAP1L-203636No protein-
 
Retained intron
--TSL:2
ENST00000549451.1NCKAP1L-207629No protein-
 
Retained intron
--TSL:4
ENST00000548980.1NCKAP1L-206562No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 31, Coding exons: 30, Transcript length: 3,612 bps, Translation length: 1,077 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: P55160

CCDS

This transcript is a member of the Human CCDS set: CCDS53799

Transcript Support Level (TSL)

TSL:2

Version

ENST00000545638.2

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.