Human (GRCh38.p14)
Description

kelch domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19836]

Gene Synonyms

MST025

Location
About this transcript

This transcript has 13 exons, is annotated with 11 domains and features, is associated with 28372 variant alleles and maps to 428 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000359332.7KLHDC1-2012674406aaENSP00000352282.2
 
Protein coding
CCDS9692Q8N7A1 NM_172193.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000557128.1KLHDC1-206655196aaENSP00000451407.1
 
Protein coding
G3V3T1 -TSL:3CDS 3' incomplete
ENST00000553274.1KLHDC1-202645190aaENSP00000452543.2
 
Protein coding
G3V5V5 -TSL:3CDS 3' incomplete
ENST00000555704.5KLHDC1-204144767aaENSP00000451819.1
 
Nonsense mediated decay
G3V4I4 -TSL:1
ENST00000556392.5KLHDC1-205136096aaENSP00000450595.1
 
Nonsense mediated decay
G3V2D3 -TSL:1
ENST00000554512.1KLHDC1-203726No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 13, Coding exons: 13, Transcript length: 2,674 bps, Translation length: 406 residues

MANE

This MANE Select transcript contains ENSP00000352282 and matches to NM_172193.3 and NP_751943.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8N7A1

CCDS

This transcript is a member of the Human CCDS set: CCDS9692

Transcript Support Level (TSL)

TSL:1

Version

ENST00000359332.7

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.