Human (GRCh38.p14)
Description

kinesin family member 12 [Source:HGNC Symbol;Acc:HGNC:21495]

Location

Chromosome 9: 114,086,126-114,099,292 reverse strand.

GRCh38:CM000671.2

About this gene

This gene has 8 transcripts (splice variants), 117 orthologues, 41 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000640217.2KIF12-2052195651aaENSP00000491702.1
 
Protein coding
CCDS94465A0A1W2PPS5 NM_001388308.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000643988.1KIF12-207502104aaENSP00000495410.1
 
Protein coding
A0A2R8Y6R2 -CDS 5' incomplete
ENST00000498016.1KIF12-203400122aaENSP00000491090.1
 
Protein coding
A0A1W2PNV5 -TSL:5CDS 5' incomplete
ENST00000473174.1KIF12-20173548aaENSP00000491357.1
 
Nonsense mediated decay
A0A1W2PP63 -TSL:5CDS 5' incomplete
ENST00000691154.1KIF12-20835257aaENSP00000510798.1
 
Nonsense mediated decay
A0A8I5KWX3 -CDS 5' incomplete
ENST00000639832.1KIF12-2042564No protein-
 
Retained intron
--TSL:2
ENST00000640553.1KIF12-2062003No protein-
 
Retained intron
--TSL:1
ENST00000491059.1KIF12-202367No protein-
 
Retained intron
--TSL:3