Canonical Allele Identifier: CA2036663562

Gene: KRT4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814036A= , CM000674.2:g.52814036A=	GRCh38
NC_000012.11:g.53207820A= , CM000674.1:g.53207820A=	GRCh37
NC_000012.10:g.51494087A=	NCBI36
NG_007380.1:g.5516T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000551956.2:c.23T= MANE Select	ENSP00000448220.1:p.Val8=
ENST00000548097.5:c.23T=	ENSP00000449755.1:p.Val8=
ENST00000551956.1:c.23T=	ENSP00000448220.1:p.Val8=
ENST00000552668.1:c.23T=	ENSP00000447320.1:p.Val8=
NM_002272.3:c.23T=	NP_002263.3:p.Val8=
NM_002272.4:c.23T= MANE Select	NP_002263.3:p.Val8=