Canonical Allele Identifier: CA2036689014

Gene: KRT4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52807694C= , CM000674.2:g.52807694C=	GRCh38
NC_000012.11:g.53201478C= , CM000674.1:g.53201478C=	GRCh37
NC_000012.10:g.51487745C=	NCBI36
NG_007380.1:g.11858G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.2:c.1296G= MANE Select	ENSP00000448220.1:p.Leu432=
ENST00000548097.5:c.*808G=	ENSP00000449755.1:n.*808G=
ENST00000551956.1:c.1296G=	ENSP00000448220.1:p.Leu432=
NM_002272.3:c.1296G=	NP_002263.3:p.Leu432=
NM_002272.4:c.1296G= MANE Select	NP_002263.3:p.Leu432=