Canonical Allele Identifier: CA2036710345

Gene: KRT8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52904822A= , CM000674.2:g.52904822A=	GRCh38
NC_000012.11:g.53298606A= , CM000674.1:g.53298606A=	GRCh37
NC_000012.10:g.51584873A=	NCBI36
NG_008402.1:g.5263T=
NG_008402.2:g.50045T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692008.1:c.160T= MANE Select	ENSP00000509398.1:p.Tyr54=
ENST00000293308.11:c.160T=	ENSP00000293308.6:p.Tyr54=
ENST00000546542.1:c.394T=	ENSP00000450228.1:p.Tyr132=
ENST00000546583.5:n.231T=
ENST00000546826.5:c.160T=	ENSP00000447881.1:p.Tyr54=
ENST00000546897.5:c.160T=	ENSP00000447402.1:p.Tyr54=
ENST00000548998.5:c.280T=	ENSP00000447040.1:p.Tyr94=
ENST00000550170.5:n.223T=
ENST00000552150.5:c.244T=	ENSP00000449404.1:p.Tyr82=
ENST00000552551.5:c.160T=	ENSP00000447566.1:p.Tyr54=
NM_001256282.1:c.244T=	NP_001243211.1:p.Tyr82=
NM_001256293.1:c.160T=	NP_001243222.1:p.Tyr54=
NM_002273.3:c.160T=	NP_002264.1:p.Tyr54=
NR_045962.1:n.617T=
NM_001256282.2:c.244T=	NP_001243211.1:p.Tyr82=
NM_001256293.2:c.160T=	NP_001243222.1:p.Tyr54=
NM_002273.4:c.160T= MANE Select	NP_002264.1:p.Tyr54=
NR_045962.2:n.611T=