Canonical Allele Identifier: CA2036710291

Gene: KRT8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52904788G= , CM000674.2:g.52904788G=	GRCh38
NC_000012.11:g.53298572G= , CM000674.1:g.53298572G=	GRCh37
NC_000012.10:g.51584839G=	NCBI36
NG_008402.1:g.5297C=
NG_008402.2:g.50079C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692008.1:c.194C= MANE Select	ENSP00000509398.1:p.Ala65=
ENST00000293308.11:c.194C=	ENSP00000293308.6:p.Ala65=
ENST00000546542.1:c.428C=	ENSP00000450228.1:p.Ala143=
ENST00000546583.5:n.265C=
ENST00000546826.5:c.194C=	ENSP00000447881.1:p.Ala65=
ENST00000546897.5:c.194C=	ENSP00000447402.1:p.Ala65=
ENST00000548998.5:c.314C=	ENSP00000447040.1:p.Ala105=
ENST00000550170.5:n.257C=
ENST00000552150.5:c.278C=	ENSP00000449404.1:p.Ala93=
ENST00000552551.5:c.194C=	ENSP00000447566.1:p.Ala65=
NM_001256282.1:c.278C=	NP_001243211.1:p.Ala93=
NM_001256293.1:c.194C=	NP_001243222.1:p.Ala65=
NM_002273.3:c.194C=	NP_002264.1:p.Ala65=
NR_045962.1:n.651C=
NM_001256282.2:c.278C=	NP_001243211.1:p.Ala93=
NM_001256293.2:c.194C=	NP_001243222.1:p.Ala65=
NM_002273.4:c.194C= MANE Select	NP_002264.1:p.Ala65=
NR_045962.2:n.645C=