Canonical Allele Identifier: CA2036710301

Gene: KRT8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52904798C= , CM000674.2:g.52904798C=	GRCh38
NC_000012.11:g.53298582C= , CM000674.1:g.53298582C=	GRCh37
NC_000012.10:g.51584849C=	NCBI36
NG_008402.1:g.5287G=
NG_008402.2:g.50069G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002273.4:c.184G= MANE Select	NP_002264.1:p.Gly62=
ENST00000692008.1:c.184G= MANE Select	ENSP00000509398.1:p.Gly62=
NM_001256282.1:c.268G=	NP_001243211.1:p.Gly90=
NM_001256282.2:c.268G=	NP_001243211.1:p.Gly90=
NM_001256293.1:c.184G=	NP_001243222.1:p.Gly62=
NM_001256293.2:c.184G=	NP_001243222.1:p.Gly62=
NM_002273.3:c.184G=	NP_002264.1:p.Gly62=
NR_045962.1:n.641G=
NR_045962.2:n.635G=
ENST00000293308.11:c.184G=	ENSP00000293308.6:p.Gly62=
ENST00000546542.1:c.418G=	ENSP00000450228.1:p.Gly140=
ENST00000546583.5:n.255G=
ENST00000546826.5:c.184G=	ENSP00000447881.1:p.Gly62=
ENST00000546897.5:c.184G=	ENSP00000447402.1:p.Gly62=
ENST00000548998.5:c.304G=	ENSP00000447040.1:p.Gly102=
ENST00000550170.5:n.247G=
ENST00000552150.5:c.268G=	ENSP00000449404.1:p.Gly90=
ENST00000552551.5:c.184G=	ENSP00000447566.1:p.Gly62=