Canonical Allele Identifier: CA480078002

Gene: KRT8

Linked Data

• MyVariant Identifiers: chr12:g.53298580G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52904796G>C , CM000674.2:g.52904796G>C	GRCh38
NC_000012.11:g.53298580G>C , CM000674.1:g.53298580G>C	GRCh37
NC_000012.10:g.51584847G>C	NCBI36
NG_008402.1:g.5289C>G
NG_008402.2:g.50071C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692008.1:c.186C>G MANE Select	ENSP00000509398.1:p.Gly62=
ENST00000293308.11:c.186C>G	ENSP00000293308.6:p.Gly62=
ENST00000546542.1:c.420C>G	ENSP00000450228.1:p.Gly140=
ENST00000546583.5:n.257C>G
ENST00000546826.5:c.186C>G	ENSP00000447881.1:p.Gly62=
ENST00000546897.5:c.186C>G	ENSP00000447402.1:p.Gly62=
ENST00000548998.5:c.306C>G	ENSP00000447040.1:p.Gly102=
ENST00000550170.5:n.249C>G
ENST00000552150.5:c.270C>G	ENSP00000449404.1:p.Gly90=
ENST00000552551.5:c.186C>G	ENSP00000447566.1:p.Gly62=
NM_001256282.1:c.270C>G	NP_001243211.1:p.Gly90=
NM_001256293.1:c.186C>G	NP_001243222.1:p.Gly62=
NM_002273.3:c.186C>G	NP_002264.1:p.Gly62=
NR_045962.1:n.643C>G
NM_001256282.2:c.270C>G	NP_001243211.1:p.Gly90=
NM_001256293.2:c.186C>G	NP_001243222.1:p.Gly62=
NM_002273.4:c.186C>G MANE Select	NP_002264.1:p.Gly62=
NR_045962.2:n.637C>G