Canonical Allele Identifier: CA144203

Gene: KRT8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52897468C>T , CM000674.2:g.52897468C>T	GRCh38
NC_000012.11:g.53291252C>T , CM000674.1:g.53291252C>T	GRCh37
NC_000012.10:g.51577519C>T	NCBI36
NG_008402.1:g.12617G>A
NG_008402.2:g.57399G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002273.4:c.1412G>A MANE Select	NP_002264.1:p.Gly471Glu
ENST00000692008.1:c.1412G>A MANE Select	ENSP00000509398.1:p.Gly471Glu
NM_001256282.1:c.1496G>A	NP_001243211.1:p.Gly499Glu
NM_001256282.2:c.1496G>A	NP_001243211.1:p.Gly499Glu
NM_001256293.1:c.1412G>A	NP_001243222.1:p.Gly471Glu
NM_001256293.2:c.1412G>A	NP_001243222.1:p.Gly471Glu
NM_002273.3:c.1412G>A	NP_002264.1:p.Gly471Glu
NR_045962.1:n.1869G>A
NR_045962.2:n.1863G>A
ENST00000293308.11:c.1412G>A	ENSP00000293308.6:p.Gly471Glu
ENST00000546583.5:n.2602G>A
ENST00000546897.5:c.1412G>A	ENSP00000447402.1:p.Gly471Glu
ENST00000550170.5:n.1950G>A
ENST00000552150.5:c.1496G>A	ENSP00000449404.1:p.Gly499Glu
ENST00000552551.5:c.1412G>A	ENSP00000447566.1:p.Gly471Glu