Canonical Allele Identifier: CA480077933

Gene: KRT8

Linked Data

• MyVariant Identifiers: chr12:g.53298547C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52904763C>A , CM000674.2:g.52904763C>A	GRCh38
NC_000012.11:g.53298547C>A , CM000674.1:g.53298547C>A	GRCh37
NC_000012.10:g.51584814C>A	NCBI36
NG_008402.1:g.5322G>T
NG_008402.2:g.50104G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692008.1:c.219G>T MANE Select	ENSP00000509398.1:p.Leu73=
ENST00000293308.11:c.219G>T	ENSP00000293308.6:p.Leu73=
ENST00000546542.1:c.453G>T	ENSP00000450228.1:p.Leu151=
ENST00000546583.5:n.290G>T
ENST00000546826.5:c.219G>T	ENSP00000447881.1:p.Leu73=
ENST00000546897.5:c.219G>T	ENSP00000447402.1:p.Leu73=
ENST00000548998.5:c.339G>T	ENSP00000447040.1:p.Leu113=
ENST00000550170.5:n.282G>T
ENST00000552150.5:c.303G>T	ENSP00000449404.1:p.Leu101=
ENST00000552551.5:c.219G>T	ENSP00000447566.1:p.Leu73=
NM_001256282.1:c.303G>T	NP_001243211.1:p.Leu101=
NM_001256293.1:c.219G>T	NP_001243222.1:p.Leu73=
NM_002273.3:c.219G>T	NP_002264.1:p.Leu73=
NR_045962.1:n.676G>T
NM_001256282.2:c.303G>T	NP_001243211.1:p.Leu101=
NM_001256293.2:c.219G>T	NP_001243222.1:p.Leu73=
NM_002273.4:c.219G>T MANE Select	NP_002264.1:p.Leu73=
NR_045962.2:n.670G>T