Canonical Allele Identifier: CA480077812

Gene: KRT8

Linked Data

• MyVariant Identifiers: chr12:g.53298508G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52904724G>C , CM000674.2:g.52904724G>C	GRCh38
NC_000012.11:g.53298508G>C , CM000674.1:g.53298508G>C	GRCh37
NC_000012.10:g.51584775G>C	NCBI36
NG_008402.1:g.5361C>G
NG_008402.2:g.50143C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692008.1:c.258C>G MANE Select	ENSP00000509398.1:p.Ala86=
ENST00000293308.11:c.258C>G	ENSP00000293308.6:p.Ala86=
ENST00000546542.1:c.492C>G	ENSP00000450228.1:p.Ala164=
ENST00000546583.5:n.329C>G
ENST00000546826.5:c.258C>G	ENSP00000447881.1:p.Ala86=
ENST00000546897.5:c.258C>G	ENSP00000447402.1:p.Ala86=
ENST00000548998.5:c.378C>G	ENSP00000447040.1:p.Ala126=
ENST00000550170.5:n.321C>G
ENST00000552150.5:c.342C>G	ENSP00000449404.1:p.Ala114=
ENST00000552551.5:c.258C>G	ENSP00000447566.1:p.Ala86=
NM_001256282.1:c.342C>G	NP_001243211.1:p.Ala114=
NM_001256293.1:c.258C>G	NP_001243222.1:p.Ala86=
NM_002273.3:c.258C>G	NP_002264.1:p.Ala86=
NR_045962.1:n.715C>G
NM_001256282.2:c.342C>G	NP_001243211.1:p.Ala114=
NM_001256293.2:c.258C>G	NP_001243222.1:p.Ala86=
NM_002273.4:c.258C>G MANE Select	NP_002264.1:p.Ala86=
NR_045962.2:n.709C>G