Canonical Allele Identifier: CA2618973435

Gene: KRT8

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52897406T>C , CM000674.2:g.52897406T>C	GRCh38
NC_000012.11:g.53291190T>C , CM000674.1:g.53291190T>C	GRCh37
NC_000012.10:g.51577457T>C	NCBI36
NG_008402.1:g.12679A>G
NG_008402.2:g.57461A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692008.1:c.*22A>G MANE Select	ENSP00000509398.1:n.*22A>G
ENST00000293308.11:c.*22A>G	ENSP00000293308.6:n.*22A>G
ENST00000546583.5:n.2664A>G
ENST00000546897.5:c.*22A>G	ENSP00000447402.1:n.*22A>G
ENST00000550170.5:n.2012A>G
ENST00000552150.5:c.*22A>G	ENSP00000449404.1:n.*22A>G
ENST00000552551.5:c.*22A>G	ENSP00000447566.1:n.*22A>G
NM_001256282.1:c.*22A>G	NP_001243211.1:n.*22A>G
NM_001256293.1:c.*22A>G	NP_001243222.1:n.*22A>G
NM_002273.3:c.*22A>G	NP_002264.1:n.*22A>G
NR_045962.1:n.1931A>G
NM_001256282.2:c.*22A>G	NP_001243211.1:n.*22A>G
NM_001256293.2:c.*22A>G	NP_001243222.1:n.*22A>G
NM_002273.4:c.*22A>G MANE Select	NP_002264.1:n.*22A>G
NR_045962.2:n.1925A>G