Canonical Allele Identifier: CA384997115

Gene: KRT8

Linked Data

• MyVariant Identifiers: chr12:g.53298543G>A (hg19) ; chr12:g.52904759G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52904759G>A , CM000674.2:g.52904759G>A	GRCh38
NC_000012.11:g.53298543G>A , CM000674.1:g.53298543G>A	GRCh37
NC_000012.10:g.51584810G>A	NCBI36
NG_008402.1:g.5326C>T
NG_008402.2:g.50108C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692008.1:c.223C>T MANE Select	ENSP00000509398.1:p.Pro75Ser
ENST00000293308.11:c.223C>T	ENSP00000293308.6:p.Pro75Ser
ENST00000546542.1:c.457C>T	ENSP00000450228.1:p.Pro153Ser
ENST00000546583.5:n.294C>T
ENST00000546826.5:c.223C>T	ENSP00000447881.1:p.Pro75Ser
ENST00000546897.5:c.223C>T	ENSP00000447402.1:p.Pro75Ser
ENST00000548998.5:c.343C>T	ENSP00000447040.1:p.Pro115Ser
ENST00000550170.5:n.286C>T
ENST00000552150.5:c.307C>T	ENSP00000449404.1:p.Pro103Ser
ENST00000552551.5:c.223C>T	ENSP00000447566.1:p.Pro75Ser
NM_001256282.1:c.307C>T	NP_001243211.1:p.Pro103Ser
NM_001256293.1:c.223C>T	NP_001243222.1:p.Pro75Ser
NM_002273.3:c.223C>T	NP_002264.1:p.Pro75Ser
NR_045962.1:n.680C>T
NM_001256282.2:c.307C>T	NP_001243211.1:p.Pro103Ser
NM_001256293.2:c.223C>T	NP_001243222.1:p.Pro75Ser
NM_002273.4:c.223C>T MANE Select	NP_002264.1:p.Pro75Ser
NR_045962.2:n.674C>T