Canonical Allele Identifier: CA500187296

Gene: KRT12

Linked Data

• MyVariant Identifiers: chr17:g.39023202T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40866950T>A , CM000679.2:g.40866950T>A	GRCh38
NC_000017.10:g.39023202T>A , CM000679.1:g.39023202T>A	GRCh37
NC_000017.9:g.36276728T>A	NCBI36
NG_008077.1:g.5261A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251643.5:c.237A>T MANE Select	ENSP00000251643.4:p.Gly79=
ENST00000647902.1:c.211+26A>T	ENSP00000497770.1:n.211+26A>T
ENST00000251643.4:c.237A>T	ENSP00000251643.4:p.Gly79=
NM_000223.3:c.237A>T	NP_000214.1:p.Gly79=
XR_934754.1:n.1500+16090T>A
XR_934754.2:n.2008+16090T>A
NM_000223.4:c.237A>T MANE Select	NP_000214.1:p.Gly79=