Canonical Allele Identifier: CA500187239

Gene: KRT12

Linked Data

• MyVariant Identifiers: chr17:g.39023174G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40866922G>A , CM000679.2:g.40866922G>A	GRCh38
NC_000017.10:g.39023174G>A , CM000679.1:g.39023174G>A	GRCh37
NC_000017.9:g.36276700G>A	NCBI36
NG_008077.1:g.5289C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251643.5:c.265C>T MANE Select	ENSP00000251643.4:p.Leu89=
ENST00000647902.1:c.212-55C>T	ENSP00000497770.1:n.212-55C>T
ENST00000251643.4:c.265C>T	ENSP00000251643.4:p.Leu89=
NM_000223.3:c.265C>T	NP_000214.1:p.Leu89=
XR_934754.1:n.1500+16062G>A
XR_934754.2:n.2008+16062G>A
NM_000223.4:c.265C>T MANE Select	NP_000214.1:p.Leu89=