Canonical Allele Identifier: CA399388912

Gene: KRT12

Linked Data

• MyVariant Identifiers: chr17:g.39023182C>T (hg19) ; chr17:g.40866930C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40866930C>T , CM000679.2:g.40866930C>T	GRCh38
NC_000017.10:g.39023182C>T , CM000679.1:g.39023182C>T	GRCh37
NC_000017.9:g.36276708C>T	NCBI36
NG_008077.1:g.5281G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251643.5:c.257G>A MANE Select	ENSP00000251643.4:p.Gly86Glu
ENST00000647902.1:c.211+46G>A	ENSP00000497770.1:n.211+46G>A
ENST00000251643.4:c.257G>A	ENSP00000251643.4:p.Gly86Glu
NM_000223.3:c.257G>A	NP_000214.1:p.Gly86Glu
XR_934754.1:n.1500+16070C>T
XR_934754.2:n.2008+16070C>T
NM_000223.4:c.257G>A MANE Select	NP_000214.1:p.Gly86Glu