Canonical Allele Identifier: CA8548980
Gene: KRT12 HGNC NCBI

Linked Data

dbSNP Id: rs745817473

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867150G>A , CM000679.2:g.40867150G>A GRCh38
NC_000017.10:g.39023402G>A , CM000679.1:g.39023402G>A GRCh37
NC_000017.9:g.36276928G>A NCBI36
NG_008077.1:g.5061C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.37C>T MANE Select ENSP00000251643.4:p.Arg13Cys
ENST00000647902.1:c.37C>T ENSP00000497770.1:p.Arg13Cys
ENST00000251643.4:c.37C>T ENSP00000251643.4:p.Arg13Cys
NM_000223.3:c.37C>T NP_000214.1:p.Arg13Cys
XR_934754.1:n.1500+16290G>A
XR_934754.2:n.2008+16290G>A
NM_000223.4:c.37C>T MANE Select NP_000214.1:p.Arg13Cys