Canonical Allele Identifier: CA2259745980
Gene: KRT12 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.37C= MANE Select ENSP00000251643.4:p.Arg13=
ENST00000647902.1:c.37C= ENSP00000497770.1:p.Arg13=
ENST00000251643.4:c.37C= ENSP00000251643.4:p.Arg13=
NM_000223.3:c.37C= NP_000214.1:p.Arg13=
XR_934754.1:n.1500+16290G=
XR_934754.2:n.2008+16290G=
NM_000223.4:c.37C= MANE Select NP_000214.1:p.Arg13=