Canonical Allele Identifier: CA2259745922
Gene: KRT12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867019G= , CM000679.2:g.40867019G= GRCh38
NC_000017.10:g.39023271G= , CM000679.1:g.39023271G= GRCh37
NC_000017.9:g.36276797G= NCBI36
NG_008077.1:g.5192C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.168C= MANE Select ENSP00000251643.4:p.Gly56=
ENST00000647902.1:c.168C= ENSP00000497770.1:p.Gly56=
ENST00000251643.4:c.168C= ENSP00000251643.4:p.Gly56=
NM_000223.3:c.168C= NP_000214.1:p.Gly56=
XR_934754.1:n.1500+16159G=
XR_934754.2:n.2008+16159G=
NM_000223.4:c.168C= MANE Select NP_000214.1:p.Gly56=