Canonical Allele Identifier: CA2259745935
Gene: KRT12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867058C= , CM000679.2:g.40867058C= GRCh38
NC_000017.10:g.39023310C= , CM000679.1:g.39023310C= GRCh37
NC_000017.9:g.36276836C= NCBI36
NG_008077.1:g.5153G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.129G= MANE Select ENSP00000251643.4:p.Gly43=
ENST00000647902.1:c.129G= ENSP00000497770.1:p.Gly43=
ENST00000251643.4:c.129G= ENSP00000251643.4:p.Gly43=
NM_000223.3:c.129G= NP_000214.1:p.Gly43=
XR_934754.1:n.1500+16198C=
XR_934754.2:n.2008+16198C=
NM_000223.4:c.129G= MANE Select NP_000214.1:p.Gly43=