Canonical Allele Identifier: CA2259745901
Gene: KRT12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866966C= , CM000679.2:g.40866966C= GRCh38
NC_000017.10:g.39023218C= , CM000679.1:g.39023218C= GRCh37
NC_000017.9:g.36276744C= NCBI36
NG_008077.1:g.5245G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251643.5:c.221G= MANE Select ENSP00000251643.4:p.Gly74=
ENST00000647902.1:c.211+10G= ENSP00000497770.1:n.211+10G=
ENST00000251643.4:c.221G= ENSP00000251643.4:p.Gly74=
NM_000223.3:c.221G= NP_000214.1:p.Gly74=
XR_934754.1:n.1500+16106C=
XR_934754.2:n.2008+16106C=
NM_000223.4:c.221G= MANE Select NP_000214.1:p.Gly74=