Canonical Allele Identifier: CA2259745792
Gene: KRT12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866717A= , CM000679.2:g.40866717A= GRCh38
NC_000017.10:g.39022969A= , CM000679.1:g.39022969A= GRCh37
NC_000017.9:g.36276495A= NCBI36
NG_008077.1:g.5494T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.470T= MANE Select ENSP00000251643.4:p.Ile157=
ENST00000647902.1:c.362T= ENSP00000497770.1:p.Ile121=
ENST00000251643.4:c.470T= ENSP00000251643.4:p.Ile157=
NM_000223.3:c.470T= NP_000214.1:p.Ile157=
XR_934754.1:n.1500+15857A=
XR_934754.2:n.2008+15857A=
NM_000223.4:c.470T= MANE Select NP_000214.1:p.Ile157=