Canonical Allele Identifier: CA2259745793
Gene: KRT12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866720T= , CM000679.2:g.40866720T= GRCh38
NC_000017.10:g.39022972T= , CM000679.1:g.39022972T= GRCh37
NC_000017.9:g.36276498T= NCBI36
NG_008077.1:g.5491A=

Transcript Alleles

HGVS Amino-acid change
ENST00000251643.5:c.467A= MANE Select ENSP00000251643.4:p.Lys156=
ENST00000647902.1:c.359A= ENSP00000497770.1:p.Lys120=
ENST00000251643.4:c.467A= ENSP00000251643.4:p.Lys156=
NM_000223.3:c.467A= NP_000214.1:p.Lys156=
XR_934754.1:n.1500+15860T=
XR_934754.2:n.2008+15860T=
NM_000223.4:c.467A= MANE Select NP_000214.1:p.Lys156=