Canonical Allele Identifier: CA2259745963
Gene: KRT12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867120A= , CM000679.2:g.40867120A= GRCh38
NC_000017.10:g.39023372A= , CM000679.1:g.39023372A= GRCh37
NC_000017.9:g.36276898A= NCBI36
NG_008077.1:g.5091T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.67T= MANE Select ENSP00000251643.4:p.Ser23=
ENST00000647902.1:c.67T= ENSP00000497770.1:p.Ser23=
ENST00000251643.4:c.67T= ENSP00000251643.4:p.Ser23=
NM_000223.3:c.67T= NP_000214.1:p.Ser23=
XR_934754.1:n.1500+16260A=
XR_934754.2:n.2008+16260A=
NM_000223.4:c.67T= MANE Select NP_000214.1:p.Ser23=