Canonical Allele Identifier: CA2259745909
Gene: KRT12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866986G= , CM000679.2:g.40866986G= GRCh38
NC_000017.10:g.39023238G= , CM000679.1:g.39023238G= GRCh37
NC_000017.9:g.36276764G= NCBI36
NG_008077.1:g.5225C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.201C= MANE Select ENSP00000251643.4:p.Ser67=
ENST00000647902.1:c.201C= ENSP00000497770.1:p.Ser67=
ENST00000251643.4:c.201C= ENSP00000251643.4:p.Ser67=
NM_000223.3:c.201C= NP_000214.1:p.Ser67=
XR_934754.1:n.1500+16126G=
XR_934754.2:n.2008+16126G=
NM_000223.4:c.201C= MANE Select NP_000214.1:p.Ser67=