Canonical Allele Identifier: CA2259745903
Gene: KRT12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866968G= , CM000679.2:g.40866968G= GRCh38
NC_000017.10:g.39023220G= , CM000679.1:g.39023220G= GRCh37
NC_000017.9:g.36276746G= NCBI36
NG_008077.1:g.5243C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.219C= MANE Select ENSP00000251643.4:p.Ser73=
ENST00000647902.1:c.211+8C= ENSP00000497770.1:n.211+8C=
ENST00000251643.4:c.219C= ENSP00000251643.4:p.Ser73=
NM_000223.3:c.219C= NP_000214.1:p.Ser73=
XR_934754.1:n.1500+16108G=
XR_934754.2:n.2008+16108G=
NM_000223.4:c.219C= MANE Select NP_000214.1:p.Ser73=