Canonical Allele Identifier: CA2809477252
Gene: KRT12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866991del , CM000679.2:g.40866991del GRCh38
NC_000017.10:g.39023243del , CM000679.1:g.39023243del GRCh37
NC_000017.9:g.36276769del NCBI36
NG_008077.1:g.5220del

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.196del MANE Select ENSP00000251643.4:p.Ser66ValfsTer?
ENST00000647902.1:c.196del ENSP00000497770.1:p.Ser66ValfsTer9
ENST00000251643.4:c.196del ENSP00000251643.4:p.Ser66ValfsTer?
NM_000223.3:c.196del NP_000214.1:p.Ser66ValfsTer?
XR_934754.1:n.1500+16131del
XR_934754.2:n.2008+16131del
NM_000223.4:c.196del MANE Select NP_000214.1:p.Ser66ValfsTer?