Canonical Allele Identifier: CA645584190
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519950_52519951insA , CM000674.2:g.52519950_52519951insA GRCh38
NC_000012.11:g.52913734_52913735insA , CM000674.1:g.52913734_52913735insA GRCh37
NC_000012.10:g.51200001_51200002insA NCBI36
NG_008297.1:g.5509_5510insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.346_347insT MANE Select ENSP00000252242.4:p.Gly116ValfsTer?
ENST00000252242.8:c.346_347insT ENSP00000252242.4:p.Gly116ValfsTer?
ENST00000546577.1:c.346_347insT ENSP00000449651.1:p.Gly116ValfsTer?
ENST00000549420.1:c.44-28_44-27insT ENSP00000447209.1:n.44-28_44-27insT
ENST00000551275.1:c.241_242insT ENSP00000448041.1:p.Gly81ValfsTer?
ENST00000552629.5:n.444_445insT
NM_000424.3:c.346_347insT NP_000415.2:p.Gly116ValfsTer?
NM_000424.4:c.346_347insT MANE Select NP_000415.2:p.Gly116ValfsTer?