Canonical Allele Identifier: CA2575165513
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520263del , CM000674.2:g.52520263del GRCh38
NC_000012.11:g.52914047del , CM000674.1:g.52914047del GRCh37
NC_000012.10:g.51200314del NCBI36
NG_008297.1:g.5201del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.38del MANE Select ENSP00000252242.4:p.Gly13AlafsTer?
ENST00000252242.8:c.38del ENSP00000252242.4:p.Gly13AlafsTer?
ENST00000546577.1:c.38del ENSP00000449651.1:p.Gly13AlafsTer?
ENST00000549420.1:c.38del ENSP00000447209.1:p.Gly13AlafsTer28
ENST00000551275.1:c.38del ENSP00000448041.1:p.Gly13AlafsTer?
ENST00000552629.5:n.136del
NM_000424.3:c.38del NP_000415.2:p.Gly13AlafsTer?
NM_000424.4:c.38del MANE Select NP_000415.2:p.Gly13AlafsTer?