Canonical Allele Identifier: CA2036538962
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516736G= , CM000674.2:g.52516736G= GRCh38
NC_000012.11:g.52910520G= , CM000674.1:g.52910520G= GRCh37
NC_000012.10:g.51196787G= NCBI36
NG_008297.1:g.8724C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1340C= MANE Select ENSP00000252242.4:p.Ala447=
ENST00000252242.8:c.1340C= ENSP00000252242.4:p.Ala447=
ENST00000547890.5:n.718C=
ENST00000548409.5:c.462C=
ENST00000549511.5:n.547C=
ENST00000552629.5:n.1438C=
NM_000424.3:c.1340C= NP_000415.2:p.Ala447=
NM_000424.4:c.1340C= MANE Select NP_000415.2:p.Ala447=