Canonical Allele Identifier: CA2036538951
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516720C= , CM000674.2:g.52516720C= GRCh38
NC_000012.11:g.52910504C= , CM000674.1:g.52910504C= GRCh37
NC_000012.10:g.51196771C= NCBI36
NG_008297.1:g.8740G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1356G= MANE Select ENSP00000252242.4:p.Glu452=
ENST00000252242.8:c.1356G= ENSP00000252242.4:p.Glu452=
ENST00000547890.5:n.734G=
ENST00000548409.5:c.478G=
ENST00000549511.5:n.563G=
ENST00000552629.5:n.1454G=
NM_000424.3:c.1356G= NP_000415.2:p.Glu452=
NM_000424.4:c.1356G= MANE Select NP_000415.2:p.Glu452=