Canonical Allele Identifier: CA2036540503
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519891G= , CM000674.2:g.52519891G= GRCh38
NC_000012.11:g.52913675G= , CM000674.1:g.52913675G= GRCh37
NC_000012.10:g.51199942G= NCBI36
NG_008297.1:g.5569C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.406C= MANE Select ENSP00000252242.4:p.Pro136=
ENST00000252242.8:c.406C= ENSP00000252242.4:p.Pro136=
ENST00000549420.1:c.76C= ENSP00000447209.1:p.Pro26=
ENST00000551275.1:c.301C= ENSP00000448041.1:p.Pro101=
ENST00000552629.5:n.504C=
NM_000424.3:c.406C= NP_000415.2:p.Pro136=
NM_000424.4:c.406C= MANE Select NP_000415.2:p.Pro136=