Canonical Allele Identifier: CA2036540074
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519033C= , CM000674.2:g.52519033C= GRCh38
NC_000012.11:g.52912817C= , CM000674.1:g.52912817C= GRCh37
NC_000012.10:g.51199084C= NCBI36
NG_008297.1:g.6427G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.683G= MANE Select ENSP00000252242.4:p.Arg228=
ENST00000252242.8:c.683G= ENSP00000252242.4:p.Arg228=
ENST00000549420.1:c.353G= ENSP00000447209.1:p.Arg118=
ENST00000551013.1:n.211G=
ENST00000551188.5:c.85G=
ENST00000552629.5:n.781G=
NM_000424.3:c.683G= NP_000415.2:p.Arg228=
NM_000424.4:c.683G= MANE Select NP_000415.2:p.Arg228=