Canonical Allele Identifier: CA2036540472
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519832C= , CM000674.2:g.52519832C= GRCh38
NC_000012.11:g.52913616C= , CM000674.1:g.52913616C= GRCh37
NC_000012.10:g.51199883C= NCBI36
NG_008297.1:g.5628G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.465G= MANE Select ENSP00000252242.4:p.Leu155=
ENST00000252242.8:c.465G= ENSP00000252242.4:p.Leu155=
ENST00000549420.1:c.135G= ENSP00000447209.1:p.Leu45=
ENST00000551275.1:c.360G= ENSP00000448041.1:p.Leu120=
ENST00000552629.5:n.563G=
NM_000424.3:c.465G= NP_000415.2:p.Leu155=
NM_000424.4:c.465G= MANE Select NP_000415.2:p.Leu155=