Canonical Allele Identifier: CA2036540499
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519882C= , CM000674.2:g.52519882C= GRCh38
NC_000012.11:g.52913666C= , CM000674.1:g.52913666C= GRCh37
NC_000012.10:g.51199933C= NCBI36
NG_008297.1:g.5578G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.415G= MANE Select ENSP00000252242.4:p.Gly139=
ENST00000252242.8:c.415G= ENSP00000252242.4:p.Gly139=
ENST00000549420.1:c.85G= ENSP00000447209.1:p.Gly29=
ENST00000551275.1:c.310G= ENSP00000448041.1:p.Gly104=
ENST00000552629.5:n.513G=
NM_000424.3:c.415G= NP_000415.2:p.Gly139=
NM_000424.4:c.415G= MANE Select NP_000415.2:p.Gly139=