Canonical Allele Identifier: CA2036538959
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516733C= , CM000674.2:g.52516733C= GRCh38
NC_000012.11:g.52910517C= , CM000674.1:g.52910517C= GRCh37
NC_000012.10:g.51196784C= NCBI36
NG_008297.1:g.8727G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1343G= MANE Select ENSP00000252242.4:p.Arg448=
ENST00000252242.8:c.1343G= ENSP00000252242.4:p.Arg448=
ENST00000547890.5:n.721G=
ENST00000548409.5:c.465G=
ENST00000549511.5:n.550G=
ENST00000552629.5:n.1441G=
NM_000424.3:c.1343G= NP_000415.2:p.Arg448=
NM_000424.4:c.1343G= MANE Select NP_000415.2:p.Arg448=