Canonical Allele Identifier: CA2036538942
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516696C= , CM000674.2:g.52516696C= GRCh38
NC_000012.11:g.52910480C= , CM000674.1:g.52910480C= GRCh37
NC_000012.10:g.51196747C= NCBI36
NG_008297.1:g.8764G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1380G= MANE Select ENSP00000252242.4:p.Lys460=
ENST00000252242.8:c.1380G= ENSP00000252242.4:p.Lys460=
ENST00000547890.5:n.758G=
ENST00000548409.5:c.502G=
ENST00000549511.5:n.587G=
ENST00000552629.5:n.1478G=
NM_000424.3:c.1380G= NP_000415.2:p.Lys460=
NM_000424.4:c.1380G= MANE Select NP_000415.2:p.Lys460=