Canonical Allele Identifier: CA384924125
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516783C>A , CM000674.2:g.52516783C>A GRCh38
NC_000012.11:g.52910567C>A , CM000674.1:g.52910567C>A GRCh37
NC_000012.10:g.51196834C>A NCBI36
NG_008297.1:g.8677G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1293G>T MANE Select ENSP00000252242.4:p.Lys431Asn
ENST00000252242.8:c.1293G>T ENSP00000252242.4:p.Lys431Asn
ENST00000547890.5:n.671G>T
ENST00000548409.5:c.415G>T
ENST00000549511.5:n.500G>T
ENST00000552629.5:n.1391G>T
NM_000424.3:c.1293G>T NP_000415.2:p.Lys431Asn
NM_000424.4:c.1293G>T MANE Select NP_000415.2:p.Lys431Asn