Canonical Allele Identifier: CA384923673
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516697T>A , CM000674.2:g.52516697T>A GRCh38
NC_000012.11:g.52910481T>A , CM000674.1:g.52910481T>A GRCh37
NC_000012.10:g.51196748T>A NCBI36
NG_008297.1:g.8763A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1379A>T MANE Select ENSP00000252242.4:p.Lys460Met
ENST00000252242.8:c.1379A>T ENSP00000252242.4:p.Lys460Met
ENST00000547890.5:n.757A>T
ENST00000548409.5:c.501A>T
ENST00000549511.5:n.586A>T
ENST00000552629.5:n.1477A>T
NM_000424.3:c.1379A>T NP_000415.2:p.Lys460Met
NM_000424.4:c.1379A>T MANE Select NP_000415.2:p.Lys460Met