Canonical Allele Identifier: CA124171
Gene: KRT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 14647
dbSNP Id: rs58751565

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520283G>T , CM000674.2:g.52520283G>T GRCh38
NC_000012.11:g.52914067G>T , CM000674.1:g.52914067G>T GRCh37
NC_000012.10:g.51200334G>T NCBI36
NG_008297.1:g.5177C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.14C>A MANE Select ENSP00000252242.4:p.Ser5Ter
ENST00000252242.8:c.14C>A ENSP00000252242.4:p.Ser5Ter
ENST00000546577.1:c.14C>A ENSP00000449651.1:p.Ser5Ter
ENST00000549420.1:c.14C>A ENSP00000447209.1:p.Ser5Ter
ENST00000551275.1:c.14C>A ENSP00000448041.1:p.Ser5Ter
ENST00000552629.5:n.112C>A
NM_000424.3:c.14C>A NP_000415.2:p.Ser5Ter
NM_000424.4:c.14C>A MANE Select NP_000415.2:p.Ser5Ter