Canonical Allele Identifier: CA384930865
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs1170652770

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520175C>T , CM000674.2:g.52520175C>T GRCh38
NC_000012.11:g.52913959C>T , CM000674.1:g.52913959C>T GRCh37
NC_000012.10:g.51200226C>T NCBI36
NG_008297.1:g.5285G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.122G>A MANE Select ENSP00000252242.4:p.Gly41Asp
ENST00000252242.8:c.122G>A ENSP00000252242.4:p.Gly41Asp
ENST00000546577.1:c.122G>A ENSP00000449651.1:p.Gly41Asp
ENST00000549420.1:c.43+79G>A ENSP00000447209.1:n.43+79G>A
ENST00000551275.1:c.122G>A ENSP00000448041.1:p.Gly41Asp
ENST00000552629.5:n.220G>A
NM_000424.3:c.122G>A NP_000415.2:p.Gly41Asp
NM_000424.4:c.122G>A MANE Select NP_000415.2:p.Gly41Asp