Canonical Allele Identifier: CA2796088878
Gene: RDH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55722066del , CM000674.2:g.55722066del GRCh38
NC_000012.11:g.56115850del , CM000674.1:g.56115850del GRCh37
NC_000012.10:g.54402117del NCBI36
NG_008606.1:g.6700del

Transcript Alleles

HGVS Amino-acid Change
ENST00000257895.10:c.569+119del MANE Select ENSP00000257895.6:n.569+119del
ENST00000257895.9:c.569+119del ENSP00000257895.5:n.569+119del
ENST00000257899.3:c.591+112del
ENST00000547072.5:c.278+119del ENSP00000449927.1:n.278+119del
ENST00000548082.1:c.569+119del ENSP00000447128.1:n.569+119del
ENST00000548123.1:c.300+572del
ENST00000548486.1:n.698del
ENST00000550412.5:c.*360del ENSP00000447650.1:n.*360del
ENST00000550608.1:n.827del
ENST00000551946.5:c.*491del ENSP00000450201.1:n.*491del
ENST00000553160.1:n.406-129del
NM_001199771.1:c.569+119del NP_001186700.1:n.569+119del
NM_002905.3:c.569+119del NP_002896.2:n.569+119del
NR_037658.1:n.628+119del
NM_001199771.2:c.569+119del NP_001186700.1:n.569+119del
NM_002905.5:c.569+119del MANE Select NP_002896.2:n.569+119del
NM_001199771.3:c.569+119del NP_001186700.1:n.569+119del