Canonical Allele Identifier: CA2796088879
Gene: RDH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55722068del , CM000674.2:g.55722068del GRCh38
NC_000012.11:g.56115852del , CM000674.1:g.56115852del GRCh37
NC_000012.10:g.54402119del NCBI36
NG_008606.1:g.6702del

Transcript Alleles

HGVS Amino-acid Change
ENST00000257895.10:c.569+121del MANE Select ENSP00000257895.6:n.569+121del
ENST00000257895.9:c.569+121del ENSP00000257895.5:n.569+121del
ENST00000257899.3:c.591+114del
ENST00000547072.5:c.278+121del ENSP00000449927.1:n.278+121del
ENST00000548082.1:c.569+121del ENSP00000447128.1:n.569+121del
ENST00000548123.1:c.300+574del
ENST00000548486.1:n.700del
ENST00000550412.5:c.*362del ENSP00000447650.1:n.*362del
ENST00000550608.1:n.829del
ENST00000551946.5:c.*493del ENSP00000450201.1:n.*493del
ENST00000553160.1:n.406-127del
NM_001199771.1:c.569+121del NP_001186700.1:n.569+121del
NM_002905.3:c.569+121del NP_002896.2:n.569+121del
NR_037658.1:n.628+121del
NM_001199771.2:c.569+121del NP_001186700.1:n.569+121del
NM_002905.5:c.569+121del MANE Select NP_002896.2:n.569+121del
NM_001199771.3:c.569+121del NP_001186700.1:n.569+121del