Canonical Allele Identifier: CA2038069365
Gene: RDH5 HGNC NCBI

Linked Data

dbSNP Id: rs1876922534

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55721613del , CM000674.2:g.55721613del GRCh38
NC_000012.11:g.56115397del , CM000674.1:g.56115397del GRCh37
NC_000012.10:g.54401664del NCBI36
NG_008606.1:g.6247del

Transcript Alleles

HGVS Amino-acid Change
ENST00000257895.10:c.311-76del MANE Select ENSP00000257895.6:n.311-76del
ENST00000257895.9:c.311-76del ENSP00000257895.5:n.311-76del
ENST00000257899.3:c.326-76del
ENST00000547072.5:c.20-76del ENSP00000449927.1:n.20-76del
ENST00000547301.1:n.343del
ENST00000548082.1:c.311-76del ENSP00000447128.1:n.311-76del
ENST00000548123.1:c.300+119del
ENST00000548486.1:n.321-76del
ENST00000549424.1:c.118-76del ENSP00000447621.1:n.118-76del
ENST00000550412.5:c.352-76del ENSP00000447650.1:n.352-76del
ENST00000550608.1:n.450-76del
ENST00000551946.5:c.*114-76del ENSP00000450201.1:n.*114-76del
ENST00000552930.5:c.20-76del ENSP00000448014.1:n.20-76del
ENST00000553160.1:n.406-582del
ENST00000553187.5:n.321-76del
NM_001199771.1:c.311-76del NP_001186700.1:n.311-76del
NM_002905.3:c.311-76del NP_002896.2:n.311-76del
NR_037658.1:n.370-76del
NM_001199771.2:c.311-76del NP_001186700.1:n.311-76del
NM_002905.5:c.311-76del MANE Select NP_002896.2:n.311-76del
NM_001199771.3:c.311-76del NP_001186700.1:n.311-76del