Canonical Allele Identifier: CA385200683
Gene: RDH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55721747G>T , CM000674.2:g.55721747G>T GRCh38
NC_000012.11:g.56115531G>T , CM000674.1:g.56115531G>T GRCh37
NC_000012.10:g.54401798G>T NCBI36
NG_008606.1:g.6381G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000257895.10:c.369G>T MANE Select ENSP00000257895.6:p.Trp123Cys
ENST00000257895.9:c.369G>T ENSP00000257895.5:p.Trp123Cys
ENST00000257899.3:c.384G>T
ENST00000547072.5:c.78G>T ENSP00000449927.1:p.Trp26Cys
ENST00000547301.1:n.477G>T
ENST00000548082.1:c.369G>T ENSP00000447128.1:p.Trp123Cys
ENST00000548123.1:c.300+253G>T
ENST00000548486.1:n.379G>T
ENST00000549424.1:c.*41G>T ENSP00000447621.1:n.*41G>T
ENST00000550412.5:c.*41G>T ENSP00000447650.1:n.*41G>T
ENST00000550608.1:n.508G>T
ENST00000551946.5:c.*172G>T ENSP00000450201.1:n.*172G>T
ENST00000552930.5:c.78G>T ENSP00000448014.1:p.Trp26Cys
ENST00000553160.1:n.406-448G>T
ENST00000553187.5:n.379G>T
NM_001199771.1:c.369G>T NP_001186700.1:p.Trp123Cys
NM_002905.3:c.369G>T NP_002896.2:p.Trp123Cys
NR_037658.1:n.428G>T
NM_001199771.2:c.369G>T NP_001186700.1:p.Trp123Cys
NM_002905.5:c.369G>T MANE Select NP_002896.2:p.Trp123Cys
NM_001199771.3:c.369G>T NP_001186700.1:p.Trp123Cys