Canonical Allele Identifier: CA385201186
Gene: RDH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55721925G>A , CM000674.2:g.55721925G>A GRCh38
NC_000012.11:g.56115709G>A , CM000674.1:g.56115709G>A GRCh37
NC_000012.10:g.54401976G>A NCBI36
NG_008606.1:g.6559G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000257895.10:c.547G>A MANE Select ENSP00000257895.6:p.Glu183Lys
ENST00000257895.9:c.547G>A ENSP00000257895.5:p.Glu183Lys
ENST00000257899.3:c.562G>A
ENST00000547072.5:c.256G>A ENSP00000449927.1:p.Glu86Lys
ENST00000548082.1:c.547G>A ENSP00000447128.1:p.Glu183Lys
ENST00000548123.1:c.300+431G>A
ENST00000548486.1:n.557G>A
ENST00000550412.5:c.*219G>A ENSP00000447650.1:n.*219G>A
ENST00000550608.1:n.686G>A
ENST00000551946.5:c.*350G>A ENSP00000450201.1:n.*350G>A
ENST00000553160.1:n.406-270G>A
ENST00000553187.5:n.557G>A
NM_001199771.1:c.547G>A NP_001186700.1:p.Glu183Lys
NM_002905.3:c.547G>A NP_002896.2:p.Glu183Lys
NR_037658.1:n.606G>A
NM_001199771.2:c.547G>A NP_001186700.1:p.Glu183Lys
NM_002905.5:c.547G>A MANE Select NP_002896.2:p.Glu183Lys
NM_001199771.3:c.547G>A NP_001186700.1:p.Glu183Lys