Canonical Allele Identifier: CA385201015
Gene: RDH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55721866G>T , CM000674.2:g.55721866G>T GRCh38
NC_000012.11:g.56115650G>T , CM000674.1:g.56115650G>T GRCh37
NC_000012.10:g.54401917G>T NCBI36
NG_008606.1:g.6500G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000257895.10:c.488G>T MANE Select ENSP00000257895.6:p.Ser163Ile
ENST00000257895.9:c.488G>T ENSP00000257895.5:p.Ser163Ile
ENST00000257899.3:c.503G>T
ENST00000547072.5:c.197G>T ENSP00000449927.1:p.Ser66Ile
ENST00000548082.1:c.488G>T ENSP00000447128.1:p.Ser163Ile
ENST00000548123.1:c.300+372G>T
ENST00000548486.1:n.498G>T
ENST00000550412.5:c.*160G>T ENSP00000447650.1:n.*160G>T
ENST00000550608.1:n.627G>T
ENST00000551946.5:c.*291G>T ENSP00000450201.1:n.*291G>T
ENST00000553160.1:n.406-329G>T
ENST00000553187.5:n.498G>T
NM_001199771.1:c.488G>T NP_001186700.1:p.Ser163Ile
NM_002905.3:c.488G>T NP_002896.2:p.Ser163Ile
NR_037658.1:n.547G>T
NM_001199771.2:c.488G>T NP_001186700.1:p.Ser163Ile
NM_002905.5:c.488G>T MANE Select NP_002896.2:p.Ser163Ile
NM_001199771.3:c.488G>T NP_001186700.1:p.Ser163Ile