Canonical Allele Identifier: CA385200600
Gene: RDH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55721715G>A , CM000674.2:g.55721715G>A GRCh38
NC_000012.11:g.56115499G>A , CM000674.1:g.56115499G>A GRCh37
NC_000012.10:g.54401766G>A NCBI36
NG_008606.1:g.6349G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000257895.10:c.337G>A MANE Select ENSP00000257895.6:p.Gly113Ser
ENST00000257895.9:c.337G>A ENSP00000257895.5:p.Gly113Ser
ENST00000257899.3:c.352G>A
ENST00000547072.5:c.46G>A ENSP00000449927.1:p.Gly16Ser
ENST00000547301.1:n.445G>A
ENST00000548082.1:c.337G>A ENSP00000447128.1:p.Gly113Ser
ENST00000548123.1:c.300+221G>A
ENST00000548486.1:n.347G>A
ENST00000549424.1:c.*9G>A ENSP00000447621.1:n.*9G>A
ENST00000550412.5:c.*9G>A ENSP00000447650.1:n.*9G>A
ENST00000550608.1:n.476G>A
ENST00000551946.5:c.*140G>A ENSP00000450201.1:n.*140G>A
ENST00000552930.5:c.46G>A ENSP00000448014.1:p.Gly16Ser
ENST00000553160.1:n.406-480G>A
ENST00000553187.5:n.347G>A
NM_001199771.1:c.337G>A NP_001186700.1:p.Gly113Ser
NM_002905.3:c.337G>A NP_002896.2:p.Gly113Ser
NR_037658.1:n.396G>A
NM_001199771.2:c.337G>A NP_001186700.1:p.Gly113Ser
NM_002905.5:c.337G>A MANE Select NP_002896.2:p.Gly113Ser
NM_001199771.3:c.337G>A NP_001186700.1:p.Gly113Ser