Canonical Allele Identifier: CA385201198

Gene: RDH5

Linked Data

• dbSNP Id: rs1592521741
• MyVariant Identifiers: chr12:g.56115712G>A (hg19) ; chr12:g.55721928G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721928G>A , CM000674.2:g.55721928G>A	GRCh38
NC_000012.11:g.56115712G>A , CM000674.1:g.56115712G>A	GRCh37
NC_000012.10:g.54401979G>A	NCBI36
NG_008606.1:g.6562G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.550G>A MANE Select	ENSP00000257895.6:p.Ala184Thr
ENST00000257895.9:c.550G>A	ENSP00000257895.5:p.Ala184Thr
ENST00000257899.3:c.565G>A
ENST00000547072.5:c.259G>A	ENSP00000449927.1:p.Ala87Thr
ENST00000548082.1:c.550G>A	ENSP00000447128.1:p.Ala184Thr
ENST00000548123.1:c.300+434G>A
ENST00000548486.1:n.560G>A
ENST00000550412.5:c.*222G>A	ENSP00000447650.1:n.*222G>A
ENST00000550608.1:n.689G>A
ENST00000551946.5:c.*353G>A	ENSP00000450201.1:n.*353G>A
ENST00000553160.1:n.406-267G>A
ENST00000553187.5:n.560G>A
NM_001199771.1:c.550G>A	NP_001186700.1:p.Ala184Thr
NM_002905.3:c.550G>A	NP_002896.2:p.Ala184Thr
NR_037658.1:n.609G>A
NM_001199771.2:c.550G>A	NP_001186700.1:p.Ala184Thr
NM_002905.5:c.550G>A MANE Select	NP_002896.2:p.Ala184Thr
NM_001199771.3:c.550G>A	NP_001186700.1:p.Ala184Thr