Canonical Allele Identifier: CA385200536

Gene: RDH5

Linked Data

• gnomAD v4: 12-55721698-G-A
• MyVariant Identifiers: chr12:g.56115482G>A (hg19) ; chr12:g.55721698G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721698G>A , CM000674.2:g.55721698G>A	GRCh38
NC_000012.11:g.56115482G>A , CM000674.1:g.56115482G>A	GRCh37
NC_000012.10:g.54401749G>A	NCBI36
NG_008606.1:g.6332G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.320G>A MANE Select	ENSP00000257895.6:p.Gly107Asp
ENST00000257895.9:c.320G>A	ENSP00000257895.5:p.Gly107Asp
ENST00000257899.3:c.335G>A
ENST00000547072.5:c.29G>A	ENSP00000449927.1:p.Gly10Asp
ENST00000547301.1:n.428G>A
ENST00000548082.1:c.320G>A	ENSP00000447128.1:p.Gly107Asp
ENST00000548123.1:c.300+204G>A
ENST00000548486.1:n.330G>A
ENST00000549424.1:c.127G>A	ENSP00000447621.1:p.Val43Ile
ENST00000550412.5:c.361G>A	ENSP00000447650.1:p.Val121Ile
ENST00000550608.1:n.459G>A
ENST00000551946.5:c.*123G>A	ENSP00000450201.1:n.*123G>A
ENST00000552930.5:c.29G>A	ENSP00000448014.1:p.Gly10Asp
ENST00000553160.1:n.406-497G>A
ENST00000553187.5:n.330G>A
NM_001199771.1:c.320G>A	NP_001186700.1:p.Gly107Asp
NM_002905.3:c.320G>A	NP_002896.2:p.Gly107Asp
NR_037658.1:n.379G>A
NM_001199771.2:c.320G>A	NP_001186700.1:p.Gly107Asp
NM_002905.5:c.320G>A MANE Select	NP_002896.2:p.Gly107Asp
NM_001199771.3:c.320G>A	NP_001186700.1:p.Gly107Asp