Canonical Allele Identifier: CA690144152

Gene: RDH5

Linked Data

• dbSNP Id: rs1192346533
• gnomAD v3: 12-55721636-G-A
• gnomAD v4: 12-55721636-G-A
• MyVariant Identifiers: chr12:g.56115420G>A (hg19) ; chr12:g.55721636G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721636G>A , CM000674.2:g.55721636G>A	GRCh38
NC_000012.11:g.56115420G>A , CM000674.1:g.56115420G>A	GRCh37
NC_000012.10:g.54401687G>A	NCBI36
NG_008606.1:g.6270G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.311-53G>A MANE Select	ENSP00000257895.6:n.311-53G>A
ENST00000257895.9:c.311-53G>A	ENSP00000257895.5:n.311-53G>A
ENST00000257899.3:c.326-53G>A
ENST00000547072.5:c.20-53G>A	ENSP00000449927.1:n.20-53G>A
ENST00000547301.1:n.366G>A
ENST00000548082.1:c.311-53G>A	ENSP00000447128.1:n.311-53G>A
ENST00000548123.1:c.300+142G>A
ENST00000548486.1:n.321-53G>A
ENST00000549424.1:c.118-53G>A	ENSP00000447621.1:n.118-53G>A
ENST00000550412.5:c.352-53G>A	ENSP00000447650.1:n.352-53G>A
ENST00000550608.1:n.450-53G>A
ENST00000551946.5:c.*114-53G>A	ENSP00000450201.1:n.*114-53G>A
ENST00000552930.5:c.20-53G>A	ENSP00000448014.1:n.20-53G>A
ENST00000553160.1:n.406-559G>A
ENST00000553187.5:n.321-53G>A
NM_001199771.1:c.311-53G>A	NP_001186700.1:n.311-53G>A
NM_002905.3:c.311-53G>A	NP_002896.2:n.311-53G>A
NR_037658.1:n.370-53G>A
NM_001199771.2:c.311-53G>A	NP_001186700.1:n.311-53G>A
NM_002905.5:c.311-53G>A MANE Select	NP_002896.2:n.311-53G>A
NM_001199771.3:c.311-53G>A	NP_001186700.1:n.311-53G>A