Canonical Allele Identifier: CA2619204951

Gene: RDH5

Linked Data

• gnomAD v4: 12-55722045-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55722045T>A , CM000674.2:g.55722045T>A	GRCh38
NC_000012.11:g.56115829T>A , CM000674.1:g.56115829T>A	GRCh37
NC_000012.10:g.54402096T>A	NCBI36
NG_008606.1:g.6679T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.569+98T>A MANE Select	ENSP00000257895.6:n.569+98T>A
ENST00000257895.9:c.569+98T>A	ENSP00000257895.5:n.569+98T>A
ENST00000257899.3:c.591+91T>A
ENST00000547072.5:c.278+98T>A	ENSP00000449927.1:n.278+98T>A
ENST00000548082.1:c.569+98T>A	ENSP00000447128.1:n.569+98T>A
ENST00000548123.1:c.300+551T>A
ENST00000548486.1:n.677T>A
ENST00000550412.5:c.*339T>A	ENSP00000447650.1:n.*339T>A
ENST00000550608.1:n.806T>A
ENST00000551946.5:c.*470T>A	ENSP00000450201.1:n.*470T>A
ENST00000553160.1:n.406-150T>A
NM_001199771.1:c.569+98T>A	NP_001186700.1:n.569+98T>A
NM_002905.3:c.569+98T>A	NP_002896.2:n.569+98T>A
NR_037658.1:n.628+98T>A
NM_001199771.2:c.569+98T>A	NP_001186700.1:n.569+98T>A
NM_002905.5:c.569+98T>A MANE Select	NP_002896.2:n.569+98T>A
NM_001199771.3:c.569+98T>A	NP_001186700.1:n.569+98T>A