Canonical Allele Identifier: CA2619204977

Gene: RDH5

Linked Data

• gnomAD v4: 12-55722060-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55722060T>G , CM000674.2:g.55722060T>G	GRCh38
NC_000012.11:g.56115844T>G , CM000674.1:g.56115844T>G	GRCh37
NC_000012.10:g.54402111T>G	NCBI36
NG_008606.1:g.6694T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.569+113T>G MANE Select	ENSP00000257895.6:n.569+113T>G
ENST00000257895.9:c.569+113T>G	ENSP00000257895.5:n.569+113T>G
ENST00000257899.3:c.591+106T>G
ENST00000547072.5:c.278+113T>G	ENSP00000449927.1:n.278+113T>G
ENST00000548082.1:c.569+113T>G	ENSP00000447128.1:n.569+113T>G
ENST00000548123.1:c.300+566T>G
ENST00000548486.1:n.692T>G
ENST00000550412.5:c.*354T>G	ENSP00000447650.1:n.*354T>G
ENST00000550608.1:n.821T>G
ENST00000551946.5:c.*485T>G	ENSP00000450201.1:n.*485T>G
ENST00000553160.1:n.406-135T>G
NM_001199771.1:c.569+113T>G	NP_001186700.1:n.569+113T>G
NM_002905.3:c.569+113T>G	NP_002896.2:n.569+113T>G
NR_037658.1:n.628+113T>G
NM_001199771.2:c.569+113T>G	NP_001186700.1:n.569+113T>G
NM_002905.5:c.569+113T>G MANE Select	NP_002896.2:n.569+113T>G
NM_001199771.3:c.569+113T>G	NP_001186700.1:n.569+113T>G