Canonical Allele Identifier: CA2619204790

Gene: RDH5

Linked Data

• gnomAD v4: 12-55721972-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721972C>A , CM000674.2:g.55721972C>A	GRCh38
NC_000012.11:g.56115756C>A , CM000674.1:g.56115756C>A	GRCh37
NC_000012.10:g.54402023C>A	NCBI36
NG_008606.1:g.6606C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.569+25C>A MANE Select	ENSP00000257895.6:n.569+25C>A
ENST00000257895.9:c.569+25C>A	ENSP00000257895.5:n.569+25C>A
ENST00000257899.3:c.591+18C>A
ENST00000547072.5:c.278+25C>A	ENSP00000449927.1:n.278+25C>A
ENST00000548082.1:c.569+25C>A	ENSP00000447128.1:n.569+25C>A
ENST00000548123.1:c.300+478C>A
ENST00000548486.1:n.604C>A
ENST00000550412.5:c.*266C>A	ENSP00000447650.1:n.*266C>A
ENST00000550608.1:n.733C>A
ENST00000551946.5:c.*397C>A	ENSP00000450201.1:n.*397C>A
ENST00000553160.1:n.406-223C>A
ENST00000553187.5:n.604C>A
NM_001199771.1:c.569+25C>A	NP_001186700.1:n.569+25C>A
NM_002905.3:c.569+25C>A	NP_002896.2:n.569+25C>A
NR_037658.1:n.628+25C>A
NM_001199771.2:c.569+25C>A	NP_001186700.1:n.569+25C>A
NM_002905.5:c.569+25C>A MANE Select	NP_002896.2:n.569+25C>A
NM_001199771.3:c.569+25C>A	NP_001186700.1:n.569+25C>A