Canonical Allele Identifier: CA385200576
Gene: RDH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55721708T>A , CM000674.2:g.55721708T>A GRCh38
NC_000012.11:g.56115492T>A , CM000674.1:g.56115492T>A GRCh37
NC_000012.10:g.54401759T>A NCBI36
NG_008606.1:g.6342T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000257895.10:c.330T>A MANE Select ENSP00000257895.6:p.Asn110Lys
ENST00000257895.9:c.330T>A ENSP00000257895.5:p.Asn110Lys
ENST00000257899.3:c.345T>A
ENST00000547072.5:c.39T>A ENSP00000449927.1:p.Asn13Lys
ENST00000547301.1:n.438T>A
ENST00000548082.1:c.330T>A ENSP00000447128.1:p.Asn110Lys
ENST00000548123.1:c.300+214T>A
ENST00000548486.1:n.340T>A
ENST00000549424.1:c.*2T>A ENSP00000447621.1:n.*2T>A
ENST00000550412.5:c.*2T>A ENSP00000447650.1:n.*2T>A
ENST00000550608.1:n.469T>A
ENST00000551946.5:c.*133T>A ENSP00000450201.1:n.*133T>A
ENST00000552930.5:c.39T>A ENSP00000448014.1:p.Asn13Lys
ENST00000553160.1:n.406-487T>A
ENST00000553187.5:n.340T>A
NM_001199771.1:c.330T>A NP_001186700.1:p.Asn110Lys
NM_002905.3:c.330T>A NP_002896.2:p.Asn110Lys
NR_037658.1:n.389T>A
NM_001199771.2:c.330T>A NP_001186700.1:p.Asn110Lys
NM_002905.5:c.330T>A MANE Select NP_002896.2:p.Asn110Lys
NM_001199771.3:c.330T>A NP_001186700.1:p.Asn110Lys