Canonical Allele Identifier: CA2619208729
Gene: RDH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55721672T>C , CM000674.2:g.55721672T>C GRCh38
NC_000012.11:g.56115456T>C , CM000674.1:g.56115456T>C GRCh37
NC_000012.10:g.54401723T>C NCBI36
NG_008606.1:g.6306T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000257895.10:c.311-17T>C MANE Select ENSP00000257895.6:n.311-17T>C
ENST00000257895.9:c.311-17T>C ENSP00000257895.5:n.311-17T>C
ENST00000257899.3:c.326-17T>C
ENST00000547072.5:c.20-17T>C ENSP00000449927.1:n.20-17T>C
ENST00000547301.1:n.402T>C
ENST00000548082.1:c.311-17T>C ENSP00000447128.1:n.311-17T>C
ENST00000548123.1:c.300+178T>C
ENST00000548486.1:n.321-17T>C
ENST00000549424.1:c.118-17T>C ENSP00000447621.1:n.118-17T>C
ENST00000550412.5:c.352-17T>C ENSP00000447650.1:n.352-17T>C
ENST00000550608.1:n.450-17T>C
ENST00000551946.5:c.*114-17T>C ENSP00000450201.1:n.*114-17T>C
ENST00000552930.5:c.20-17T>C ENSP00000448014.1:n.20-17T>C
ENST00000553160.1:n.406-523T>C
ENST00000553187.5:n.321-17T>C
NM_001199771.1:c.311-17T>C NP_001186700.1:n.311-17T>C
NM_002905.3:c.311-17T>C NP_002896.2:n.311-17T>C
NR_037658.1:n.370-17T>C
NM_001199771.2:c.311-17T>C NP_001186700.1:n.311-17T>C
NM_002905.5:c.311-17T>C MANE Select NP_002896.2:n.311-17T>C
NM_001199771.3:c.311-17T>C NP_001186700.1:n.311-17T>C