Canonical Allele Identifier: CA2038069523
Gene: RDH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55721929C= , CM000674.2:g.55721929C= GRCh38
NC_000012.11:g.56115713C= , CM000674.1:g.56115713C= GRCh37
NC_000012.10:g.54401980C= NCBI36
NG_008606.1:g.6563C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257895.10:c.551C= MANE Select ENSP00000257895.6:p.Ala184=
ENST00000257895.9:c.551C= ENSP00000257895.5:p.Ala184=
ENST00000257899.3:c.566C=
ENST00000547072.5:c.260C= ENSP00000449927.1:p.Ala87=
ENST00000548082.1:c.551C= ENSP00000447128.1:p.Ala184=
ENST00000548123.1:c.300+435C=
ENST00000548486.1:n.561C=
ENST00000550412.5:c.*223C= ENSP00000447650.1:n.*223C=
ENST00000550608.1:n.690C=
ENST00000551946.5:c.*354C= ENSP00000450201.1:n.*354C=
ENST00000553160.1:n.406-266C=
ENST00000553187.5:n.561C=
NM_001199771.1:c.551C= NP_001186700.1:p.Ala184=
NM_002905.3:c.551C= NP_002896.2:p.Ala184=
NR_037658.1:n.610C=
NM_001199771.2:c.551C= NP_001186700.1:p.Ala184=
NM_002905.5:c.551C= MANE Select NP_002896.2:p.Ala184=
NM_001199771.3:c.551C= NP_001186700.1:p.Ala184=