Canonical Allele Identifier: CA2038069514
Gene: RDH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55721914A= , CM000674.2:g.55721914A= GRCh38
NC_000012.11:g.56115698A= , CM000674.1:g.56115698A= GRCh37
NC_000012.10:g.54401965A= NCBI36
NG_008606.1:g.6548A=

Transcript Alleles

HGVS Amino-acid change
ENST00000257895.10:c.536A= MANE Select ENSP00000257895.6:p.Lys179=
ENST00000257895.9:c.536A= ENSP00000257895.5:p.Lys179=
ENST00000257899.3:c.551A=
ENST00000547072.5:c.245A= ENSP00000449927.1:p.Lys82=
ENST00000548082.1:c.536A= ENSP00000447128.1:p.Lys179=
ENST00000548123.1:c.300+420A=
ENST00000548486.1:n.546A=
ENST00000550412.5:c.*208A= ENSP00000447650.1:n.*208A=
ENST00000550608.1:n.675A=
ENST00000551946.5:c.*339A= ENSP00000450201.1:n.*339A=
ENST00000553160.1:n.406-281A=
ENST00000553187.5:n.546A=
NM_001199771.1:c.536A= NP_001186700.1:p.Lys179=
NM_002905.3:c.536A= NP_002896.2:p.Lys179=
NR_037658.1:n.595A=
NM_001199771.2:c.536A= NP_001186700.1:p.Lys179=
NM_002905.5:c.536A= MANE Select NP_002896.2:p.Lys179=
NM_001199771.3:c.536A= NP_001186700.1:p.Lys179=