Canonical Allele Identifier: CA2038069482

Gene: RDH5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721844G= , CM000674.2:g.55721844G=	GRCh38
NC_000012.11:g.56115628G= , CM000674.1:g.56115628G=	GRCh37
NC_000012.10:g.54401895G=	NCBI36
NG_008606.1:g.6478G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.466G= MANE Select	ENSP00000257895.6:p.Gly156=
ENST00000257895.9:c.466G=	ENSP00000257895.5:p.Gly156=
ENST00000257899.3:c.481G=
ENST00000547072.5:c.175G=	ENSP00000449927.1:p.Gly59=
ENST00000548082.1:c.466G=	ENSP00000447128.1:p.Gly156=
ENST00000548123.1:c.300+350G=
ENST00000548486.1:n.476G=
ENST00000550412.5:c.*138G=	ENSP00000447650.1:n.*138G=
ENST00000550608.1:n.605G=
ENST00000551946.5:c.*269G=	ENSP00000450201.1:n.*269G=
ENST00000553160.1:n.406-351G=
ENST00000553187.5:n.476G=
NM_001199771.1:c.466G=	NP_001186700.1:p.Gly156=
NM_002905.3:c.466G=	NP_002896.2:p.Gly156=
NR_037658.1:n.525G=
NM_001199771.2:c.466G=	NP_001186700.1:p.Gly156=
NM_002905.5:c.466G= MANE Select	NP_002896.2:p.Gly156=
NM_001199771.3:c.466G=	NP_001186700.1:p.Gly156=