Canonical Allele Identifier: CA2038069369

Gene: RDH5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721619G= , CM000674.2:g.55721619G=	GRCh38
NC_000012.11:g.56115403G= , CM000674.1:g.56115403G=	GRCh37
NC_000012.10:g.54401670G=	NCBI36
NG_008606.1:g.6253G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.311-70G= MANE Select	ENSP00000257895.6:n.311-70G=
ENST00000257895.9:c.311-70G=	ENSP00000257895.5:n.311-70G=
ENST00000257899.3:c.326-70G=
ENST00000547072.5:c.20-70G=	ENSP00000449927.1:n.20-70G=
ENST00000547301.1:n.349G=
ENST00000548082.1:c.311-70G=	ENSP00000447128.1:n.311-70G=
ENST00000548123.1:c.300+125G=
ENST00000548486.1:n.321-70G=
ENST00000549424.1:c.118-70G=	ENSP00000447621.1:n.118-70G=
ENST00000550412.5:c.352-70G=	ENSP00000447650.1:n.352-70G=
ENST00000550608.1:n.450-70G=
ENST00000551946.5:c.*114-70G=	ENSP00000450201.1:n.*114-70G=
ENST00000552930.5:c.20-70G=	ENSP00000448014.1:n.20-70G=
ENST00000553160.1:n.406-576G=
ENST00000553187.5:n.321-70G=
NM_001199771.1:c.311-70G=	NP_001186700.1:n.311-70G=
NM_002905.3:c.311-70G=	NP_002896.2:n.311-70G=
NR_037658.1:n.370-70G=
NM_001199771.2:c.311-70G=	NP_001186700.1:n.311-70G=
NM_002905.5:c.311-70G= MANE Select	NP_002896.2:n.311-70G=
NM_001199771.3:c.311-70G=	NP_001186700.1:n.311-70G=