Canonical Allele Identifier: CA2038069370

Gene: RDH5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721620C= , CM000674.2:g.55721620C=	GRCh38
NC_000012.11:g.56115404C= , CM000674.1:g.56115404C=	GRCh37
NC_000012.10:g.54401671C=	NCBI36
NG_008606.1:g.6254C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.311-69C= MANE Select	ENSP00000257895.6:n.311-69C=
ENST00000257895.9:c.311-69C=	ENSP00000257895.5:n.311-69C=
ENST00000257899.3:c.326-69C=
ENST00000547072.5:c.20-69C=	ENSP00000449927.1:n.20-69C=
ENST00000547301.1:n.350C=
ENST00000548082.1:c.311-69C=	ENSP00000447128.1:n.311-69C=
ENST00000548123.1:c.300+126C=
ENST00000548486.1:n.321-69C=
ENST00000549424.1:c.118-69C=	ENSP00000447621.1:n.118-69C=
ENST00000550412.5:c.352-69C=	ENSP00000447650.1:n.352-69C=
ENST00000550608.1:n.450-69C=
ENST00000551946.5:c.*114-69C=	ENSP00000450201.1:n.*114-69C=
ENST00000552930.5:c.20-69C=	ENSP00000448014.1:n.20-69C=
ENST00000553160.1:n.406-575C=
ENST00000553187.5:n.321-69C=
NM_001199771.1:c.311-69C=	NP_001186700.1:n.311-69C=
NM_002905.3:c.311-69C=	NP_002896.2:n.311-69C=
NR_037658.1:n.370-69C=
NM_001199771.2:c.311-69C=	NP_001186700.1:n.311-69C=
NM_002905.5:c.311-69C= MANE Select	NP_002896.2:n.311-69C=
NM_001199771.3:c.311-69C=	NP_001186700.1:n.311-69C=