Canonical Allele Identifier: CA2038069337

Gene: RDH5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721533T= , CM000674.2:g.55721533T=	GRCh38
NC_000012.11:g.56115317T= , CM000674.1:g.56115317T=	GRCh37
NC_000012.10:g.54401584T=	NCBI36
NG_008606.1:g.6167T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.310+39T= MANE Select	ENSP00000257895.6:n.310+39T=
ENST00000257895.9:c.310+39T=	ENSP00000257895.5:n.310+39T=
ENST00000257899.3:c.326-156T=
ENST00000547072.5:c.19+39T=	ENSP00000449927.1:n.19+39T=
ENST00000547301.1:n.263T=
ENST00000548082.1:c.310+39T=	ENSP00000447128.1:n.310+39T=
ENST00000548123.1:c.300+39T=
ENST00000548486.1:n.320+39T=
ENST00000549424.1:c.118-156T=	ENSP00000447621.1:n.118-156T=
ENST00000550412.5:c.352-156T=	ENSP00000447650.1:n.352-156T=
ENST00000550608.1:n.449+39T=
ENST00000551946.5:c.*114-156T=	ENSP00000450201.1:n.*114-156T=
ENST00000552930.5:c.19+39T=	ENSP00000448014.1:n.19+39T=
ENST00000553160.1:n.406-662T=
ENST00000553187.5:n.320+39T=
NM_001199771.1:c.310+39T=	NP_001186700.1:n.310+39T=
NM_002905.3:c.310+39T=	NP_002896.2:n.310+39T=
NR_037658.1:n.370-156T=
NM_001199771.2:c.310+39T=	NP_001186700.1:n.310+39T=
NM_002905.5:c.310+39T= MANE Select	NP_002896.2:n.310+39T=
NM_001199771.3:c.310+39T=	NP_001186700.1:n.310+39T=