Canonical Allele Identifier: CA2038069569

Gene: RDH5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55722052A= , CM000674.2:g.55722052A=	GRCh38
NC_000012.11:g.56115836A= , CM000674.1:g.56115836A=	GRCh37
NC_000012.10:g.54402103A=	NCBI36
NG_008606.1:g.6686A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.569+105A= MANE Select	ENSP00000257895.6:n.569+105A=
ENST00000257895.9:c.569+105A=	ENSP00000257895.5:n.569+105A=
ENST00000257899.3:c.591+98A=
ENST00000547072.5:c.278+105A=	ENSP00000449927.1:n.278+105A=
ENST00000548082.1:c.569+105A=	ENSP00000447128.1:n.569+105A=
ENST00000548123.1:c.300+558A=
ENST00000548486.1:n.684A=
ENST00000550412.5:c.*346A=	ENSP00000447650.1:n.*346A=
ENST00000550608.1:n.813A=
ENST00000551946.5:c.*477A=	ENSP00000450201.1:n.*477A=
ENST00000553160.1:n.406-143A=
NM_001199771.1:c.569+105A=	NP_001186700.1:n.569+105A=
NM_002905.3:c.569+105A=	NP_002896.2:n.569+105A=
NR_037658.1:n.628+105A=
NM_001199771.2:c.569+105A=	NP_001186700.1:n.569+105A=
NM_002905.5:c.569+105A= MANE Select	NP_002896.2:n.569+105A=
NM_001199771.3:c.569+105A=	NP_001186700.1:n.569+105A=