Canonical Allele Identifier: CA2038069548

Gene: RDH5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721978C= , CM000674.2:g.55721978C=	GRCh38
NC_000012.11:g.56115762C= , CM000674.1:g.56115762C=	GRCh37
NC_000012.10:g.54402029C=	NCBI36
NG_008606.1:g.6612C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.569+31C= MANE Select	ENSP00000257895.6:n.569+31C=
ENST00000257895.9:c.569+31C=	ENSP00000257895.5:n.569+31C=
ENST00000257899.3:c.591+24C=
ENST00000547072.5:c.278+31C=	ENSP00000449927.1:n.278+31C=
ENST00000548082.1:c.569+31C=	ENSP00000447128.1:n.569+31C=
ENST00000548123.1:c.300+484C=
ENST00000548486.1:n.610C=
ENST00000550412.5:c.*272C=	ENSP00000447650.1:n.*272C=
ENST00000550608.1:n.739C=
ENST00000551946.5:c.*403C=	ENSP00000450201.1:n.*403C=
ENST00000553160.1:n.406-217C=
ENST00000553187.5:n.610C=
NM_001199771.1:c.569+31C=	NP_001186700.1:n.569+31C=
NM_002905.3:c.569+31C=	NP_002896.2:n.569+31C=
NR_037658.1:n.628+31C=
NM_001199771.2:c.569+31C=	NP_001186700.1:n.569+31C=
NM_002905.5:c.569+31C= MANE Select	NP_002896.2:n.569+31C=
NM_001199771.3:c.569+31C=	NP_001186700.1:n.569+31C=