Canonical Allele Identifier: CA480155529

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115609T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721825T>A , CM000674.2:g.55721825T>A	GRCh38
NC_000012.11:g.56115609T>A , CM000674.1:g.56115609T>A	GRCh37
NC_000012.10:g.54401876T>A	NCBI36
NG_008606.1:g.6459T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.447T>A MANE Select	ENSP00000257895.6:p.Pro149=
ENST00000257895.9:c.447T>A	ENSP00000257895.5:p.Pro149=
ENST00000257899.3:c.462T>A
ENST00000547072.5:c.156T>A	ENSP00000449927.1:p.Pro52=
ENST00000547301.1:n.555T>A
ENST00000548082.1:c.447T>A	ENSP00000447128.1:p.Pro149=
ENST00000548123.1:c.300+331T>A
ENST00000548486.1:n.457T>A
ENST00000550412.5:c.*119T>A	ENSP00000447650.1:n.*119T>A
ENST00000550608.1:n.586T>A
ENST00000551946.5:c.*250T>A	ENSP00000450201.1:n.*250T>A
ENST00000552930.5:c.156T>A	ENSP00000448014.1:p.Pro52=
ENST00000553160.1:n.406-370T>A
ENST00000553187.5:n.457T>A
NM_001199771.1:c.447T>A	NP_001186700.1:p.Pro149=
NM_002905.3:c.447T>A	NP_002896.2:p.Pro149=
NR_037658.1:n.506T>A
NM_001199771.2:c.447T>A	NP_001186700.1:p.Pro149=
NM_002905.5:c.447T>A MANE Select	NP_002896.2:p.Pro149=
NM_001199771.3:c.447T>A	NP_001186700.1:p.Pro149=