Canonical Allele Identifier: CA385201182

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115707T>A (hg19) ; chr12:g.55721923T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721923T>A , CM000674.2:g.55721923T>A	GRCh38
NC_000012.11:g.56115707T>A , CM000674.1:g.56115707T>A	GRCh37
NC_000012.10:g.54401974T>A	NCBI36
NG_008606.1:g.6557T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.545T>A MANE Select	ENSP00000257895.6:p.Leu182Gln
ENST00000257895.9:c.545T>A	ENSP00000257895.5:p.Leu182Gln
ENST00000257899.3:c.560T>A
ENST00000547072.5:c.254T>A	ENSP00000449927.1:p.Leu85Gln
ENST00000548082.1:c.545T>A	ENSP00000447128.1:p.Leu182Gln
ENST00000548123.1:c.300+429T>A
ENST00000548486.1:n.555T>A
ENST00000550412.5:c.*217T>A	ENSP00000447650.1:n.*217T>A
ENST00000550608.1:n.684T>A
ENST00000551946.5:c.*348T>A	ENSP00000450201.1:n.*348T>A
ENST00000553160.1:n.406-272T>A
ENST00000553187.5:n.555T>A
NM_001199771.1:c.545T>A	NP_001186700.1:p.Leu182Gln
NM_002905.3:c.545T>A	NP_002896.2:p.Leu182Gln
NR_037658.1:n.604T>A
NM_001199771.2:c.545T>A	NP_001186700.1:p.Leu182Gln
NM_002905.5:c.545T>A MANE Select	NP_002896.2:p.Leu182Gln
NM_001199771.3:c.545T>A	NP_001186700.1:p.Leu182Gln