Canonical Allele Identifier: CA385201209

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115715T>A (hg19) ; chr12:g.55721931T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721931T>A , CM000674.2:g.55721931T>A	GRCh38
NC_000012.11:g.56115715T>A , CM000674.1:g.56115715T>A	GRCh37
NC_000012.10:g.54401982T>A	NCBI36
NG_008606.1:g.6565T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.553T>A MANE Select	ENSP00000257895.6:p.Phe185Ile
ENST00000257895.9:c.553T>A	ENSP00000257895.5:p.Phe185Ile
ENST00000257899.3:c.568T>A
ENST00000547072.5:c.262T>A	ENSP00000449927.1:p.Phe88Ile
ENST00000548082.1:c.553T>A	ENSP00000447128.1:p.Phe185Ile
ENST00000548123.1:c.300+437T>A
ENST00000548486.1:n.563T>A
ENST00000550412.5:c.*225T>A	ENSP00000447650.1:n.*225T>A
ENST00000550608.1:n.692T>A
ENST00000551946.5:c.*356T>A	ENSP00000450201.1:n.*356T>A
ENST00000553160.1:n.406-264T>A
ENST00000553187.5:n.563T>A
NM_001199771.1:c.553T>A	NP_001186700.1:p.Phe185Ile
NM_002905.3:c.553T>A	NP_002896.2:p.Phe185Ile
NR_037658.1:n.612T>A
NM_001199771.2:c.553T>A	NP_001186700.1:p.Phe185Ile
NM_002905.5:c.553T>A MANE Select	NP_002896.2:p.Phe185Ile
NM_001199771.3:c.553T>A	NP_001186700.1:p.Phe185Ile