Canonical Allele Identifier: CA385200896

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115610C>G (hg19) ; chr12:g.55721826C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721826C>G , CM000674.2:g.55721826C>G	GRCh38
NC_000012.11:g.56115610C>G , CM000674.1:g.56115610C>G	GRCh37
NC_000012.10:g.54401877C>G	NCBI36
NG_008606.1:g.6460C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000257895.10:c.448C>G MANE Select	ENSP00000257895.6:p.Leu150Val
ENST00000257895.9:c.448C>G	ENSP00000257895.5:p.Leu150Val
ENST00000257899.3:c.463C>G
ENST00000547072.5:c.157C>G	ENSP00000449927.1:p.Leu53Val
ENST00000547301.1:n.556C>G
ENST00000548082.1:c.448C>G	ENSP00000447128.1:p.Leu150Val
ENST00000548123.1:c.300+332C>G
ENST00000548486.1:n.458C>G
ENST00000550412.5:c.*120C>G	ENSP00000447650.1:n.*120C>G
ENST00000550608.1:n.587C>G
ENST00000551946.5:c.*251C>G	ENSP00000450201.1:n.*251C>G
ENST00000552930.5:c.157C>G	ENSP00000448014.1:p.Leu53Val
ENST00000553160.1:n.406-369C>G
ENST00000553187.5:n.458C>G
NM_001199771.1:c.448C>G	NP_001186700.1:p.Leu150Val
NM_002905.3:c.448C>G	NP_002896.2:p.Leu150Val
NR_037658.1:n.507C>G
NM_001199771.2:c.448C>G	NP_001186700.1:p.Leu150Val
NM_002905.5:c.448C>G MANE Select	NP_002896.2:p.Leu150Val
NM_001199771.3:c.448C>G	NP_001186700.1:p.Leu150Val