Canonical Allele Identifier: CA385200909

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115616C>G (hg19) ; chr12:g.55721832C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721832C>G , CM000674.2:g.55721832C>G	GRCh38
NC_000012.11:g.56115616C>G , CM000674.1:g.56115616C>G	GRCh37
NC_000012.10:g.54401883C>G	NCBI36
NG_008606.1:g.6466C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.454C>G MANE Select	ENSP00000257895.6:p.Gln152Glu
ENST00000257895.9:c.454C>G	ENSP00000257895.5:p.Gln152Glu
ENST00000257899.3:c.469C>G
ENST00000547072.5:c.163C>G	ENSP00000449927.1:p.Gln55Glu
ENST00000548082.1:c.454C>G	ENSP00000447128.1:p.Gln152Glu
ENST00000548123.1:c.300+338C>G
ENST00000548486.1:n.464C>G
ENST00000550412.5:c.*126C>G	ENSP00000447650.1:n.*126C>G
ENST00000550608.1:n.593C>G
ENST00000551946.5:c.*257C>G	ENSP00000450201.1:n.*257C>G
ENST00000552930.5:c.163C>G	ENSP00000448014.1:p.Gln55Glu
ENST00000553160.1:n.406-363C>G
ENST00000553187.5:n.464C>G
NM_001199771.1:c.454C>G	NP_001186700.1:p.Gln152Glu
NM_002905.3:c.454C>G	NP_002896.2:p.Gln152Glu
NR_037658.1:n.513C>G
NM_001199771.2:c.454C>G	NP_001186700.1:p.Gln152Glu
NM_002905.5:c.454C>G MANE Select	NP_002896.2:p.Gln152Glu
NM_001199771.3:c.454C>G	NP_001186700.1:p.Gln152Glu