Canonical Allele Identifier: CA385201262

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115730A>G (hg19) ; chr12:g.55721946A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721946A>G , CM000674.2:g.55721946A>G	GRCh38
NC_000012.11:g.56115730A>G , CM000674.1:g.56115730A>G	GRCh37
NC_000012.10:g.54401997A>G	NCBI36
NG_008606.1:g.6580A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.568A>G MANE Select	ENSP00000257895.6:p.Arg190Gly
ENST00000257895.9:c.568A>G	ENSP00000257895.5:p.Arg190Gly
ENST00000257899.3:c.583A>G
ENST00000547072.5:c.277A>G	ENSP00000449927.1:p.Arg93Gly
ENST00000548082.1:c.568A>G	ENSP00000447128.1:p.Arg190Gly
ENST00000548123.1:c.300+452A>G
ENST00000548486.1:n.578A>G
ENST00000550412.5:c.*240A>G	ENSP00000447650.1:n.*240A>G
ENST00000550608.1:n.707A>G
ENST00000551946.5:c.*371A>G	ENSP00000450201.1:n.*371A>G
ENST00000553160.1:n.406-249A>G
ENST00000553187.5:n.578A>G
NM_001199771.1:c.568A>G	NP_001186700.1:p.Arg190Gly
NM_002905.3:c.568A>G	NP_002896.2:p.Arg190Gly
NR_037658.1:n.627A>G
NM_001199771.2:c.568A>G	NP_001186700.1:p.Arg190Gly
NM_002905.5:c.568A>G MANE Select	NP_002896.2:p.Arg190Gly
NM_001199771.3:c.568A>G	NP_001186700.1:p.Arg190Gly