Canonical Allele Identifier: CA377390903

Gene: RGR

Linked Data

• ClinVar Variation Id: 2856461
• ClinVar RCV Id: RCV003696461
• MyVariant Identifiers: chr10:g.86007479T>G (hg19) ; chr10:g.84247723T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.84247723T>G , CM000672.2:g.84247723T>G	GRCh38
NC_000010.10:g.86007479T>G , CM000672.1:g.86007479T>G	GRCh37
NC_000010.9:g.85997459T>G	NCBI36
NG_009106.1:g.7671T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358110.7:c.212T>G	ENSP00000350823.5:p.Val71Gly
ENST00000359452.9:c.212T>G	ENSP00000352427.4:p.Val71Gly
ENST00000478727.6:c.*283T>G	ENSP00000498966.1:n.*283T>G
ENST00000483744.6:c.212T>G	ENSP00000498992.1:p.Val71Gly
ENST00000650682.1:c.-326T>G	ENSP00000498223.1:n.-326T>G
ENST00000650774.1:c.162T>G	ENSP00000498908.1:p.Arg54=
ENST00000651155.1:c.212T>G	ENSP00000499193.1:p.Val71Gly
ENST00000651237.1:c.-326T>G	ENSP00000498404.1:n.-326T>G
ENST00000652073.1:c.-326T>G	ENSP00000498800.1:n.-326T>G
ENST00000652092.2:c.212T>G MANE Select	ENSP00000498299.1:p.Val71Gly
ENST00000652122.1:c.212T>G	ENSP00000498917.1:p.Val71Gly
ENST00000652310.1:c.*140T>G	ENSP00000498927.1:n.*140T>G
ENST00000358110.6:c.212T>G	ENSP00000350823.5:p.Val71Gly
ENST00000359452.8:c.212T>G	ENSP00000352427.4:p.Val71Gly
ENST00000372092.3:c.162T>G	ENSP00000361164.3:p.Arg54=
ENST00000469446.5:n.250T>G
ENST00000478727.5:n.250T>G
ENST00000483660.5:n.108-1199T>G
ENST00000483744.5:n.19T>G
ENST00000483771.5:n.164T>G
NM_001012720.1:c.212T>G	NP_001012738.1:p.Val71Gly
NM_001012722.1:c.212T>G	NP_001012740.1:p.Val71Gly
NM_002921.3:c.212T>G	NP_002912.2:p.Val71Gly
XM_011540028.1:c.239T>G	XP_011538330.1:p.Val80Gly
XM_024448118.1:c.212T>G	XP_024303886.1:p.Val71Gly
XR_002957005.1:n.1562T>G
NM_001012720.2:c.212T>G MANE Select	NP_001012738.1:p.Val71Gly
NM_001012722.2:c.212T>G	NP_001012740.1:p.Val71Gly
NM_002921.4:c.212T>G	NP_002912.2:p.Val71Gly