Canonical Allele Identifier: CA1924470121

Gene: RGR

Linked Data

• dbSNP Id: rs1842766981

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.84247824_84247825insCTGGGCAGCCAGACC , CM000672.2:g.84247824_84247825insCTGGGCAGCCAGACC	GRCh38
NC_000010.10:g.86007580_86007581insCTGGGCAGCCAGACC , CM000672.1:g.86007580_86007581insCTGGGCAGCCAGACC	GRCh37
NC_000010.9:g.85997560_85997561insCTGGGCAGCCAGACC	NCBI36
NG_009106.1:g.7772_7773insCTGGGCAGCCAGACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358110.7:c.236+77_236+78insCTGGGCAGCCAGACC	ENSP00000350823.5:n.236+77_236+78insCTGGGCAGCCAGACC
ENST00000359452.9:c.236+77_236+78insCTGGGCAGCCAGACC	ENSP00000352427.4:n.236+77_236+78insCTGGGCAGCCAGACC
ENST00000478727.6:c.*307+77_*307+78insCTGGGCAGCCAGACC	ENSP00000498966.1:n.*307+77_*307+78insCTGGGCAGCCAGACC
ENST00000483744.6:c.236+77_236+78insCTGGGCAGCCAGACC	ENSP00000498992.1:n.236+77_236+78insCTGGGCAGCCAGACC
ENST00000650682.1:c.-302+77_-302+78insCTGGGCAGCCAGACC	ENSP00000498223.1:n.-302+77_-302+78insCTGGGCAGCCAGACC
ENST00000650774.1:c.186+77_186+78insCTGGGCAGCCAGACC	ENSP00000498908.1:n.186+77_186+78insCTGGGCAGCCAGACC
ENST00000651155.1:c.236+77_236+78insCTGGGCAGCCAGACC	ENSP00000499193.1:n.236+77_236+78insCTGGGCAGCCAGACC
ENST00000651237.1:c.-302+77_-302+78insCTGGGCAGCCAGACC	ENSP00000498404.1:n.-302+77_-302+78insCTGGGCAGCCAGACC
ENST00000652073.1:c.-302+77_-302+78insCTGGGCAGCCAGACC	ENSP00000498800.1:n.-302+77_-302+78insCTGGGCAGCCAGACC
ENST00000652092.2:c.236+77_236+78insCTGGGCAGCCAGACC MANE Select	ENSP00000498299.1:n.236+77_236+78insCTGGGCAGCCAGACC
ENST00000652122.1:c.236+77_236+78insCTGGGCAGCCAGACC	ENSP00000498917.1:n.236+77_236+78insCTGGGCAGCCAGACC
ENST00000652310.1:c.*164+77_*164+78insCTGGGCAGCCAGACC	ENSP00000498927.1:n.*164+77_*164+78insCTGGGCAGCCAGACC
ENST00000358110.6:c.236+77_236+78insCTGGGCAGCCAGACC	ENSP00000350823.5:n.236+77_236+78insCTGGGCAGCCAGACC
ENST00000359452.8:c.236+77_236+78insCTGGGCAGCCAGACC	ENSP00000352427.4:n.236+77_236+78insCTGGGCAGCCAGACC
ENST00000372092.3:c.186+77_186+78insCTGGGCAGCCAGACC	ENSP00000361164.3:n.186+77_186+78insCTGGGCAGCCAGACC
ENST00000469446.5:n.351_352insCTGGGCAGCCAGACC
ENST00000478727.5:n.274+77_274+78insCTGGGCAGCCAGACC
ENST00000483660.5:n.108-1098_108-1097insCTGGGCAGCCAGACC
ENST00000483744.5:n.43+77_43+78insCTGGGCAGCCAGACC
ENST00000483771.5:n.265_266insCTGGGCAGCCAGACC
NM_001012720.1:c.236+77_236+78insCTGGGCAGCCAGACC	NP_001012738.1:n.236+77_236+78insCTGGGCAGCCAGACC
NM_001012722.1:c.236+77_236+78insCTGGGCAGCCAGACC	NP_001012740.1:n.236+77_236+78insCTGGGCAGCCAGACC
NM_002921.3:c.236+77_236+78insCTGGGCAGCCAGACC	NP_002912.2:n.236+77_236+78insCTGGGCAGCCAGACC
XM_011540028.1:c.263+77_263+78insCTGGGCAGCCAGACC	XP_011538330.1:n.263+77_263+78insCTGGGCAGCCAGACC
XM_024448118.1:c.236+77_236+78insCTGGGCAGCCAGACC	XP_024303886.1:n.236+77_236+78insCTGGGCAGCCAGACC
XR_002957005.1:n.1586+77_1586+78insCTGGGCAGCCAGACC
NM_001012720.2:c.236+77_236+78insCTGGGCAGCCAGACC MANE Select	NP_001012738.1:n.236+77_236+78insCTGGGCAGCCAGACC
NM_001012722.2:c.236+77_236+78insCTGGGCAGCCAGACC	NP_001012740.1:n.236+77_236+78insCTGGGCAGCCAGACC
NM_002921.4:c.236+77_236+78insCTGGGCAGCCAGACC	NP_002912.2:n.236+77_236+78insCTGGGCAGCCAGACC