Canonical Allele Identifier: CA1924469995

Gene: RGR

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.84247580_84247581delinsCT , CM000672.2:g.84247580_84247581delinsCT	GRCh38
NC_000010.10:g.86007336_86007337delinsCT , CM000672.1:g.86007336_86007337delinsCT	GRCh37
NC_000010.9:g.85997316_85997317delinsCT	NCBI36
NG_009106.1:g.7528_7529delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358110.7:c.80-11_80-10delinsCT	ENSP00000350823.5:n.80-11_80-10delinsCT
ENST00000359452.9:c.80-11_80-10delinsCT	ENSP00000352427.4:n.80-11_80-10delinsCT
ENST00000478727.6:c.*140_*141delinsCT	ENSP00000498966.1:n.*140_*141delinsCT
ENST00000483744.6:c.80-11_80-10delinsCT	ENSP00000498992.1:n.80-11_80-10delinsCT
ENST00000650682.1:c.-469_-468delinsCT	ENSP00000498223.1:n.-469_-468delinsCT
ENST00000650774.1:c.80-61_80-60delinsCT	ENSP00000498908.1:n.80-61_80-60delinsCT
ENST00000651155.1:c.80-11_80-10delinsCT	ENSP00000499193.1:n.80-11_80-10delinsCT
ENST00000651237.1:c.-469_-468delinsCT	ENSP00000498404.1:n.-469_-468delinsCT
ENST00000652073.1:c.-458-11_-458-10delinsCT	ENSP00000498800.1:n.-458-11_-458-10delinsCT
ENST00000652092.2:c.80-11_80-10delinsCT MANE Select	ENSP00000498299.1:n.80-11_80-10delinsCT
ENST00000652122.1:c.80-11_80-10delinsCT	ENSP00000498917.1:n.80-11_80-10delinsCT
ENST00000652310.1:c.*58-61_*58-60delinsCT	ENSP00000498927.1:n.*58-61_*58-60delinsCT
ENST00000358110.6:c.80-11_80-10delinsCT	ENSP00000350823.5:n.80-11_80-10delinsCT
ENST00000359452.8:c.80-11_80-10delinsCT	ENSP00000352427.4:n.80-11_80-10delinsCT
ENST00000372092.3:c.80-61_80-60delinsCT	ENSP00000361164.3:n.80-61_80-60delinsCT
ENST00000469446.5:n.118-11_118-10delinsCT
ENST00000478727.5:n.118-11_118-10delinsCT
ENST00000483660.5:n.108-1342_108-1341delinsCT
ENST00000483771.5:n.82-61_82-60delinsCT
NM_001012720.1:c.80-11_80-10delinsCT	NP_001012738.1:n.80-11_80-10delinsCT
NM_001012722.1:c.80-11_80-10delinsCT	NP_001012740.1:n.80-11_80-10delinsCT
NM_002921.3:c.80-11_80-10delinsCT	NP_002912.2:n.80-11_80-10delinsCT
XM_011540028.1:c.107-11_107-10delinsCT	XP_011538330.1:n.107-11_107-10delinsCT
XM_024448118.1:c.80-11_80-10delinsCT	XP_024303886.1:n.80-11_80-10delinsCT
XR_002957005.1:n.1430-11_1430-10delinsCT
NM_001012720.2:c.80-11_80-10delinsCT MANE Select	NP_001012738.1:n.80-11_80-10delinsCT
NM_001012722.2:c.80-11_80-10delinsCT	NP_001012740.1:n.80-11_80-10delinsCT
NM_002921.4:c.80-11_80-10delinsCT	NP_002912.2:n.80-11_80-10delinsCT