Canonical Allele Identifier: CA1924470091

Gene: RGR

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.84247778_84247779delinsTG , CM000672.2:g.84247778_84247779delinsTG	GRCh38
NC_000010.10:g.86007534_86007535delinsTG , CM000672.1:g.86007534_86007535delinsTG	GRCh37
NC_000010.9:g.85997514_85997515delinsTG	NCBI36
NG_009106.1:g.7726_7727delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358110.7:c.236+31_236+32delinsTG	ENSP00000350823.5:n.236+31_236+32delinsTG
ENST00000359452.9:c.236+31_236+32delinsTG	ENSP00000352427.4:n.236+31_236+32delinsTG
ENST00000478727.6:c.*307+31_*307+32delinsTG	ENSP00000498966.1:n.*307+31_*307+32delinsTG
ENST00000483744.6:c.236+31_236+32delinsTG	ENSP00000498992.1:n.236+31_236+32delinsTG
ENST00000650682.1:c.-302+31_-302+32delinsTG	ENSP00000498223.1:n.-302+31_-302+32delinsTG
ENST00000650774.1:c.186+31_186+32delinsTG	ENSP00000498908.1:n.186+31_186+32delinsTG
ENST00000651155.1:c.236+31_236+32delinsTG	ENSP00000499193.1:n.236+31_236+32delinsTG
ENST00000651237.1:c.-302+31_-302+32delinsTG	ENSP00000498404.1:n.-302+31_-302+32delinsTG
ENST00000652073.1:c.-302+31_-302+32delinsTG	ENSP00000498800.1:n.-302+31_-302+32delinsTG
ENST00000652092.2:c.236+31_236+32delinsTG MANE Select	ENSP00000498299.1:n.236+31_236+32delinsTG
ENST00000652122.1:c.236+31_236+32delinsTG	ENSP00000498917.1:n.236+31_236+32delinsTG
ENST00000652310.1:c.*164+31_*164+32delinsTG	ENSP00000498927.1:n.*164+31_*164+32delinsTG
ENST00000358110.6:c.236+31_236+32delinsTG	ENSP00000350823.5:n.236+31_236+32delinsTG
ENST00000359452.8:c.236+31_236+32delinsTG	ENSP00000352427.4:n.236+31_236+32delinsTG
ENST00000372092.3:c.186+31_186+32delinsTG	ENSP00000361164.3:n.186+31_186+32delinsTG
ENST00000469446.5:n.305_306delinsTG
ENST00000478727.5:n.274+31_274+32delinsTG
ENST00000483660.5:n.108-1144_108-1143delinsTG
ENST00000483744.5:n.43+31_43+32delinsTG
ENST00000483771.5:n.219_220delinsTG
NM_001012720.1:c.236+31_236+32delinsTG	NP_001012738.1:n.236+31_236+32delinsTG
NM_001012722.1:c.236+31_236+32delinsTG	NP_001012740.1:n.236+31_236+32delinsTG
NM_002921.3:c.236+31_236+32delinsTG	NP_002912.2:n.236+31_236+32delinsTG
XM_011540028.1:c.263+31_263+32delinsTG	XP_011538330.1:n.263+31_263+32delinsTG
XM_024448118.1:c.236+31_236+32delinsTG	XP_024303886.1:n.236+31_236+32delinsTG
XR_002957005.1:n.1586+31_1586+32delinsTG
NM_001012720.2:c.236+31_236+32delinsTG MANE Select	NP_001012738.1:n.236+31_236+32delinsTG
NM_001012722.2:c.236+31_236+32delinsTG	NP_001012740.1:n.236+31_236+32delinsTG
NM_002921.4:c.236+31_236+32delinsTG	NP_002912.2:n.236+31_236+32delinsTG