Canonical Allele Identifier: CA1924469958
Gene: RGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.84247517_84247524delinsCCACCCCA , CM000672.2:g.84247517_84247524delinsCCACCCCA GRCh38
NC_000010.10:g.86007273_86007280delinsCCACCCCA , CM000672.1:g.86007273_86007280delinsCCACCCCA GRCh37
NC_000010.9:g.85997253_85997260delinsCCACCCCA NCBI36
NG_009106.1:g.7465_7472delinsCCACCCCA

Transcript Alleles

HGVS Amino-acid change
ENST00000358110.7:c.80-74_80-67delinsCCACCCCA ENSP00000350823.5:n.80-74_80-67delinsCCACCCCA
ENST00000359452.9:c.80-74_80-67delinsCCACCCCA ENSP00000352427.4:n.80-74_80-67delinsCCACCCCA
ENST00000478727.6:c.*77_*84delinsCCACCCCA ENSP00000498966.1:n.*77_*84delinsCCACCCCA
ENST00000483744.6:c.80-74_80-67delinsCCACCCCA ENSP00000498992.1:n.80-74_80-67delinsCCACCCCA
ENST00000650682.1:c.-532_-525delinsCCACCCCA ENSP00000498223.1:n.-532_-525delinsCCACCCCA
ENST00000650774.1:c.80-124_80-117delinsCCACCCCA ENSP00000498908.1:n.80-124_80-117delinsCCACCCCA
ENST00000651155.1:c.80-74_80-67delinsCCACCCCA ENSP00000499193.1:n.80-74_80-67delinsCCACCCCA
ENST00000651237.1:c.-532_-525delinsCCACCCCA ENSP00000498404.1:n.-532_-525delinsCCACCCCA
ENST00000652073.1:c.-458-74_-458-67delinsCCACCCCA ENSP00000498800.1:n.-458-74_-458-67delinsCCACCCCA
ENST00000652092.2:c.80-74_80-67delinsCCACCCCA MANE Select ENSP00000498299.1:n.80-74_80-67delinsCCACCCCA
ENST00000652122.1:c.80-74_80-67delinsCCACCCCA ENSP00000498917.1:n.80-74_80-67delinsCCACCCCA
ENST00000652310.1:c.*58-124_*58-117delinsCCACCCCA ENSP00000498927.1:n.*58-124_*58-117delinsCCACCCCA
ENST00000358110.6:c.80-74_80-67delinsCCACCCCA ENSP00000350823.5:n.80-74_80-67delinsCCACCCCA
ENST00000359452.8:c.80-74_80-67delinsCCACCCCA ENSP00000352427.4:n.80-74_80-67delinsCCACCCCA
ENST00000372092.3:c.80-124_80-117delinsCCACCCCA ENSP00000361164.3:n.80-124_80-117delinsCCACCCCA
ENST00000469446.5:n.118-74_118-67delinsCCACCCCA
ENST00000478727.5:n.118-74_118-67delinsCCACCCCA
ENST00000483660.5:n.108-1405_108-1398delinsCCACCCCA
ENST00000483771.5:n.82-124_82-117delinsCCACCCCA
NM_001012720.1:c.80-74_80-67delinsCCACCCCA NP_001012738.1:n.80-74_80-67delinsCCACCCCA
NM_001012722.1:c.80-74_80-67delinsCCACCCCA NP_001012740.1:n.80-74_80-67delinsCCACCCCA
NM_002921.3:c.80-74_80-67delinsCCACCCCA NP_002912.2:n.80-74_80-67delinsCCACCCCA
XM_011540028.1:c.107-74_107-67delinsCCACCCCA XP_011538330.1:n.107-74_107-67delinsCCACCCCA
XM_024448118.1:c.80-74_80-67delinsCCACCCCA XP_024303886.1:n.80-74_80-67delinsCCACCCCA
XR_002957005.1:n.1430-74_1430-67delinsCCACCCCA
NM_001012720.2:c.80-74_80-67delinsCCACCCCA MANE Select NP_001012738.1:n.80-74_80-67delinsCCACCCCA
NM_001012722.2:c.80-74_80-67delinsCCACCCCA NP_001012740.1:n.80-74_80-67delinsCCACCCCA
NM_002921.4:c.80-74_80-67delinsCCACCCCA NP_002912.2:n.80-74_80-67delinsCCACCCCA