Canonical Allele Identifier: CA1924470018
Gene: RGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.84247623_84247626delinsATCT , CM000672.2:g.84247623_84247626delinsATCT GRCh38
NC_000010.10:g.86007379_86007382delinsATCT , CM000672.1:g.86007379_86007382delinsATCT GRCh37
NC_000010.9:g.85997359_85997362delinsATCT NCBI36
NG_009106.1:g.7571_7574delinsATCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000358110.7:c.112_115delinsATCT ENSP00000350823.5:p.Ile38=
ENST00000359452.9:c.112_115delinsATCT ENSP00000352427.4:p.Ile38=
ENST00000478727.6:c.*183_*186delinsATCT ENSP00000498966.1:n.*183_*186delinsATCT
ENST00000483744.6:c.112_115delinsATCT ENSP00000498992.1:p.Ile38=
ENST00000650682.1:c.-426_-423delinsATCT ENSP00000498223.1:n.-426_-423delinsATCT
ENST00000650774.1:c.80-18_80-15delinsATCT ENSP00000498908.1:n.80-18_80-15delinsATCT
ENST00000651155.1:c.112_115delinsATCT ENSP00000499193.1:p.Ile38=
ENST00000651237.1:c.-426_-423delinsATCT ENSP00000498404.1:n.-426_-423delinsATCT
ENST00000652073.1:c.-426_-423delinsATCT ENSP00000498800.1:n.-426_-423delinsATCT
ENST00000652092.2:c.112_115delinsATCT MANE Select ENSP00000498299.1:p.Ile38=
ENST00000652122.1:c.112_115delinsATCT ENSP00000498917.1:p.Ile38=
ENST00000652310.1:c.*58-18_*58-15delinsATCT ENSP00000498927.1:n.*58-18_*58-15delinsATCT
ENST00000358110.6:c.112_115delinsATCT ENSP00000350823.5:p.Ile38=
ENST00000359452.8:c.112_115delinsATCT ENSP00000352427.4:p.Ile38=
ENST00000372092.3:c.80-18_80-15delinsATCT ENSP00000361164.3:n.80-18_80-15delinsATCT
ENST00000469446.5:n.150_153delinsATCT
ENST00000478727.5:n.150_153delinsATCT
ENST00000483660.5:n.108-1299_108-1296delinsATCT
ENST00000483771.5:n.82-18_82-15delinsATCT
NM_001012720.1:c.112_115delinsATCT NP_001012738.1:p.Ile38=
NM_001012722.1:c.112_115delinsATCT NP_001012740.1:p.Ile38=
NM_002921.3:c.112_115delinsATCT NP_002912.2:p.Ile38=
XM_011540028.1:c.139_142delinsATCT XP_011538330.1:p.Ile47=
XM_024448118.1:c.112_115delinsATCT XP_024303886.1:p.Ile38=
XR_002957005.1:n.1462_1465delinsATCT
NM_001012720.2:c.112_115delinsATCT MANE Select NP_001012738.1:p.Ile38=
NM_001012722.2:c.112_115delinsATCT NP_001012740.1:p.Ile38=
NM_002921.4:c.112_115delinsATCT NP_002912.2:p.Ile38=