Canonical Allele Identifier: CA377390641

Gene: RGR

Linked Data

• MyVariant Identifiers: chr10:g.86007381C>G (hg19) ; chr10:g.84247625C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.84247625C>G , CM000672.2:g.84247625C>G	GRCh38
NC_000010.10:g.86007381C>G , CM000672.1:g.86007381C>G	GRCh37
NC_000010.9:g.85997361C>G	NCBI36
NG_009106.1:g.7573C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358110.7:c.114C>G	ENSP00000350823.5:p.Ile38Met
ENST00000359452.9:c.114C>G	ENSP00000352427.4:p.Ile38Met
ENST00000478727.6:c.*185C>G	ENSP00000498966.1:n.*185C>G
ENST00000483744.6:c.114C>G	ENSP00000498992.1:p.Ile38Met
ENST00000650682.1:c.-424C>G	ENSP00000498223.1:n.-424C>G
ENST00000650774.1:c.80-16C>G	ENSP00000498908.1:n.80-16C>G
ENST00000651155.1:c.114C>G	ENSP00000499193.1:p.Ile38Met
ENST00000651237.1:c.-424C>G	ENSP00000498404.1:n.-424C>G
ENST00000652073.1:c.-424C>G	ENSP00000498800.1:n.-424C>G
ENST00000652092.2:c.114C>G MANE Select	ENSP00000498299.1:p.Ile38Met
ENST00000652122.1:c.114C>G	ENSP00000498917.1:p.Ile38Met
ENST00000652310.1:c.*58-16C>G	ENSP00000498927.1:n.*58-16C>G
ENST00000358110.6:c.114C>G	ENSP00000350823.5:p.Ile38Met
ENST00000359452.8:c.114C>G	ENSP00000352427.4:p.Ile38Met
ENST00000372092.3:c.80-16C>G	ENSP00000361164.3:n.80-16C>G
ENST00000469446.5:n.152C>G
ENST00000478727.5:n.152C>G
ENST00000483660.5:n.108-1297C>G
ENST00000483771.5:n.82-16C>G
NM_001012720.1:c.114C>G	NP_001012738.1:p.Ile38Met
NM_001012722.1:c.114C>G	NP_001012740.1:p.Ile38Met
NM_002921.3:c.114C>G	NP_002912.2:p.Ile38Met
XM_011540028.1:c.141C>G	XP_011538330.1:p.Ile47Met
XM_024448118.1:c.114C>G	XP_024303886.1:p.Ile38Met
XR_002957005.1:n.1464C>G
NM_001012720.2:c.114C>G MANE Select	NP_001012738.1:p.Ile38Met
NM_001012722.2:c.114C>G	NP_001012740.1:p.Ile38Met
NM_002921.4:c.114C>G	NP_002912.2:p.Ile38Met