Canonical Allele Identifier: CA377390719

Gene: RGR

Linked Data

• MyVariant Identifiers: chr10:g.86007412A>C (hg19) ; chr10:g.84247656A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.84247656A>C , CM000672.2:g.84247656A>C	GRCh38
NC_000010.10:g.86007412A>C , CM000672.1:g.86007412A>C	GRCh37
NC_000010.9:g.85997392A>C	NCBI36
NG_009106.1:g.7604A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358110.7:c.145A>C	ENSP00000350823.5:p.Thr49Pro
ENST00000359452.9:c.145A>C	ENSP00000352427.4:p.Thr49Pro
ENST00000478727.6:c.*216A>C	ENSP00000498966.1:n.*216A>C
ENST00000483744.6:c.145A>C	ENSP00000498992.1:p.Thr49Pro
ENST00000650682.1:c.-393A>C	ENSP00000498223.1:n.-393A>C
ENST00000650774.1:c.95A>C	ENSP00000498908.1:p.Asp32Ala
ENST00000651155.1:c.145A>C	ENSP00000499193.1:p.Thr49Pro
ENST00000651237.1:c.-393A>C	ENSP00000498404.1:n.-393A>C
ENST00000652073.1:c.-393A>C	ENSP00000498800.1:n.-393A>C
ENST00000652092.2:c.145A>C MANE Select	ENSP00000498299.1:p.Thr49Pro
ENST00000652122.1:c.145A>C	ENSP00000498917.1:p.Thr49Pro
ENST00000652310.1:c.*73A>C	ENSP00000498927.1:n.*73A>C
ENST00000358110.6:c.145A>C	ENSP00000350823.5:p.Thr49Pro
ENST00000359452.8:c.145A>C	ENSP00000352427.4:p.Thr49Pro
ENST00000372092.3:c.95A>C	ENSP00000361164.3:p.Asp32Ala
ENST00000469446.5:n.183A>C
ENST00000478727.5:n.183A>C
ENST00000483660.5:n.108-1266A>C
ENST00000483771.5:n.97A>C
NM_001012720.1:c.145A>C	NP_001012738.1:p.Thr49Pro
NM_001012722.1:c.145A>C	NP_001012740.1:p.Thr49Pro
NM_002921.3:c.145A>C	NP_002912.2:p.Thr49Pro
XM_011540028.1:c.172A>C	XP_011538330.1:p.Thr58Pro
XM_024448118.1:c.145A>C	XP_024303886.1:p.Thr49Pro
XR_002957005.1:n.1495A>C
NM_001012720.2:c.145A>C MANE Select	NP_001012738.1:p.Thr49Pro
NM_001012722.2:c.145A>C	NP_001012740.1:p.Thr49Pro
NM_002921.4:c.145A>C	NP_002912.2:p.Thr49Pro