Canonical Allele Identifier: CA377390889

Gene: RGR

Linked Data

• gnomAD v4: 10-84247717-C-T
• MyVariant Identifiers: chr10:g.86007473C>T (hg19) ; chr10:g.84247717C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.84247717C>T , CM000672.2:g.84247717C>T	GRCh38
NC_000010.10:g.86007473C>T , CM000672.1:g.86007473C>T	GRCh37
NC_000010.9:g.85997453C>T	NCBI36
NG_009106.1:g.7665C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358110.7:c.206C>T	ENSP00000350823.5:p.Ala69Val
ENST00000359452.9:c.206C>T	ENSP00000352427.4:p.Ala69Val
ENST00000478727.6:c.*277C>T	ENSP00000498966.1:n.*277C>T
ENST00000483744.6:c.206C>T	ENSP00000498992.1:p.Ala69Val
ENST00000650682.1:c.-332C>T	ENSP00000498223.1:n.-332C>T
ENST00000650774.1:c.156C>T	ENSP00000498908.1:p.Cys52=
ENST00000651155.1:c.206C>T	ENSP00000499193.1:p.Ala69Val
ENST00000651237.1:c.-332C>T	ENSP00000498404.1:n.-332C>T
ENST00000652073.1:c.-332C>T	ENSP00000498800.1:n.-332C>T
ENST00000652092.2:c.206C>T MANE Select	ENSP00000498299.1:p.Ala69Val
ENST00000652122.1:c.206C>T	ENSP00000498917.1:p.Ala69Val
ENST00000652310.1:c.*134C>T	ENSP00000498927.1:n.*134C>T
ENST00000358110.6:c.206C>T	ENSP00000350823.5:p.Ala69Val
ENST00000359452.8:c.206C>T	ENSP00000352427.4:p.Ala69Val
ENST00000372092.3:c.156C>T	ENSP00000361164.3:p.Cys52=
ENST00000469446.5:n.244C>T
ENST00000478727.5:n.244C>T
ENST00000483660.5:n.108-1205C>T
ENST00000483744.5:n.13C>T
ENST00000483771.5:n.158C>T
NM_001012720.1:c.206C>T	NP_001012738.1:p.Ala69Val
NM_001012722.1:c.206C>T	NP_001012740.1:p.Ala69Val
NM_002921.3:c.206C>T	NP_002912.2:p.Ala69Val
XM_011540028.1:c.233C>T	XP_011538330.1:p.Ala78Val
XM_024448118.1:c.206C>T	XP_024303886.1:p.Ala69Val
XR_002957005.1:n.1556C>T
NM_001012720.2:c.206C>T MANE Select	NP_001012738.1:p.Ala69Val
NM_001012722.2:c.206C>T	NP_001012740.1:p.Ala69Val
NM_002921.4:c.206C>T	NP_002912.2:p.Ala69Val