Canonical Allele Identifier: CA351714388

Gene: OGG1

Linked Data

• MyVariant Identifiers: chr3:g.9798156T>A (hg19) ; chr3:g.9756472T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9756472T>A , CM000665.2:g.9756472T>A	GRCh38
NC_000003.11:g.9798156T>A , CM000665.1:g.9798156T>A	GRCh37
NC_000003.10:g.9773156T>A	NCBI36
NG_012106.1:g.11529T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302036.12:c.749T>A	ENSP00000306561.7:p.Val250Glu
ENST00000352937.6:c.747+1587T>A	ENSP00000344899.6:n.747+1587T>A
ENST00000707074.1:c.748-295T>A	ENSP00000516725.1:n.748-295T>A
ENST00000344629.12:c.749T>A MANE Select	ENSP00000342851.7:p.Val250Glu
ENST00000302003.11:c.749T>A	ENSP00000305584.7:p.Val250Glu
ENST00000302008.12:c.749T>A	ENSP00000305527.8:p.Val250Glu
ENST00000302036.11:c.749T>A	ENSP00000306561.7:p.Val250Glu
ENST00000339511.9:c.749T>A	ENSP00000345520.5:p.Val250Glu
ENST00000344629.11:c.749T>A	ENSP00000342851.7:p.Val250Glu
ENST00000349503.9:c.747+1587T>A	ENSP00000303132.6:n.747+1587T>A
ENST00000352937.5:c.463+1587T>A
ENST00000383825.2:n.48-295T>A
ENST00000383826.9:c.565+4523T>A	ENSP00000373337.5:n.565+4523T>A
ENST00000416333.1:c.49T>A
ENST00000425665.1:c.139T>A	ENSP00000396034.1:p.Trp47Arg
ENST00000426518.5:c.294+4523T>A
ENST00000429146.5:c.499T>A
ENST00000441094.5:c.442T>A
ENST00000449570.6:c.749T>A	ENSP00000403598.2:p.Val250Glu
NM_002542.5:c.749T>A	NP_002533.1:p.Val250Glu
NM_016819.3:c.749T>A	NP_058212.1:p.Val250Glu
NM_016820.3:c.749T>A	NP_058213.1:p.Val250Glu
NM_016821.2:c.749T>A	NP_058214.1:p.Val250Glu
NM_016826.2:c.747+1587T>A	NP_058434.1:n.747+1587T>A
NM_016827.2:c.565+4523T>A	NP_058436.1:n.565+4523T>A
NM_016828.2:c.749T>A	NP_058437.1:p.Val250Glu
NM_016829.2:c.749T>A	NP_058438.1:p.Val250Glu
XM_011533760.1:c.749T>A	XP_011532062.1:p.Val250Glu
NM_001354648.1:c.566-295T>A	NP_001341577.1:n.566-295T>A
NM_001354649.1:c.566-295T>A	NP_001341578.1:n.566-295T>A
NM_001354650.1:c.748-295T>A	NP_001341579.1:n.748-295T>A
NM_001354651.1:c.749T>A	NP_001341580.1:p.Val250Glu
NM_001354652.1:c.748-295T>A	NP_001341581.1:n.748-295T>A
NR_148930.1:n.844T>A
NR_148931.1:n.482T>A
NR_148932.1:n.910T>A
XM_011533760.2:c.749T>A	XP_011532062.1:p.Val250Glu
XM_017006493.2:c.748-295T>A	XP_016861982.1:n.748-295T>A
XM_017006494.2:c.748-295T>A	XP_016861983.1:n.748-295T>A
XM_017006495.2:c.748-295T>A	XP_016861984.1:n.748-295T>A
XM_017006496.2:c.749T>A	XP_016861985.1:p.Val250Glu
XM_017006497.2:c.748-295T>A	XP_016861986.1:n.748-295T>A
XM_017006499.2:c.748-295T>A	XP_016861988.1:n.748-295T>A
XR_001740156.2:n.1053T>A
NM_001354648.2:c.566-295T>A	NP_001341577.1:n.566-295T>A
NM_001354649.2:c.566-295T>A	NP_001341578.1:n.566-295T>A
NM_001354650.2:c.748-295T>A	NP_001341579.1:n.748-295T>A
NM_001354651.2:c.749T>A	NP_001341580.1:p.Val250Glu
NM_001354652.2:c.748-295T>A	NP_001341581.1:n.748-295T>A
NM_002542.6:c.749T>A MANE Select	NP_002533.1:p.Val250Glu
NM_016819.4:c.749T>A	NP_058212.1:p.Val250Glu
NM_016820.4:c.749T>A	NP_058213.1:p.Val250Glu
NM_016821.3:c.749T>A	NP_058214.1:p.Val250Glu
NM_016826.3:c.747+1587T>A	NP_058434.1:n.747+1587T>A
NM_016827.3:c.565+4523T>A	NP_058436.1:n.565+4523T>A
NM_016828.3:c.749T>A	NP_058437.1:p.Val250Glu
NM_016829.3:c.749T>A	NP_058438.1:p.Val250Glu
NR_148930.2:n.836T>A
NR_148931.2:n.474T>A
NR_148932.2:n.902T>A