Canonical Allele Identifier: CA351709777

Gene: OGG1

Linked Data

• MyVariant Identifiers: chr3:g.9792649C>T (hg19) ; chr3:g.9750965C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9750965C>T , CM000665.2:g.9750965C>T	GRCh38
NC_000003.11:g.9792649C>T , CM000665.1:g.9792649C>T	GRCh37
NC_000003.10:g.9767649C>T	NCBI36
NG_012106.1:g.6022C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302036.12:c.158C>T	ENSP00000306561.7:p.Ala53Val
ENST00000352937.6:c.158C>T	ENSP00000344899.6:p.Ala53Val
ENST00000707074.1:c.158C>T	ENSP00000516725.1:p.Ala53Val
ENST00000344629.12:c.158C>T MANE Select	ENSP00000342851.7:p.Ala53Val
ENST00000302003.11:c.158C>T	ENSP00000305584.7:p.Ala53Val
ENST00000302008.12:c.158C>T	ENSP00000305527.8:p.Ala53Val
ENST00000302036.11:c.158C>T	ENSP00000306561.7:p.Ala53Val
ENST00000339511.9:c.158C>T	ENSP00000345520.5:p.Ala53Val
ENST00000344629.11:c.158C>T	ENSP00000342851.7:p.Ala53Val
ENST00000349503.9:c.158C>T	ENSP00000303132.6:p.Ala53Val
ENST00000383826.9:c.158C>T	ENSP00000373337.5:p.Ala53Val
ENST00000425665.1:c.137+542C>T	ENSP00000396034.1:n.137+542C>T
ENST00000429146.5:c.90C>T
ENST00000432857.2:n.2C>T
ENST00000436092.1:n.707C>T
ENST00000441094.5:c.78+542C>T
ENST00000449570.6:c.158C>T	ENSP00000403598.2:p.Ala53Val
NM_002542.5:c.158C>T	NP_002533.1:p.Ala53Val
NM_016819.3:c.158C>T	NP_058212.1:p.Ala53Val
NM_016820.3:c.158C>T	NP_058213.1:p.Ala53Val
NM_016821.2:c.158C>T	NP_058214.1:p.Ala53Val
NM_016826.2:c.158C>T	NP_058434.1:p.Ala53Val
NM_016827.2:c.158C>T	NP_058436.1:p.Ala53Val
NM_016828.2:c.158C>T	NP_058437.1:p.Ala53Val
NM_016829.2:c.158C>T	NP_058438.1:p.Ala53Val
XM_011533760.1:c.158C>T	XP_011532062.1:p.Ala53Val
XM_011533761.1:c.158C>T	XP_011532063.1:p.Ala53Val
NM_001354648.1:c.158C>T	NP_001341577.1:p.Ala53Val
NM_001354649.1:c.158C>T	NP_001341578.1:p.Ala53Val
NM_001354650.1:c.158C>T	NP_001341579.1:p.Ala53Val
NM_001354651.1:c.158C>T	NP_001341580.1:p.Ala53Val
NM_001354652.1:c.158C>T	NP_001341581.1:p.Ala53Val
NR_148930.1:n.480+542C>T
NR_148931.1:n.480+542C>T
NR_148932.1:n.501C>T
XM_011533760.2:c.158C>T	XP_011532062.1:p.Ala53Val
XM_017006493.2:c.158C>T	XP_016861982.1:p.Ala53Val
XM_017006494.2:c.158C>T	XP_016861983.1:p.Ala53Val
XM_017006495.2:c.158C>T	XP_016861984.1:p.Ala53Val
XM_017006496.2:c.158C>T	XP_016861985.1:p.Ala53Val
XM_017006497.2:c.158C>T	XP_016861986.1:p.Ala53Val
XM_017006499.2:c.158C>T	XP_016861988.1:p.Ala53Val
XR_001740156.2:n.454C>T
NM_001354648.2:c.158C>T	NP_001341577.1:p.Ala53Val
NM_001354649.2:c.158C>T	NP_001341578.1:p.Ala53Val
NM_001354650.2:c.158C>T	NP_001341579.1:p.Ala53Val
NM_001354651.2:c.158C>T	NP_001341580.1:p.Ala53Val
NM_001354652.2:c.158C>T	NP_001341581.1:p.Ala53Val
NM_002542.6:c.158C>T MANE Select	NP_002533.1:p.Ala53Val
NM_016819.4:c.158C>T	NP_058212.1:p.Ala53Val
NM_016820.4:c.158C>T	NP_058213.1:p.Ala53Val
NM_016821.3:c.158C>T	NP_058214.1:p.Ala53Val
NM_016826.3:c.158C>T	NP_058434.1:p.Ala53Val
NM_016827.3:c.158C>T	NP_058436.1:p.Ala53Val
NM_016828.3:c.158C>T	NP_058437.1:p.Ala53Val
NM_016829.3:c.158C>T	NP_058438.1:p.Ala53Val
NR_148930.2:n.472+542C>T
NR_148931.2:n.472+542C>T
NR_148932.2:n.493C>T