Canonical Allele Identifier: CA1344888117
Gene: OGG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9757089C= , CM000665.2:g.9757089C= GRCh38
NC_000003.11:g.9798773C= , CM000665.1:g.9798773C= GRCh37
NC_000003.10:g.9773773C= NCBI36
NG_012106.1:g.12146C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302036.12:c.948+273C= ENSP00000306561.7:n.948+273C=
ENST00000352937.6:c.747+2204C= ENSP00000344899.6:n.747+2204C=
ENST00000707074.1:c.797+273C= ENSP00000516725.1:n.797+273C=
ENST00000344629.12:c.977C= MANE Select ENSP00000342851.7:p.Ser326=
ENST00000302003.11:c.994C= ENSP00000305584.7:p.Pro332=
ENST00000302008.12:c.948+273C= ENSP00000305527.8:n.948+273C=
ENST00000302036.11:c.948+273C= ENSP00000306561.7:n.948+273C=
ENST00000339511.9:c.*246C= ENSP00000345520.5:n.*246C=
ENST00000344629.11:c.977C= ENSP00000342851.7:p.Ser326=
ENST00000349503.9:c.747+2204C= ENSP00000303132.6:n.747+2204C=
ENST00000352937.5:c.463+2204C=
ENST00000383825.2:n.370C=
ENST00000383826.9:c.565+5140C= ENSP00000373337.5:n.565+5140C=
ENST00000416333.1:c.294C=
ENST00000425665.1:c.*452C= ENSP00000396034.1:n.*452C=
ENST00000426518.5:c.294+5140C=
ENST00000449570.6:c.948+273C= ENSP00000403598.2:n.948+273C=
NM_002542.5:c.977C= NP_002533.1:p.Ser326=
NM_016819.3:c.*246C= NP_058212.1:n.*246C=
NM_016820.3:c.994C= NP_058213.1:p.Pro332=
NM_016821.2:c.948+273C= NP_058214.1:n.948+273C=
NM_016826.2:c.747+2204C= NP_058434.1:n.747+2204C=
NM_016827.2:c.565+5140C= NP_058436.1:n.565+5140C=
NM_016828.2:c.948+273C= NP_058437.1:n.948+273C=
NM_016829.2:c.948+273C= NP_058438.1:n.948+273C=
XM_011533760.1:c.948+273C= XP_011532062.1:n.948+273C=
NM_001354648.1:c.*246C= NP_001341577.1:n.*246C=
NM_001354649.1:c.644C= NP_001341578.1:p.Ser215=
NM_001354650.1:c.797+273C= NP_001341579.1:n.797+273C=
NM_001354651.1:c.898+468C= NP_001341580.1:n.898+468C=
NM_001354652.1:c.797+273C= NP_001341581.1:n.797+273C=
NR_148930.1:n.1316C=
NR_148931.1:n.954C=
NR_148932.1:n.1382C=
XM_011533760.2:c.948+273C= XP_011532062.1:n.948+273C=
XM_017006493.2:c.826C= XP_016861982.1:p.Pro276=
XM_017006494.2:c.797+273C= XP_016861983.1:n.797+273C=
XM_017006495.2:c.843C= XP_016861984.1:p.Ile281=
XM_017006496.2:c.948+273C= XP_016861985.1:n.948+273C=
XM_017006497.2:c.797+273C= XP_016861986.1:n.797+273C=
XM_017006499.2:c.797+273C= XP_016861988.1:n.797+273C=
NM_001354648.2:c.*246C= NP_001341577.1:n.*246C=
NM_001354649.2:c.644C= NP_001341578.1:p.Ser215=
NM_001354650.2:c.797+273C= NP_001341579.1:n.797+273C=
NM_001354651.2:c.898+468C= NP_001341580.1:n.898+468C=
NM_001354652.2:c.797+273C= NP_001341581.1:n.797+273C=
NM_002542.6:c.977C= MANE Select NP_002533.1:p.Ser326=
NM_016819.4:c.*246C= NP_058212.1:n.*246C=
NM_016820.4:c.994C= NP_058213.1:p.Pro332=
NM_016821.3:c.948+273C= NP_058214.1:n.948+273C=
NM_016826.3:c.747+2204C= NP_058434.1:n.747+2204C=
NM_016827.3:c.565+5140C= NP_058436.1:n.565+5140C=
NM_016828.3:c.948+273C= NP_058437.1:n.948+273C=
NM_016829.3:c.948+273C= NP_058438.1:n.948+273C=
NR_148930.2:n.1308C=
NR_148931.2:n.946C=
NR_148932.2:n.1374C=