Canonical Allele Identifier: CA351714664
Gene: OGG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9756526A>C , CM000665.2:g.9756526A>C GRCh38
NC_000003.11:g.9798210A>C , CM000665.1:g.9798210A>C GRCh37
NC_000003.10:g.9773210A>C NCBI36
NG_012106.1:g.11583A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000302003.11:c.803A>C ENSP00000305584.7:p.Asp268Ala
ENST00000302008.12:c.803A>C ENSP00000305527.8:p.Asp268Ala
ENST00000302036.11:c.803A>C ENSP00000306561.7:p.Asp268Ala
ENST00000339511.9:c.803A>C ENSP00000345520.5:p.Asp268Ala
ENST00000344629.11:c.803A>C ENSP00000342851.7:p.Asp268Ala
ENST00000349503.9:c.747+1641A>C ENSP00000303132.6:p.=
ENST00000383826.9:c.565+4577A>C ENSP00000373337.5:p.=
ENST00000425665.1:c.*34A>C ENSP00000396034.1:p.=
ENST00000449570.6:c.803A>C ENSP00000403598.2:p.Asp268Ala
NM_002542.5:c.803A>C NP_002533.1:p.Asp268Ala
NM_016819.3:c.803A>C NP_058212.1:p.Asp268Ala
NM_016820.3:c.803A>C NP_058213.1:p.Asp268Ala
NM_016821.2:c.803A>C NP_058214.1:p.Asp268Ala
NM_016826.2:c.747+1641A>C NP_058434.1:p.=
NM_016827.2:c.565+4577A>C NP_058436.1:p.=
NM_016828.2:c.803A>C NP_058437.1:p.Asp268Ala
NM_016829.2:c.803A>C NP_058438.1:p.Asp268Ala
XM_011533760.1:c.803A>C XP_011532062.1:p.Asp268Ala
NM_001354648.1:c.566-241A>C NP_001341577.1:p.=
NM_001354649.1:c.566-241A>C NP_001341578.1:p.=
NM_001354650.1:c.748-241A>C NP_001341579.1:p.=
NM_001354651.1:c.803A>C NP_001341580.1:p.Asp268Ala
NM_001354652.1:c.748-241A>C NP_001341581.1:p.=
XM_011533760.2:c.803A>C XP_011532062.1:p.Asp268Ala
XM_017006493.2:c.748-241A>C XP_016861982.1:p.=
XM_017006494.2:c.748-241A>C XP_016861983.1:p.=
XM_017006495.2:c.748-241A>C XP_016861984.1:p.=
XM_017006496.2:c.803A>C XP_016861985.1:p.Asp268Ala
XM_017006497.2:c.748-241A>C XP_016861986.1:p.=
XM_017006499.2:c.748-241A>C XP_016861988.1:p.=
NM_001354648.2:c.566-241A>C NP_001341577.1:p.=
NM_001354649.2:c.566-241A>C NP_001341578.1:p.=
NM_001354650.2:c.748-241A>C NP_001341579.1:p.=
NM_001354651.2:c.803A>C NP_001341580.1:p.Asp268Ala
NM_001354652.2:c.748-241A>C NP_001341581.1:p.=
NM_002542.6:c.803A>C MANE Select NP_002533.1:p.Asp268Ala
NM_016819.4:c.803A>C NP_058212.1:p.Asp268Ala
NM_016820.4:c.803A>C NP_058213.1:p.Asp268Ala
NM_016821.3:c.803A>C NP_058214.1:p.Asp268Ala
NM_016826.3:c.747+1641A>C NP_058434.1:p.=
NM_016827.3:c.565+4577A>C NP_058436.1:p.=
NM_016828.3:c.803A>C NP_058437.1:p.Asp268Ala
NM_016829.3:c.803A>C NP_058438.1:p.Asp268Ala