Canonical Allele Identifier: CA1344887804
Gene: OGG1 HGNC NCBI

Linked Data

dbSNP Id: rs2077564694

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9756449del , CM000665.2:g.9756449del GRCh38
NC_000003.11:g.9798133del , CM000665.1:g.9798133del GRCh37
NC_000003.10:g.9773133del NCBI36
NG_012106.1:g.11506del

Transcript Alleles

HGVS Amino-acid Change
ENST00000302036.12:c.748-22del ENSP00000306561.7:n.748-22del
ENST00000352937.6:c.747+1564del ENSP00000344899.6:n.747+1564del
ENST00000707074.1:c.748-318del ENSP00000516725.1:n.748-318del
ENST00000344629.12:c.748-22del MANE Select ENSP00000342851.7:n.748-22del
ENST00000302003.11:c.748-22del ENSP00000305584.7:n.748-22del
ENST00000302008.12:c.748-22del ENSP00000305527.8:n.748-22del
ENST00000302036.11:c.748-22del ENSP00000306561.7:n.748-22del
ENST00000339511.9:c.748-22del ENSP00000345520.5:n.748-22del
ENST00000344629.11:c.748-22del ENSP00000342851.7:n.748-22del
ENST00000349503.9:c.747+1564del ENSP00000303132.6:n.747+1564del
ENST00000352937.5:c.463+1564del
ENST00000383825.2:n.48-318del
ENST00000383826.9:c.565+4500del ENSP00000373337.5:n.565+4500del
ENST00000416333.1:c.48-22del
ENST00000425665.1:c.138-22del ENSP00000396034.1:n.138-22del
ENST00000426518.5:c.294+4500del
ENST00000429146.5:c.498-22del
ENST00000441094.5:c.441-22del
ENST00000449570.6:c.748-22del ENSP00000403598.2:n.748-22del
NM_002542.5:c.748-22del NP_002533.1:n.748-22del
NM_016819.3:c.748-22del NP_058212.1:n.748-22del
NM_016820.3:c.748-22del NP_058213.1:n.748-22del
NM_016821.2:c.748-22del NP_058214.1:n.748-22del
NM_016826.2:c.747+1564del NP_058434.1:n.747+1564del
NM_016827.2:c.565+4500del NP_058436.1:n.565+4500del
NM_016828.2:c.748-22del NP_058437.1:n.748-22del
NM_016829.2:c.748-22del NP_058438.1:n.748-22del
XM_011533760.1:c.748-22del XP_011532062.1:n.748-22del
NM_001354648.1:c.566-318del NP_001341577.1:n.566-318del
NM_001354649.1:c.566-318del NP_001341578.1:n.566-318del
NM_001354650.1:c.748-318del NP_001341579.1:n.748-318del
NM_001354651.1:c.748-22del NP_001341580.1:n.748-22del
NM_001354652.1:c.748-318del NP_001341581.1:n.748-318del
NR_148930.1:n.843-22del
NR_148931.1:n.481-22del
NR_148932.1:n.909-22del
XM_011533760.2:c.748-22del XP_011532062.1:n.748-22del
XM_017006493.2:c.748-318del XP_016861982.1:n.748-318del
XM_017006494.2:c.748-318del XP_016861983.1:n.748-318del
XM_017006495.2:c.748-318del XP_016861984.1:n.748-318del
XM_017006496.2:c.748-22del XP_016861985.1:n.748-22del
XM_017006497.2:c.748-318del XP_016861986.1:n.748-318del
XM_017006499.2:c.748-318del XP_016861988.1:n.748-318del
XR_001740156.2:n.1052-22del
NM_001354648.2:c.566-318del NP_001341577.1:n.566-318del
NM_001354649.2:c.566-318del NP_001341578.1:n.566-318del
NM_001354650.2:c.748-318del NP_001341579.1:n.748-318del
NM_001354651.2:c.748-22del NP_001341580.1:n.748-22del
NM_001354652.2:c.748-318del NP_001341581.1:n.748-318del
NM_002542.6:c.748-22del MANE Select NP_002533.1:n.748-22del
NM_016819.4:c.748-22del NP_058212.1:n.748-22del
NM_016820.4:c.748-22del NP_058213.1:n.748-22del
NM_016821.3:c.748-22del NP_058214.1:n.748-22del
NM_016826.3:c.747+1564del NP_058434.1:n.747+1564del
NM_016827.3:c.565+4500del NP_058436.1:n.565+4500del
NM_016828.3:c.748-22del NP_058437.1:n.748-22del
NM_016829.3:c.748-22del NP_058438.1:n.748-22del
NR_148930.2:n.835-22del
NR_148931.2:n.473-22del
NR_148932.2:n.901-22del