Canonical Allele Identifier: CA11350223

Linked Data

dbSNP Id: rs293795
gnomAD v2: 3-9799113-A-G
gnomAD v3: 3-9757429-A-G
gnomAD v4: 3-9757429-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9757429A>G , CM000665.2:g.9757429A>G GRCh38
NC_000003.11:g.9799113A>G , CM000665.1:g.9799113A>G GRCh37
NC_000003.10:g.9774113A>G NCBI36
NG_012106.1:g.12486A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000302036.12:c.948+613A>G (OGG1) ENSP00000306561.7:n.948+613A>G
ENST00000352937.6:c.747+2544A>G (OGG1) ENSP00000344899.6:n.747+2544A>G
ENST00000707074.1:c.797+613A>G (OGG1) ENSP00000516725.1:n.797+613A>G
ENST00000256460.8:c.*110T>C (CAMK1) MANE Select ENSP00000256460.3:n.*110T>C
ENST00000256460.7:c.*110T>C (CAMK1) ENSP00000256460.3:n.*110T>C
ENST00000302008.12:c.948+613A>G (OGG1) ENSP00000305527.8:n.948+613A>G
ENST00000302036.11:c.948+613A>G (OGG1) ENSP00000306561.7:n.948+613A>G
ENST00000344629.11:c.*279A>G (OGG1) ENSP00000342851.7:n.*279A>G
ENST00000349503.9:c.747+2544A>G (OGG1) ENSP00000303132.6:n.747+2544A>G
ENST00000352937.5:c.463+2544A>G (OGG1)
ENST00000383826.9:c.565+5480A>G (OGG1) ENSP00000373337.5:n.565+5480A>G
ENST00000397277.6:c.*1104T>C (CAMK1) ENSP00000380447.2:n.*1104T>C
ENST00000421120.1:c.869T>C (CAMK1)
ENST00000426518.5:c.294+5480A>G (OGG1)
ENST00000449570.6:c.948+613A>G (OGG1) ENSP00000403598.2:n.948+613A>G
ENST00000482803.1:n.512T>C (CAMK1)
ENST00000496534.1:n.1405T>C (CAMK1)
ENST00000602976.1:n.82A>G (OGG1)
NM_003656.4:c.*110T>C (CAMK1) NP_003647.1:n.*110T>C
NM_016821.2:c.948+613A>G (OGG1) NP_058214.1:n.948+613A>G
NM_016826.2:c.747+2544A>G (OGG1) NP_058434.1:n.747+2544A>G
NM_016827.2:c.565+5480A>G (OGG1) NP_058436.1:n.565+5480A>G
NM_016828.2:c.948+613A>G (OGG1) NP_058437.1:n.948+613A>G
NM_016829.2:c.948+613A>G (OGG1) NP_058438.1:n.948+613A>G
XM_005265516.1:c.*88T>C (CAMK1) XP_005265573.1:n.*88T>C
XM_005265517.2:c.*88T>C (CAMK1) XP_005265574.1:n.*88T>C
XM_011533760.1:c.948+613A>G (OGG1) XP_011532062.1:n.948+613A>G
XR_940505.1:n.1249T>C (CAMK1)
NM_001354650.1:c.797+613A>G (OGG1) NP_001341579.1:n.797+613A>G
NM_001354651.1:c.898+808A>G (OGG1) NP_001341580.1:n.898+808A>G
NM_001354652.1:c.797+613A>G (OGG1) NP_001341581.1:n.797+613A>G
XM_005265516.2:c.*88T>C (CAMK1) XP_005265573.1:n.*88T>C
XM_005265517.3:c.*88T>C (CAMK1) XP_005265574.1:n.*88T>C
XM_011533760.2:c.948+613A>G (OGG1) XP_011532062.1:n.948+613A>G
XM_017006494.2:c.797+613A>G (OGG1) XP_016861983.1:n.797+613A>G
XM_017006496.2:c.948+613A>G (OGG1) XP_016861985.1:n.948+613A>G
XM_017006497.2:c.797+613A>G (OGG1) XP_016861986.1:n.797+613A>G
XM_017006499.2:c.797+613A>G (OGG1) XP_016861988.1:n.797+613A>G
XM_017007354.1:c.*110T>C (CAMK1) XP_016862843.1:n.*110T>C
XM_024453796.1:c.*110T>C (CAMK1) XP_024309564.1:n.*110T>C
XR_940505.2:n.1249T>C (CAMK1)
NM_003656.5:c.*110T>C (CAMK1) MANE Select NP_003647.1:n.*110T>C
NM_001354650.2:c.797+613A>G (OGG1) NP_001341579.1:n.797+613A>G
NM_001354651.2:c.898+808A>G (OGG1) NP_001341580.1:n.898+808A>G
NM_001354652.2:c.797+613A>G (OGG1) NP_001341581.1:n.797+613A>G
NM_016821.3:c.948+613A>G (OGG1) NP_058214.1:n.948+613A>G
NM_016826.3:c.747+2544A>G (OGG1) NP_058434.1:n.747+2544A>G
NM_016827.3:c.565+5480A>G (OGG1) NP_058436.1:n.565+5480A>G
NM_016828.3:c.948+613A>G (OGG1) NP_058437.1:n.948+613A>G
NM_016829.3:c.948+613A>G (OGG1) NP_058438.1:n.948+613A>G