Canonical Allele Identifier: CA15228127

Gene: OGG1 CAMK1

Linked Data

• dbSNP Id: rs2304277
• gnomAD v2: 3-9801080-G-A
• gnomAD v3: 3-9759396-G-A
• gnomAD v4: 3-9759396-G-A
• MyVariant Identifiers: chr3:g.9801080G>A (hg19) ; chr3:g.9759396G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9759396G>A , CM000665.2:g.9759396G>A	GRCh38
NC_000003.11:g.9801080G>A , CM000665.1:g.9801080G>A	GRCh37
NC_000003.10:g.9776080G>A	NCBI36
NG_012106.1:g.14453G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302036.12:c.948+2580G>A (OGG1)	ENSP00000306561.7:n.948+2580G>A
ENST00000352937.6:c.747+4511G>A (OGG1)	ENSP00000344899.6:n.747+4511G>A
ENST00000707074.1:c.797+2580G>A (OGG1)	ENSP00000516725.1:n.797+2580G>A
ENST00000256460.8:c.912+92C>T (CAMK1) MANE Select	ENSP00000256460.3:n.912+92C>T
ENST00000256460.7:c.912+92C>T (CAMK1)	ENSP00000256460.3:n.912+92C>T
ENST00000302008.12:c.1048+110G>A (OGG1)	ENSP00000305527.8:n.1048+110G>A
ENST00000302036.11:c.948+2580G>A (OGG1)	ENSP00000306561.7:n.948+2580G>A
ENST00000349503.9:c.747+4511G>A (OGG1)	ENSP00000303132.6:n.747+4511G>A
ENST00000352937.5:c.463+4511G>A (OGG1)
ENST00000383826.9:c.566-6413G>A (OGG1)	ENSP00000373337.5:n.566-6413G>A
ENST00000397277.6:c.*793+276C>T (CAMK1)	ENSP00000380447.2:n.*793+276C>T
ENST00000421120.1:c.451+92C>T (CAMK1)
ENST00000426518.5:c.294+7447G>A (OGG1)
ENST00000449570.6:c.*32+110G>A (OGG1)	ENSP00000403598.2:n.*32+110G>A
ENST00000496534.1:n.987+92C>T (CAMK1)
ENST00000602976.1:n.2049G>A (OGG1)
NM_003656.4:c.912+92C>T (CAMK1)	NP_003647.1:n.912+92C>T
NM_016821.2:c.948+2580G>A (OGG1)	NP_058214.1:n.948+2580G>A
NM_016826.2:c.747+4511G>A (OGG1)	NP_058434.1:n.747+4511G>A
NM_016827.2:c.566-6413G>A (OGG1)	NP_058436.1:n.566-6413G>A
NM_016828.2:c.1048+110G>A (OGG1)	NP_058437.1:n.1048+110G>A
NM_016829.2:c.*32+110G>A (OGG1)	NP_058438.1:n.*32+110G>A
XM_005265516.1:c.912+92C>T (CAMK1)	XP_005265573.1:n.912+92C>T
XM_005265517.2:c.780+92C>T (CAMK1)	XP_005265574.1:n.780+92C>T
XM_011533760.1:c.948+2580G>A (OGG1)	XP_011532062.1:n.948+2580G>A
XR_940505.1:n.938+92C>T (CAMK1)
NM_001354650.1:c.797+2580G>A (OGG1)	NP_001341579.1:n.797+2580G>A
NM_001354651.1:c.898+2775G>A (OGG1)	NP_001341580.1:n.898+2775G>A
NM_001354652.1:c.850+110G>A (OGG1)	NP_001341581.1:n.850+110G>A
XM_005265516.2:c.912+92C>T (CAMK1)	XP_005265573.1:n.912+92C>T
XM_005265517.3:c.780+92C>T (CAMK1)	XP_005265574.1:n.780+92C>T
XM_011533760.2:c.948+2580G>A (OGG1)	XP_011532062.1:n.948+2580G>A
XM_017006494.2:c.850+110G>A (OGG1)	XP_016861983.1:n.850+110G>A
XM_017006496.2:c.948+2580G>A (OGG1)	XP_016861985.1:n.948+2580G>A
XM_017006497.2:c.850+110G>A (OGG1)	XP_016861986.1:n.850+110G>A
XM_017006499.2:c.797+2580G>A (OGG1)	XP_016861988.1:n.797+2580G>A
XM_017007354.1:c.780+92C>T (CAMK1)	XP_016862843.1:n.780+92C>T
XM_024453796.1:c.726+92C>T (CAMK1)	XP_024309564.1:n.726+92C>T
XR_940505.2:n.938+92C>T (CAMK1)
NM_003656.5:c.912+92C>T (CAMK1) MANE Select	NP_003647.1:n.912+92C>T
NM_001354650.2:c.797+2580G>A (OGG1)	NP_001341579.1:n.797+2580G>A
NM_001354651.2:c.898+2775G>A (OGG1)	NP_001341580.1:n.898+2775G>A
NM_001354652.2:c.850+110G>A (OGG1)	NP_001341581.1:n.850+110G>A
NM_016821.3:c.948+2580G>A (OGG1)	NP_058214.1:n.948+2580G>A
NM_016826.3:c.747+4511G>A (OGG1)	NP_058434.1:n.747+4511G>A
NM_016827.3:c.566-6413G>A (OGG1)	NP_058436.1:n.566-6413G>A
NM_016828.3:c.1048+110G>A (OGG1)	NP_058437.1:n.1048+110G>A
NM_016829.3:c.*32+110G>A (OGG1)	NP_058438.1:n.*32+110G>A