Canonical Allele Identifier: CA10230870
Gene: PLA2G6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38126370C>T , CM000684.2:g.38126370C>T GRCh38
NC_000022.10:g.38522377C>T , CM000684.1:g.38522377C>T GRCh37
NC_000022.9:g.36852323C>T NCBI36
NG_007094.2:g.84321G>A
NG_007094.3:g.93409G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332509.8:c.1427+1G>A MANE Select ENSP00000333142.3:n.1427+1G>A
ENST00000427114.6:c.731+1G>A ENSP00000407743.2:n.731+1G>A
ENST00000436218.6:c.*625+1G>A ENSP00000401242.1:n.*625+1G>A
ENST00000655142.1:c.*285+1G>A ENSP00000499715.1:n.*285+1G>A
ENST00000660610.1:c.1427+1G>A ENSP00000499555.1:n.1427+1G>A
ENST00000663895.1:c.1427+1G>A ENSP00000499712.1:n.1427+1G>A
ENST00000664587.1:c.1289+1G>A ENSP00000499394.1:n.1289+1G>A
ENST00000665987.1:c.*1166+1G>A ENSP00000499423.1:n.*1166+1G>A
ENST00000667521.1:c.1427+1G>A ENSP00000499665.1:n.1427+1G>A
ENST00000668208.1:n.1395+1G>A
ENST00000668499.1:c.*1096+1G>A ENSP00000499626.1:n.*1096+1G>A
ENST00000668949.1:c.1265+1G>A ENSP00000499711.1:n.1265+1G>A
ENST00000671093.1:n.1359+1G>A
ENST00000673413.1:c.*1096+1G>A ENSP00000500600.1:n.*1096+1G>A
ENST00000332509.7:c.1427+1G>A ENSP00000333142.3:n.1427+1G>A
ENST00000335539.7:c.1265+1G>A ENSP00000335149.3:n.1265+1G>A
ENST00000402064.5:c.1265+1G>A ENSP00000386100.1:n.1265+1G>A
ENST00000448094.5:c.660+1G>A ENSP00000407106.1:n.660+1G>A
ENST00000454670.1:c.72+1G>A
ENST00000490473.1:n.546+1G>A
ENST00000491986.1:n.385+1G>A
NM_001004426.1:c.1265+1G>A NP_001004426.1:n.1265+1G>A
NM_001199562.1:c.1265+1G>A NP_001186491.1:n.1265+1G>A
NM_003560.2:c.1427+1G>A NP_003551.2:n.1427+1G>A
XM_005261764.1:c.1427+1G>A XP_005261821.1:n.1427+1G>A
XM_005261765.1:c.1427+1G>A XP_005261822.1:n.1427+1G>A
XM_005261766.1:c.1427+1G>A XP_005261823.1:n.1427+1G>A
XM_006724332.2:c.1427+1G>A XP_006724395.1:n.1427+1G>A
XM_011530422.1:c.1322+1G>A XP_011528724.1:n.1322+1G>A
XM_011530423.1:c.893+1G>A XP_011528725.1:n.893+1G>A
XM_011530424.1:c.893+1G>A XP_011528726.1:n.893+1G>A
XM_011530425.1:c.893+1G>A XP_011528727.1:n.893+1G>A
XM_011530426.1:c.1427+1G>A XP_011528728.1:n.1427+1G>A
XR_244390.1:n.1535+1G>A
XR_244392.1:n.1535+1G>A
XR_430411.1:n.1587+1G>A
XR_430412.1:n.1587+1G>A
XR_937937.1:n.1535+1G>A
XR_937938.1:n.1535+1G>A
XR_937939.1:n.1587+1G>A
XR_937940.1:n.1587+1G>A
NM_001004426.2:c.1265+1G>A NP_001004426.1:n.1265+1G>A
NM_001199562.2:c.1265+1G>A NP_001186491.1:n.1265+1G>A
NM_001349864.1:c.1427+1G>A NP_001336793.1:n.1427+1G>A
NM_001349865.1:c.1265+1G>A NP_001336794.1:n.1265+1G>A
NM_001349866.1:c.1265+1G>A NP_001336795.1:n.1265+1G>A
NM_001349867.1:c.893+1G>A NP_001336796.1:n.893+1G>A
NM_001349868.1:c.749+1G>A NP_001336797.1:n.749+1G>A
NM_001349869.1:c.731+1G>A NP_001336798.1:n.731+1G>A
NM_003560.3:c.1427+1G>A NP_003551.2:n.1427+1G>A
XM_005261764.3:c.1427+1G>A XP_005261821.1:n.1427+1G>A
XM_005261765.2:c.1427+1G>A XP_005261822.1:n.1427+1G>A
XM_006724332.4:c.1427+1G>A XP_006724395.1:n.1427+1G>A
XM_011530426.3:c.1427+1G>A XP_011528728.1:n.1427+1G>A
XM_017028983.1:c.731+1G>A XP_016884472.1:n.731+1G>A
XM_017028986.2:c.1265+1G>A XP_016884475.1:n.1265+1G>A
XM_017028987.2:c.1479+1G>A XP_016884476.1:n.1479+1G>A
XM_017028988.2:c.1427+1G>A XP_016884477.1:n.1427+1G>A
XM_024452280.1:c.893+1G>A XP_024308048.1:n.893+1G>A
XM_024452281.1:c.893+1G>A XP_024308049.1:n.893+1G>A
XM_024452282.1:c.893+1G>A XP_024308050.1:n.893+1G>A
XM_024452283.1:c.749+1G>A XP_024308051.1:n.749+1G>A
XM_024452284.1:c.731+1G>A XP_024308052.1:n.731+1G>A
XM_024452285.1:c.731+1G>A XP_024308053.1:n.731+1G>A
XR_001755325.2:n.1519+1G>A
XR_001755327.2:n.1519+1G>A
XR_001755328.2:n.1571+1G>A
XR_244390.3:n.1519+1G>A
XR_937938.3:n.1519+1G>A
XR_937939.3:n.1571+1G>A
XR_937940.3:n.1571+1G>A
NM_001199562.3:c.1265+1G>A NP_001186491.1:n.1265+1G>A
NM_001349864.2:c.1427+1G>A NP_001336793.1:n.1427+1G>A
NM_001349865.2:c.1265+1G>A NP_001336794.1:n.1265+1G>A
NM_001349866.2:c.1265+1G>A NP_001336795.1:n.1265+1G>A
NM_001349867.2:c.893+1G>A NP_001336796.1:n.893+1G>A
NM_001349868.2:c.749+1G>A NP_001336797.1:n.749+1G>A
NM_001349869.2:c.731+1G>A NP_001336798.1:n.731+1G>A
NM_003560.4:c.1427+1G>A MANE Select NP_003551.2:n.1427+1G>A
NM_001004426.3:c.1265+1G>A NP_001004426.1:n.1265+1G>A
Search 100 bp 5'
Search 100 bp 3'