Canonical Allele Identifier: CA1025607423
Gene: PLA2G6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2869885
dbSNP Id: rs2087627455

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38123231_38123233del , CM000684.2:g.38123231_38123233del GRCh38
NC_000022.10:g.38519238_38519240del , CM000684.1:g.38519238_38519240del GRCh37
NC_000022.9:g.36849184_36849186del NCBI36
NG_007094.2:g.87465_87467del
NG_007094.3:g.96553_96555del

Transcript Alleles

HGVS Amino-acid Change
ENST00000332509.8:c.1460_1462del MANE Select ENSP00000333142.3:p.Gly487del
ENST00000427114.6:c.764_766del ENSP00000407743.2:p.Gly255del
ENST00000436218.6:c.*658_*660del ENSP00000401242.1:n.*658_*660del
ENST00000655142.1:c.*318_*320del ENSP00000499715.1:n.*318_*320del
ENST00000660610.1:c.1460_1462del ENSP00000499555.1:p.Gly487del
ENST00000663895.1:c.1460_1462del ENSP00000499712.1:p.Gly487del
ENST00000664587.1:c.1322_1324del ENSP00000499394.1:p.Gly441del
ENST00000665987.1:c.*1199_*1201del ENSP00000499423.1:n.*1199_*1201del
ENST00000667521.1:c.1460_1462del ENSP00000499665.1:p.Gly487del
ENST00000668208.1:n.1428_1430del
ENST00000668499.1:c.*1182_*1184del ENSP00000499626.1:n.*1182_*1184del
ENST00000668949.1:c.1298_1300del ENSP00000499711.1:p.Gly433del
ENST00000671093.1:n.1392_1394del
ENST00000673413.1:c.*1129_*1131del ENSP00000500600.1:n.*1129_*1131del
ENST00000332509.7:c.1460_1462del ENSP00000333142.3:p.Gly487del
ENST00000335539.7:c.1298_1300del ENSP00000335149.3:p.Gly433del
ENST00000402064.5:c.1298_1300del ENSP00000386100.1:p.Gly433del
ENST00000448094.5:c.*65_*67del ENSP00000407106.1:n.*65_*67del
ENST00000454670.1:c.105_107del
ENST00000490473.1:n.579_581del
ENST00000491986.1:n.471_473del
NM_001004426.1:c.1298_1300del NP_001004426.1:p.Gly433del
NM_001199562.1:c.1298_1300del NP_001186491.1:p.Gly433del
NM_003560.2:c.1460_1462del NP_003551.2:p.Gly487del
XM_005261764.1:c.1460_1462del XP_005261821.1:p.Gly487del
XM_005261765.1:c.1460_1462del XP_005261822.1:p.Gly487del
XM_005261766.1:c.1460_1462del XP_005261823.1:p.Gly487del
XM_006724332.2:c.1460_1462del XP_006724395.1:p.Gly487del
XM_011530422.1:c.1355_1357del XP_011528724.1:p.Gly452del
XM_011530423.1:c.926_928del XP_011528725.1:p.Gly309del
XM_011530424.1:c.926_928del XP_011528726.1:p.Gly309del
XM_011530425.1:c.926_928del XP_011528727.1:p.Gly309del
XM_011530426.1:c.1460_1462del XP_011528728.1:p.Gly487del
XR_244390.1:n.1568_1570del
XR_244392.1:n.1621_1623del
XR_430411.1:n.1620_1622del
XR_430412.1:n.1673_1675del
XR_937937.1:n.1568_1570del
XR_937938.1:n.1568_1570del
XR_937939.1:n.1620_1622del
XR_937940.1:n.1620_1622del
NM_001004426.2:c.1298_1300del NP_001004426.1:p.Gly433del
NM_001199562.2:c.1298_1300del NP_001186491.1:p.Gly433del
NM_001349864.1:c.1460_1462del NP_001336793.1:p.Gly487del
NM_001349865.1:c.1298_1300del NP_001336794.1:p.Gly433del
NM_001349866.1:c.1298_1300del NP_001336795.1:p.Gly433del
NM_001349867.1:c.926_928del NP_001336796.1:p.Gly309del
NM_001349868.1:c.782_784del NP_001336797.1:p.Gly261del
NM_001349869.1:c.764_766del NP_001336798.1:p.Gly255del
NM_003560.3:c.1460_1462del NP_003551.2:p.Gly487del
XM_005261764.3:c.1460_1462del XP_005261821.1:p.Gly487del
XM_005261765.2:c.1460_1462del XP_005261822.1:p.Gly487del
XM_006724332.4:c.1460_1462del XP_006724395.1:p.Gly487del
XM_011530426.3:c.1460_1462del XP_011528728.1:p.Gly487del
XM_017028983.1:c.764_766del XP_016884472.1:p.Gly255del
XM_017028986.2:c.1298_1300del XP_016884475.1:p.Gly433del
XM_017028987.2:c.*65_*67del XP_016884476.1:n.*65_*67del
XM_017028988.2:c.*73_*75del XP_016884477.1:n.*73_*75del
XM_024452280.1:c.926_928del XP_024308048.1:p.Gly309del
XM_024452281.1:c.926_928del XP_024308049.1:p.Gly309del
XM_024452282.1:c.926_928del XP_024308050.1:p.Gly309del
XM_024452283.1:c.782_784del XP_024308051.1:p.Gly261del
XM_024452284.1:c.764_766del XP_024308052.1:p.Gly255del
XM_024452285.1:c.764_766del XP_024308053.1:p.Gly255del
XR_001755325.2:n.1552_1554del
XR_001755327.2:n.1552_1554del
XR_001755328.2:n.1604_1606del
XR_244390.3:n.1552_1554del
XR_937938.3:n.1552_1554del
XR_937939.3:n.1604_1606del
XR_937940.3:n.1604_1606del
NM_001199562.3:c.1298_1300del NP_001186491.1:p.Gly433del
NM_001349864.2:c.1460_1462del NP_001336793.1:p.Gly487del
NM_001349865.2:c.1298_1300del NP_001336794.1:p.Gly433del
NM_001349866.2:c.1298_1300del NP_001336795.1:p.Gly433del
NM_001349867.2:c.926_928del NP_001336796.1:p.Gly309del
NM_001349868.2:c.782_784del NP_001336797.1:p.Gly261del
NM_001349869.2:c.764_766del NP_001336798.1:p.Gly255del
NM_003560.4:c.1460_1462del MANE Select NP_003551.2:p.Gly487del
NM_001004426.3:c.1298_1300del NP_001004426.1:p.Gly433del