Canonical Allele Identifier: CA2590296863
Gene: PLA2G6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38120570_38120575del , CM000684.2:g.38120570_38120575del GRCh38
NC_000022.10:g.38516577_38516582del , CM000684.1:g.38516577_38516582del GRCh37
NC_000022.9:g.36846523_36846528del NCBI36
NG_007094.2:g.90117_90122del
NG_007094.3:g.99205_99210del

Transcript Alleles

HGVS Amino-acid Change
ENST00000332509.8:c.1742+185_1742+190del MANE Select ENSP00000333142.3:n.1742+185_1742+190del
ENST00000427114.6:c.1046+185_1046+190del ENSP00000407743.2:n.1046+185_1046+190del
ENST00000436218.6:c.*940+185_*940+190del ENSP00000401242.1:n.*940+185_*940+190del
ENST00000655142.1:c.*600+185_*600+190del ENSP00000499715.1:n.*600+185_*600+190del
ENST00000660610.1:c.1742+185_1742+190del ENSP00000499555.1:n.1742+185_1742+190del
ENST00000663895.1:c.1742+185_1742+190del ENSP00000499712.1:n.1742+185_1742+190del
ENST00000664587.1:c.1604+185_1604+190del ENSP00000499394.1:n.1604+185_1604+190del
ENST00000665987.1:c.*1481+185_*1481+190del ENSP00000499423.1:n.*1481+185_*1481+190del
ENST00000667521.1:c.1742+185_1742+190del ENSP00000499665.1:n.1742+185_1742+190del
ENST00000668208.1:n.1710+185_1710+190del
ENST00000668499.1:c.*1464+185_*1464+190del ENSP00000499626.1:n.*1464+185_*1464+190del
ENST00000668949.1:c.1580+185_1580+190del ENSP00000499711.1:n.1580+185_1580+190del
ENST00000671093.1:n.1674+185_1674+190del
ENST00000673413.1:c.*1411+185_*1411+190del ENSP00000500600.1:n.*1411+185_*1411+190del
ENST00000332509.7:c.1742+185_1742+190del ENSP00000333142.3:n.1742+185_1742+190del
ENST00000335539.7:c.1580+185_1580+190del ENSP00000335149.3:n.1580+185_1580+190del
ENST00000402064.5:c.1580+185_1580+190del ENSP00000386100.1:n.1580+185_1580+190del
ENST00000448094.5:c.*347+185_*347+190del ENSP00000407106.1:n.*347+185_*347+190del
ENST00000454670.1:c.387+185_387+190del
ENST00000496409.1:n.282+185_282+190del
NM_001004426.1:c.1580+185_1580+190del NP_001004426.1:n.1580+185_1580+190del
NM_001199562.1:c.1580+185_1580+190del NP_001186491.1:n.1580+185_1580+190del
NM_003560.2:c.1742+185_1742+190del NP_003551.2:n.1742+185_1742+190del
XM_005261764.1:c.1742+185_1742+190del XP_005261821.1:n.1742+185_1742+190del
XM_005261765.1:c.1742+185_1742+190del XP_005261822.1:n.1742+185_1742+190del
XM_005261766.1:c.1742+185_1742+190del XP_005261823.1:n.1742+185_1742+190del
XM_006724332.2:c.1742+185_1742+190del XP_006724395.1:n.1742+185_1742+190del
XM_011530422.1:c.1637+185_1637+190del XP_011528724.1:n.1637+185_1637+190del
XM_011530423.1:c.1208+185_1208+190del XP_011528725.1:n.1208+185_1208+190del
XM_011530424.1:c.1208+185_1208+190del XP_011528726.1:n.1208+185_1208+190del
XM_011530425.1:c.1208+185_1208+190del XP_011528727.1:n.1208+185_1208+190del
XM_011530426.1:c.1742+185_1742+190del XP_011528728.1:n.1742+185_1742+190del
XR_244390.1:n.1850+185_1850+190del
XR_430411.1:n.1902+185_1902+190del
XR_937937.1:n.1850+185_1850+190del
XR_937938.1:n.1936+185_1936+190del
XR_937939.1:n.1902+185_1902+190del
NM_001004426.2:c.1580+185_1580+190del NP_001004426.1:n.1580+185_1580+190del
NM_001199562.2:c.1580+185_1580+190del NP_001186491.1:n.1580+185_1580+190del
NM_001349864.1:c.1742+185_1742+190del NP_001336793.1:n.1742+185_1742+190del
NM_001349865.1:c.1580+185_1580+190del NP_001336794.1:n.1580+185_1580+190del
NM_001349866.1:c.1580+185_1580+190del NP_001336795.1:n.1580+185_1580+190del
NM_001349867.1:c.1208+185_1208+190del NP_001336796.1:n.1208+185_1208+190del
NM_001349868.1:c.1064+185_1064+190del NP_001336797.1:n.1064+185_1064+190del
NM_001349869.1:c.1046+185_1046+190del NP_001336798.1:n.1046+185_1046+190del
NM_003560.3:c.1742+185_1742+190del NP_003551.2:n.1742+185_1742+190del
XM_005261764.3:c.1742+185_1742+190del XP_005261821.1:n.1742+185_1742+190del
XM_005261765.2:c.1742+185_1742+190del XP_005261822.1:n.1742+185_1742+190del
XM_006724332.4:c.1742+185_1742+190del XP_006724395.1:n.1742+185_1742+190del
XM_011530426.3:c.1742+185_1742+190del XP_011528728.1:n.1742+185_1742+190del
XM_017028983.1:c.1046+185_1046+190del XP_016884472.1:n.1046+185_1046+190del
XM_017028986.2:c.1580+185_1580+190del XP_016884475.1:n.1580+185_1580+190del
XM_024452280.1:c.1208+185_1208+190del XP_024308048.1:n.1208+185_1208+190del
XM_024452281.1:c.1208+185_1208+190del XP_024308049.1:n.1208+185_1208+190del
XM_024452282.1:c.1208+185_1208+190del XP_024308050.1:n.1208+185_1208+190del
XM_024452283.1:c.1064+185_1064+190del XP_024308051.1:n.1064+185_1064+190del
XM_024452284.1:c.1046+185_1046+190del XP_024308052.1:n.1046+185_1046+190del
XM_024452285.1:c.1046+185_1046+190del XP_024308053.1:n.1046+185_1046+190del
XR_001755325.2:n.1834+185_1834+190del
XR_001755327.2:n.1920+185_1920+190del
XR_001755328.2:n.1886+185_1886+190del
XR_244390.3:n.1834+185_1834+190del
XR_937938.3:n.1920+185_1920+190del
XR_937939.3:n.1886+185_1886+190del
NM_001199562.3:c.1580+185_1580+190del NP_001186491.1:n.1580+185_1580+190del
NM_001349864.2:c.1742+185_1742+190del NP_001336793.1:n.1742+185_1742+190del
NM_001349865.2:c.1580+185_1580+190del NP_001336794.1:n.1580+185_1580+190del
NM_001349866.2:c.1580+185_1580+190del NP_001336795.1:n.1580+185_1580+190del
NM_001349867.2:c.1208+185_1208+190del NP_001336796.1:n.1208+185_1208+190del
NM_001349868.2:c.1064+185_1064+190del NP_001336797.1:n.1064+185_1064+190del
NM_001349869.2:c.1046+185_1046+190del NP_001336798.1:n.1046+185_1046+190del
NM_003560.4:c.1742+185_1742+190del MANE Select NP_003551.2:n.1742+185_1742+190del
NM_001004426.3:c.1580+185_1580+190del NP_001004426.1:n.1580+185_1580+190del