Canonical Allele Identifier: CA2404672762
Gene: PLA2G6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38122967_38122968delinsTC , CM000684.2:g.38122967_38122968delinsTC GRCh38
NC_000022.10:g.38518974_38518975delinsTC , CM000684.1:g.38518974_38518975delinsTC GRCh37
NC_000022.9:g.36848920_36848921delinsTC NCBI36
NG_007094.2:g.87723_87724delinsGA
NG_007094.3:g.96811_96812delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000332509.8:c.1591+127_1591+128delinsGA MANE Select ENSP00000333142.3:n.1591+127_1591+128delinsGA
ENST00000427114.6:c.895+127_895+128delinsGA ENSP00000407743.2:n.895+127_895+128delinsGA
ENST00000436218.6:c.*789+127_*789+128delinsGA ENSP00000401242.1:n.*789+127_*789+128delinsGA
ENST00000655142.1:c.*449+127_*449+128delinsGA ENSP00000499715.1:n.*449+127_*449+128delinsGA
ENST00000660610.1:c.1591+127_1591+128delinsGA ENSP00000499555.1:n.1591+127_1591+128delinsGA
ENST00000663895.1:c.1591+127_1591+128delinsGA ENSP00000499712.1:n.1591+127_1591+128delinsGA
ENST00000664587.1:c.1453+127_1453+128delinsGA ENSP00000499394.1:n.1453+127_1453+128delinsGA
ENST00000665987.1:c.*1330+127_*1330+128delinsGA ENSP00000499423.1:n.*1330+127_*1330+128delinsGA
ENST00000667521.1:c.1591+127_1591+128delinsGA ENSP00000499665.1:n.1591+127_1591+128delinsGA
ENST00000668208.1:n.1559+127_1559+128delinsGA
ENST00000668499.1:c.*1313+127_*1313+128delinsGA ENSP00000499626.1:n.*1313+127_*1313+128delinsGA
ENST00000668949.1:c.1429+127_1429+128delinsGA ENSP00000499711.1:n.1429+127_1429+128delinsGA
ENST00000671093.1:n.1523+127_1523+128delinsGA
ENST00000673413.1:c.*1260+127_*1260+128delinsGA ENSP00000500600.1:n.*1260+127_*1260+128delinsGA
ENST00000332509.7:c.1591+127_1591+128delinsGA ENSP00000333142.3:n.1591+127_1591+128delinsGA
ENST00000335539.7:c.1429+127_1429+128delinsGA ENSP00000335149.3:n.1429+127_1429+128delinsGA
ENST00000402064.5:c.1429+127_1429+128delinsGA ENSP00000386100.1:n.1429+127_1429+128delinsGA
ENST00000448094.5:c.*196+127_*196+128delinsGA ENSP00000407106.1:n.*196+127_*196+128delinsGA
ENST00000454670.1:c.236+127_236+128delinsGA
ENST00000491986.1:n.602+127_602+128delinsGA
NM_001004426.1:c.1429+127_1429+128delinsGA NP_001004426.1:n.1429+127_1429+128delinsGA
NM_001199562.1:c.1429+127_1429+128delinsGA NP_001186491.1:n.1429+127_1429+128delinsGA
NM_003560.2:c.1591+127_1591+128delinsGA NP_003551.2:n.1591+127_1591+128delinsGA
XM_005261764.1:c.1591+127_1591+128delinsGA XP_005261821.1:n.1591+127_1591+128delinsGA
XM_005261765.1:c.1591+127_1591+128delinsGA XP_005261822.1:n.1591+127_1591+128delinsGA
XM_005261766.1:c.1591+127_1591+128delinsGA XP_005261823.1:n.1591+127_1591+128delinsGA
XM_006724332.2:c.1591+127_1591+128delinsGA XP_006724395.1:n.1591+127_1591+128delinsGA
XM_011530422.1:c.1486+127_1486+128delinsGA XP_011528724.1:n.1486+127_1486+128delinsGA
XM_011530423.1:c.1057+127_1057+128delinsGA XP_011528725.1:n.1057+127_1057+128delinsGA
XM_011530424.1:c.1057+127_1057+128delinsGA XP_011528726.1:n.1057+127_1057+128delinsGA
XM_011530425.1:c.1057+127_1057+128delinsGA XP_011528727.1:n.1057+127_1057+128delinsGA
XM_011530426.1:c.1591+127_1591+128delinsGA XP_011528728.1:n.1591+127_1591+128delinsGA
XR_244390.1:n.1699+127_1699+128delinsGA
XR_244392.1:n.1752+127_1752+128delinsGA
XR_430411.1:n.1751+127_1751+128delinsGA
XR_430412.1:n.1804+127_1804+128delinsGA
XR_937937.1:n.1699+127_1699+128delinsGA
XR_937938.1:n.1699+127_1699+128delinsGA
XR_937939.1:n.1751+127_1751+128delinsGA
XR_937940.1:n.1751+127_1751+128delinsGA
NM_001004426.2:c.1429+127_1429+128delinsGA NP_001004426.1:n.1429+127_1429+128delinsGA
NM_001199562.2:c.1429+127_1429+128delinsGA NP_001186491.1:n.1429+127_1429+128delinsGA
NM_001349864.1:c.1591+127_1591+128delinsGA NP_001336793.1:n.1591+127_1591+128delinsGA
NM_001349865.1:c.1429+127_1429+128delinsGA NP_001336794.1:n.1429+127_1429+128delinsGA
NM_001349866.1:c.1429+127_1429+128delinsGA NP_001336795.1:n.1429+127_1429+128delinsGA
NM_001349867.1:c.1057+127_1057+128delinsGA NP_001336796.1:n.1057+127_1057+128delinsGA
NM_001349868.1:c.913+127_913+128delinsGA NP_001336797.1:n.913+127_913+128delinsGA
NM_001349869.1:c.895+127_895+128delinsGA NP_001336798.1:n.895+127_895+128delinsGA
NM_003560.3:c.1591+127_1591+128delinsGA NP_003551.2:n.1591+127_1591+128delinsGA
XM_005261764.3:c.1591+127_1591+128delinsGA XP_005261821.1:n.1591+127_1591+128delinsGA
XM_005261765.2:c.1591+127_1591+128delinsGA XP_005261822.1:n.1591+127_1591+128delinsGA
XM_006724332.4:c.1591+127_1591+128delinsGA XP_006724395.1:n.1591+127_1591+128delinsGA
XM_011530426.3:c.1591+127_1591+128delinsGA XP_011528728.1:n.1591+127_1591+128delinsGA
XM_017028983.1:c.895+127_895+128delinsGA XP_016884472.1:n.895+127_895+128delinsGA
XM_017028986.2:c.1429+127_1429+128delinsGA XP_016884475.1:n.1429+127_1429+128delinsGA
XM_024452280.1:c.1057+127_1057+128delinsGA XP_024308048.1:n.1057+127_1057+128delinsGA
XM_024452281.1:c.1057+127_1057+128delinsGA XP_024308049.1:n.1057+127_1057+128delinsGA
XM_024452282.1:c.1057+127_1057+128delinsGA XP_024308050.1:n.1057+127_1057+128delinsGA
XM_024452283.1:c.913+127_913+128delinsGA XP_024308051.1:n.913+127_913+128delinsGA
XM_024452284.1:c.895+127_895+128delinsGA XP_024308052.1:n.895+127_895+128delinsGA
XM_024452285.1:c.895+127_895+128delinsGA XP_024308053.1:n.895+127_895+128delinsGA
XR_001755325.2:n.1683+127_1683+128delinsGA
XR_001755327.2:n.1683+127_1683+128delinsGA
XR_001755328.2:n.1735+127_1735+128delinsGA
XR_244390.3:n.1683+127_1683+128delinsGA
XR_937938.3:n.1683+127_1683+128delinsGA
XR_937939.3:n.1735+127_1735+128delinsGA
XR_937940.3:n.1735+127_1735+128delinsGA
NM_001199562.3:c.1429+127_1429+128delinsGA NP_001186491.1:n.1429+127_1429+128delinsGA
NM_001349864.2:c.1591+127_1591+128delinsGA NP_001336793.1:n.1591+127_1591+128delinsGA
NM_001349865.2:c.1429+127_1429+128delinsGA NP_001336794.1:n.1429+127_1429+128delinsGA
NM_001349866.2:c.1429+127_1429+128delinsGA NP_001336795.1:n.1429+127_1429+128delinsGA
NM_001349867.2:c.1057+127_1057+128delinsGA NP_001336796.1:n.1057+127_1057+128delinsGA
NM_001349868.2:c.913+127_913+128delinsGA NP_001336797.1:n.913+127_913+128delinsGA
NM_001349869.2:c.895+127_895+128delinsGA NP_001336798.1:n.895+127_895+128delinsGA
NM_003560.4:c.1591+127_1591+128delinsGA MANE Select NP_003551.2:n.1591+127_1591+128delinsGA
NM_001004426.3:c.1429+127_1429+128delinsGA NP_001004426.1:n.1429+127_1429+128delinsGA