Canonical Allele Identifier: CA2404672773
Gene: PLA2G6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38122985_38122988delinsCCCT , CM000684.2:g.38122985_38122988delinsCCCT GRCh38
NC_000022.10:g.38518992_38518995delinsCCCT , CM000684.1:g.38518992_38518995delinsCCCT GRCh37
NC_000022.9:g.36848938_36848941delinsCCCT NCBI36
NG_007094.2:g.87703_87706delinsAGGG
NG_007094.3:g.96791_96794delinsAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000332509.8:c.1591+107_1591+110delinsAGGG MANE Select ENSP00000333142.3:n.1591+107_1591+110delinsAGGG
ENST00000427114.6:c.895+107_895+110delinsAGGG ENSP00000407743.2:n.895+107_895+110delinsAGGG
ENST00000436218.6:c.*789+107_*789+110delinsAGGG ENSP00000401242.1:n.*789+107_*789+110delinsAGGG
ENST00000655142.1:c.*449+107_*449+110delinsAGGG ENSP00000499715.1:n.*449+107_*449+110delinsAGGG
ENST00000660610.1:c.1591+107_1591+110delinsAGGG ENSP00000499555.1:n.1591+107_1591+110delinsAGGG
ENST00000663895.1:c.1591+107_1591+110delinsAGGG ENSP00000499712.1:n.1591+107_1591+110delinsAGGG
ENST00000664587.1:c.1453+107_1453+110delinsAGGG ENSP00000499394.1:n.1453+107_1453+110delinsAGGG
ENST00000665987.1:c.*1330+107_*1330+110delinsAGGG ENSP00000499423.1:n.*1330+107_*1330+110delinsAGGG
ENST00000667521.1:c.1591+107_1591+110delinsAGGG ENSP00000499665.1:n.1591+107_1591+110delinsAGGG
ENST00000668208.1:n.1559+107_1559+110delinsAGGG
ENST00000668499.1:c.*1313+107_*1313+110delinsAGGG ENSP00000499626.1:n.*1313+107_*1313+110delinsAGGG
ENST00000668949.1:c.1429+107_1429+110delinsAGGG ENSP00000499711.1:n.1429+107_1429+110delinsAGGG
ENST00000671093.1:n.1523+107_1523+110delinsAGGG
ENST00000673413.1:c.*1260+107_*1260+110delinsAGGG ENSP00000500600.1:n.*1260+107_*1260+110delinsAGGG
ENST00000332509.7:c.1591+107_1591+110delinsAGGG ENSP00000333142.3:n.1591+107_1591+110delinsAGGG
ENST00000335539.7:c.1429+107_1429+110delinsAGGG ENSP00000335149.3:n.1429+107_1429+110delinsAGGG
ENST00000402064.5:c.1429+107_1429+110delinsAGGG ENSP00000386100.1:n.1429+107_1429+110delinsAGGG
ENST00000448094.5:c.*196+107_*196+110delinsAGGG ENSP00000407106.1:n.*196+107_*196+110delinsAGGG
ENST00000454670.1:c.236+107_236+110delinsAGGG
ENST00000491986.1:n.602+107_602+110delinsAGGG
NM_001004426.1:c.1429+107_1429+110delinsAGGG NP_001004426.1:n.1429+107_1429+110delinsAGGG
NM_001199562.1:c.1429+107_1429+110delinsAGGG NP_001186491.1:n.1429+107_1429+110delinsAGGG
NM_003560.2:c.1591+107_1591+110delinsAGGG NP_003551.2:n.1591+107_1591+110delinsAGGG
XM_005261764.1:c.1591+107_1591+110delinsAGGG XP_005261821.1:n.1591+107_1591+110delinsAGGG
XM_005261765.1:c.1591+107_1591+110delinsAGGG XP_005261822.1:n.1591+107_1591+110delinsAGGG
XM_005261766.1:c.1591+107_1591+110delinsAGGG XP_005261823.1:n.1591+107_1591+110delinsAGGG
XM_006724332.2:c.1591+107_1591+110delinsAGGG XP_006724395.1:n.1591+107_1591+110delinsAGGG
XM_011530422.1:c.1486+107_1486+110delinsAGGG XP_011528724.1:n.1486+107_1486+110delinsAGGG
XM_011530423.1:c.1057+107_1057+110delinsAGGG XP_011528725.1:n.1057+107_1057+110delinsAGGG
XM_011530424.1:c.1057+107_1057+110delinsAGGG XP_011528726.1:n.1057+107_1057+110delinsAGGG
XM_011530425.1:c.1057+107_1057+110delinsAGGG XP_011528727.1:n.1057+107_1057+110delinsAGGG
XM_011530426.1:c.1591+107_1591+110delinsAGGG XP_011528728.1:n.1591+107_1591+110delinsAGGG
XR_244390.1:n.1699+107_1699+110delinsAGGG
XR_244392.1:n.1752+107_1752+110delinsAGGG
XR_430411.1:n.1751+107_1751+110delinsAGGG
XR_430412.1:n.1804+107_1804+110delinsAGGG
XR_937937.1:n.1699+107_1699+110delinsAGGG
XR_937938.1:n.1699+107_1699+110delinsAGGG
XR_937939.1:n.1751+107_1751+110delinsAGGG
XR_937940.1:n.1751+107_1751+110delinsAGGG
NM_001004426.2:c.1429+107_1429+110delinsAGGG NP_001004426.1:n.1429+107_1429+110delinsAGGG
NM_001199562.2:c.1429+107_1429+110delinsAGGG NP_001186491.1:n.1429+107_1429+110delinsAGGG
NM_001349864.1:c.1591+107_1591+110delinsAGGG NP_001336793.1:n.1591+107_1591+110delinsAGGG
NM_001349865.1:c.1429+107_1429+110delinsAGGG NP_001336794.1:n.1429+107_1429+110delinsAGGG
NM_001349866.1:c.1429+107_1429+110delinsAGGG NP_001336795.1:n.1429+107_1429+110delinsAGGG
NM_001349867.1:c.1057+107_1057+110delinsAGGG NP_001336796.1:n.1057+107_1057+110delinsAGGG
NM_001349868.1:c.913+107_913+110delinsAGGG NP_001336797.1:n.913+107_913+110delinsAGGG
NM_001349869.1:c.895+107_895+110delinsAGGG NP_001336798.1:n.895+107_895+110delinsAGGG
NM_003560.3:c.1591+107_1591+110delinsAGGG NP_003551.2:n.1591+107_1591+110delinsAGGG
XM_005261764.3:c.1591+107_1591+110delinsAGGG XP_005261821.1:n.1591+107_1591+110delinsAGGG
XM_005261765.2:c.1591+107_1591+110delinsAGGG XP_005261822.1:n.1591+107_1591+110delinsAGGG
XM_006724332.4:c.1591+107_1591+110delinsAGGG XP_006724395.1:n.1591+107_1591+110delinsAGGG
XM_011530426.3:c.1591+107_1591+110delinsAGGG XP_011528728.1:n.1591+107_1591+110delinsAGGG
XM_017028983.1:c.895+107_895+110delinsAGGG XP_016884472.1:n.895+107_895+110delinsAGGG
XM_017028986.2:c.1429+107_1429+110delinsAGGG XP_016884475.1:n.1429+107_1429+110delinsAGGG
XM_024452280.1:c.1057+107_1057+110delinsAGGG XP_024308048.1:n.1057+107_1057+110delinsAGGG
XM_024452281.1:c.1057+107_1057+110delinsAGGG XP_024308049.1:n.1057+107_1057+110delinsAGGG
XM_024452282.1:c.1057+107_1057+110delinsAGGG XP_024308050.1:n.1057+107_1057+110delinsAGGG
XM_024452283.1:c.913+107_913+110delinsAGGG XP_024308051.1:n.913+107_913+110delinsAGGG
XM_024452284.1:c.895+107_895+110delinsAGGG XP_024308052.1:n.895+107_895+110delinsAGGG
XM_024452285.1:c.895+107_895+110delinsAGGG XP_024308053.1:n.895+107_895+110delinsAGGG
XR_001755325.2:n.1683+107_1683+110delinsAGGG
XR_001755327.2:n.1683+107_1683+110delinsAGGG
XR_001755328.2:n.1735+107_1735+110delinsAGGG
XR_244390.3:n.1683+107_1683+110delinsAGGG
XR_937938.3:n.1683+107_1683+110delinsAGGG
XR_937939.3:n.1735+107_1735+110delinsAGGG
XR_937940.3:n.1735+107_1735+110delinsAGGG
NM_001199562.3:c.1429+107_1429+110delinsAGGG NP_001186491.1:n.1429+107_1429+110delinsAGGG
NM_001349864.2:c.1591+107_1591+110delinsAGGG NP_001336793.1:n.1591+107_1591+110delinsAGGG
NM_001349865.2:c.1429+107_1429+110delinsAGGG NP_001336794.1:n.1429+107_1429+110delinsAGGG
NM_001349866.2:c.1429+107_1429+110delinsAGGG NP_001336795.1:n.1429+107_1429+110delinsAGGG
NM_001349867.2:c.1057+107_1057+110delinsAGGG NP_001336796.1:n.1057+107_1057+110delinsAGGG
NM_001349868.2:c.913+107_913+110delinsAGGG NP_001336797.1:n.913+107_913+110delinsAGGG
NM_001349869.2:c.895+107_895+110delinsAGGG NP_001336798.1:n.895+107_895+110delinsAGGG
NM_003560.4:c.1591+107_1591+110delinsAGGG MANE Select NP_003551.2:n.1591+107_1591+110delinsAGGG
NM_001004426.3:c.1429+107_1429+110delinsAGGG NP_001004426.1:n.1429+107_1429+110delinsAGGG