Canonical Allele Identifier: CA204738
Gene: PLA2G6 HGNC NCBI

Linked Data

ClinVar Variation Id: 208712
ClinVar RCV Id: RCV000190729
dbSNP Id: rs797044903

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38132883_38132889del , CM000684.2:g.38132883_38132889del GRCh38
NC_000022.10:g.38528890_38528896del , CM000684.1:g.38528890_38528896del GRCh37
NC_000022.9:g.36858836_36858842del NCBI36
NG_007094.2:g.77802_77808del
NG_007094.3:g.86890_86896del

Transcript Alleles

HGVS Amino-acid Change
ENST00000332509.8:c.1019_1025del MANE Select ENSP00000333142.3:p.Gly340AlafsTer24
ENST00000427114.6:c.485_491del ENSP00000407743.2:p.Gly162AlafsTer24
ENST00000436218.6:c.*379_*385del ENSP00000401242.1:n.*379_*385del
ENST00000655142.1:c.831_837del ENSP00000499715.1:p.Gly278AlafsTer?
ENST00000660610.1:c.1019_1025del ENSP00000499555.1:p.Gly340AlafsTer24
ENST00000663895.1:c.1019_1025del ENSP00000499712.1:p.Gly340AlafsTer24
ENST00000664587.1:c.1019_1025del ENSP00000499394.1:p.Gly340AlafsTer24
ENST00000665987.1:c.*920_*926del ENSP00000499423.1:n.*920_*926del
ENST00000667521.1:c.1019_1025del ENSP00000499665.1:p.Gly340AlafsTer24
ENST00000668208.1:n.1149_1155del
ENST00000668499.1:c.*850_*856del ENSP00000499626.1:n.*850_*856del
ENST00000668949.1:c.1019_1025del ENSP00000499711.1:p.Gly340AlafsTer24
ENST00000671093.1:n.1113_1119del
ENST00000673413.1:c.*850_*856del ENSP00000500600.1:n.*850_*856del
ENST00000332509.7:c.1019_1025del ENSP00000333142.3:p.Gly340AlafsTer24
ENST00000335539.7:c.1019_1025del ENSP00000335149.3:p.Gly340AlafsTer24
ENST00000402064.5:c.1019_1025del ENSP00000386100.1:p.Gly340AlafsTer24
ENST00000427114.5:c.433_439del
ENST00000427453.5:c.274_280del
ENST00000448094.5:c.200_206del ENSP00000407106.1:p.Gly67AlafsTer24
ENST00000452542.5:c.511_517del
ENST00000471636.5:n.413-6362_413-6356del
NM_001004426.1:c.1019_1025del NP_001004426.1:p.Gly340AlafsTer24
NM_001199562.1:c.1019_1025del NP_001186491.1:p.Gly340AlafsTer24
NM_003560.2:c.1019_1025del NP_003551.2:p.Gly340AlafsTer24
XM_005261764.1:c.1019_1025del XP_005261821.1:p.Gly340AlafsTer24
XM_005261765.1:c.1019_1025del XP_005261822.1:p.Gly340AlafsTer24
XM_005261766.1:c.1019_1025del XP_005261823.1:p.Gly340AlafsTer24
XM_005261771.3:c.1019_1025del XP_005261828.1:p.Gly340AlafsTer24
XM_006724332.2:c.1019_1025del XP_006724395.1:p.Gly340AlafsTer24
XM_011530422.1:c.914_920del XP_011528724.1:p.Gly305AlafsTer24
XM_011530423.1:c.485_491del XP_011528725.1:p.Gly162AlafsTer24
XM_011530424.1:c.485_491del XP_011528726.1:p.Gly162AlafsTer24
XM_011530425.1:c.485_491del XP_011528727.1:p.Gly162AlafsTer24
XM_011530426.1:c.1019_1025del XP_011528728.1:p.Gly340AlafsTer24
XM_011530427.1:c.914_920del XP_011528729.1:p.Gly305AlafsTer24
XM_011530428.1:c.1019_1025del XP_011528730.1:p.Gly340AlafsTer29
XR_244390.1:n.1127_1133del
XR_244392.1:n.1127_1133del
XR_430411.1:n.1127_1133del
XR_430412.1:n.1127_1133del
XR_937937.1:n.1127_1133del
XR_937938.1:n.1127_1133del
XR_937939.1:n.1127_1133del
XR_937940.1:n.1127_1133del
NM_001004426.2:c.1019_1025del NP_001004426.1:p.Gly340AlafsTer24
NM_001199562.2:c.1019_1025del NP_001186491.1:p.Gly340AlafsTer24
NM_001349864.1:c.1019_1025del NP_001336793.1:p.Gly340AlafsTer24
NM_001349865.1:c.1019_1025del NP_001336794.1:p.Gly340AlafsTer24
NM_001349866.1:c.1019_1025del NP_001336795.1:p.Gly340AlafsTer24
NM_001349867.1:c.485_491del NP_001336796.1:p.Gly162AlafsTer24
NM_001349868.1:c.341_347del NP_001336797.1:p.Gly114AlafsTer24
NM_001349869.1:c.485_491del NP_001336798.1:p.Gly162AlafsTer24
NM_003560.3:c.1019_1025del NP_003551.2:p.Gly340AlafsTer24
XM_005261764.3:c.1019_1025del XP_005261821.1:p.Gly340AlafsTer24
XM_005261765.2:c.1019_1025del XP_005261822.1:p.Gly340AlafsTer24
XM_006724332.4:c.1019_1025del XP_006724395.1:p.Gly340AlafsTer24
XM_011530426.3:c.1019_1025del XP_011528728.1:p.Gly340AlafsTer24
XM_017028983.1:c.485_491del XP_016884472.1:p.Gly162AlafsTer24
XM_017028986.2:c.1019_1025del XP_016884475.1:p.Gly340AlafsTer24
XM_017028987.2:c.1019_1025del XP_016884476.1:p.Gly340AlafsTer24
XM_017028988.2:c.1019_1025del XP_016884477.1:p.Gly340AlafsTer24
XM_024452280.1:c.485_491del XP_024308048.1:p.Gly162AlafsTer24
XM_024452281.1:c.485_491del XP_024308049.1:p.Gly162AlafsTer24
XM_024452282.1:c.485_491del XP_024308050.1:p.Gly162AlafsTer24
XM_024452283.1:c.341_347del XP_024308051.1:p.Gly114AlafsTer24
XM_024452284.1:c.485_491del XP_024308052.1:p.Gly162AlafsTer24
XM_024452285.1:c.485_491del XP_024308053.1:p.Gly162AlafsTer24
XR_001755325.2:n.1111_1117del
XR_001755327.2:n.1111_1117del
XR_001755328.2:n.1111_1117del
XR_244390.3:n.1111_1117del
XR_937938.3:n.1111_1117del
XR_937939.3:n.1111_1117del
XR_937940.3:n.1111_1117del
NM_001199562.3:c.1019_1025del NP_001186491.1:p.Gly340AlafsTer24
NM_001349864.2:c.1019_1025del NP_001336793.1:p.Gly340AlafsTer24
NM_001349865.2:c.1019_1025del NP_001336794.1:p.Gly340AlafsTer24
NM_001349866.2:c.1019_1025del NP_001336795.1:p.Gly340AlafsTer24
NM_001349867.2:c.485_491del NP_001336796.1:p.Gly162AlafsTer24
NM_001349868.2:c.341_347del NP_001336797.1:p.Gly114AlafsTer24
NM_001349869.2:c.485_491del NP_001336798.1:p.Gly162AlafsTer24
NM_003560.4:c.1019_1025del MANE Select NP_003551.2:p.Gly340AlafsTer24
NM_001004426.3:c.1019_1025del NP_001004426.1:p.Gly340AlafsTer24