Canonical Allele Identifier: CA2832402997

Gene: PLA2G6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38115927_38115928insAAAGA , CM000684.2:g.38115927_38115928insAAAGA	GRCh38
NC_000022.10:g.38511934_38511935insAAAGA , CM000684.1:g.38511934_38511935insAAAGA	GRCh37
NC_000022.9:g.36841880_36841881insAAAGA	NCBI36
NG_007094.2:g.94763_94764insTCTTT
NG_007094.3:g.103851_103852insTCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1879+147_1879+148insTCTTT MANE Select	ENSP00000333142.3:n.1879+147_1879+148insTCTTT
ENST00000427114.6:c.1183+147_1183+148insTCTTT	ENSP00000407743.2:n.1183+147_1183+148insTCTTT
ENST00000436218.6:c.*1077+147_*1077+148insTCTTT	ENSP00000401242.1:n.*1077+147_*1077+148insTCTTT
ENST00000655142.1:c.*737+147_*737+148insTCTTT	ENSP00000499715.1:n.*737+147_*737+148insTCTTT
ENST00000660610.1:c.1879+147_1879+148insTCTTT	ENSP00000499555.1:n.1879+147_1879+148insTCTTT
ENST00000663895.1:c.1879+147_1879+148insTCTTT	ENSP00000499712.1:n.1879+147_1879+148insTCTTT
ENST00000664587.1:c.1741+147_1741+148insTCTTT	ENSP00000499394.1:n.1741+147_1741+148insTCTTT
ENST00000665987.1:c.*1618+147_*1618+148insTCTTT	ENSP00000499423.1:n.*1618+147_*1618+148insTCTTT
ENST00000667521.1:c.1879+147_1879+148insTCTTT	ENSP00000499665.1:n.1879+147_1879+148insTCTTT
ENST00000668499.1:c.*1601+147_*1601+148insTCTTT	ENSP00000499626.1:n.*1601+147_*1601+148insTCTTT
ENST00000668949.1:c.1717+147_1717+148insTCTTT	ENSP00000499711.1:n.1717+147_1717+148insTCTTT
ENST00000671093.1:n.1811+147_1811+148insTCTTT
ENST00000673413.1:c.*1548+147_*1548+148insTCTTT	ENSP00000500600.1:n.*1548+147_*1548+148insTCTTT
ENST00000332509.7:c.1879+147_1879+148insTCTTT	ENSP00000333142.3:n.1879+147_1879+148insTCTTT
ENST00000335539.7:c.1717+147_1717+148insTCTTT	ENSP00000335149.3:n.1717+147_1717+148insTCTTT
ENST00000402064.5:c.1717+147_1717+148insTCTTT	ENSP00000386100.1:n.1717+147_1717+148insTCTTT
ENST00000454670.1:c.615+147_615+148insTCTTT
ENST00000496409.1:n.420-79_420-78insTCTTT
NM_001004426.1:c.1717+147_1717+148insTCTTT	NP_001004426.1:n.1717+147_1717+148insTCTTT
NM_001199562.1:c.1717+147_1717+148insTCTTT	NP_001186491.1:n.1717+147_1717+148insTCTTT
NM_003560.2:c.1879+147_1879+148insTCTTT	NP_003551.2:n.1879+147_1879+148insTCTTT
XM_005261764.1:c.1879+147_1879+148insTCTTT	XP_005261821.1:n.1879+147_1879+148insTCTTT
XM_005261765.1:c.1879+147_1879+148insTCTTT	XP_005261822.1:n.1879+147_1879+148insTCTTT
XM_005261766.1:c.1879+147_1879+148insTCTTT	XP_005261823.1:n.1879+147_1879+148insTCTTT
XM_006724332.2:c.1879+147_1879+148insTCTTT	XP_006724395.1:n.1879+147_1879+148insTCTTT
XM_011530422.1:c.1774+147_1774+148insTCTTT	XP_011528724.1:n.1774+147_1774+148insTCTTT
XM_011530423.1:c.1345+147_1345+148insTCTTT	XP_011528725.1:n.1345+147_1345+148insTCTTT
XM_011530424.1:c.1345+147_1345+148insTCTTT	XP_011528726.1:n.1345+147_1345+148insTCTTT
XM_011530425.1:c.1345+147_1345+148insTCTTT	XP_011528727.1:n.1345+147_1345+148insTCTTT
XR_244390.1:n.1988-79_1988-78insTCTTT
XR_430411.1:n.2039+147_2039+148insTCTTT
XR_937937.1:n.2078+147_2078+148insTCTTT
XR_937938.1:n.2074-79_2074-78insTCTTT
XR_937939.1:n.2130+147_2130+148insTCTTT
NM_001004426.2:c.1717+147_1717+148insTCTTT	NP_001004426.1:n.1717+147_1717+148insTCTTT
NM_001199562.2:c.1717+147_1717+148insTCTTT	NP_001186491.1:n.1717+147_1717+148insTCTTT
NM_001349864.1:c.1879+147_1879+148insTCTTT	NP_001336793.1:n.1879+147_1879+148insTCTTT
NM_001349865.1:c.1717+147_1717+148insTCTTT	NP_001336794.1:n.1717+147_1717+148insTCTTT
NM_001349866.1:c.1717+147_1717+148insTCTTT	NP_001336795.1:n.1717+147_1717+148insTCTTT
NM_001349867.1:c.1345+147_1345+148insTCTTT	NP_001336796.1:n.1345+147_1345+148insTCTTT
NM_001349868.1:c.1201+147_1201+148insTCTTT	NP_001336797.1:n.1201+147_1201+148insTCTTT
NM_001349869.1:c.1183+147_1183+148insTCTTT	NP_001336798.1:n.1183+147_1183+148insTCTTT
NM_003560.3:c.1879+147_1879+148insTCTTT	NP_003551.2:n.1879+147_1879+148insTCTTT
XM_005261764.3:c.1879+147_1879+148insTCTTT	XP_005261821.1:n.1879+147_1879+148insTCTTT
XM_005261765.2:c.1879+147_1879+148insTCTTT	XP_005261822.1:n.1879+147_1879+148insTCTTT
XM_006724332.4:c.1879+147_1879+148insTCTTT	XP_006724395.1:n.1879+147_1879+148insTCTTT
XM_017028983.1:c.1183+147_1183+148insTCTTT	XP_016884472.1:n.1183+147_1183+148insTCTTT
XM_024452280.1:c.1345+147_1345+148insTCTTT	XP_024308048.1:n.1345+147_1345+148insTCTTT
XM_024452281.1:c.1345+147_1345+148insTCTTT	XP_024308049.1:n.1345+147_1345+148insTCTTT
XM_024452282.1:c.1345+147_1345+148insTCTTT	XP_024308050.1:n.1345+147_1345+148insTCTTT
XM_024452283.1:c.1201+147_1201+148insTCTTT	XP_024308051.1:n.1201+147_1201+148insTCTTT
XM_024452284.1:c.1183+147_1183+148insTCTTT	XP_024308052.1:n.1183+147_1183+148insTCTTT
XM_024452285.1:c.1183+147_1183+148insTCTTT	XP_024308053.1:n.1183+147_1183+148insTCTTT
XR_001755325.2:n.2062+147_2062+148insTCTTT
XR_001755327.2:n.2057+147_2057+148insTCTTT
XR_001755328.2:n.2023+147_2023+148insTCTTT
XR_244390.3:n.1972-79_1972-78insTCTTT
XR_937938.3:n.2058-79_2058-78insTCTTT
XR_937939.3:n.2114+147_2114+148insTCTTT
NM_001199562.3:c.1717+147_1717+148insTCTTT	NP_001186491.1:n.1717+147_1717+148insTCTTT
NM_001349864.2:c.1879+147_1879+148insTCTTT	NP_001336793.1:n.1879+147_1879+148insTCTTT
NM_001349865.2:c.1717+147_1717+148insTCTTT	NP_001336794.1:n.1717+147_1717+148insTCTTT
NM_001349866.2:c.1717+147_1717+148insTCTTT	NP_001336795.1:n.1717+147_1717+148insTCTTT
NM_001349867.2:c.1345+147_1345+148insTCTTT	NP_001336796.1:n.1345+147_1345+148insTCTTT
NM_001349868.2:c.1201+147_1201+148insTCTTT	NP_001336797.1:n.1201+147_1201+148insTCTTT
NM_001349869.2:c.1183+147_1183+148insTCTTT	NP_001336798.1:n.1183+147_1183+148insTCTTT
NM_003560.4:c.1879+147_1879+148insTCTTT MANE Select	NP_003551.2:n.1879+147_1879+148insTCTTT
NM_001004426.3:c.1717+147_1717+148insTCTTT	NP_001004426.1:n.1717+147_1717+148insTCTTT