Canonical Allele Identifier: CA2842038594

Gene: PLA2G6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38113610del , CM000684.2:g.38113610del	GRCh38
NC_000022.10:g.38509617del , CM000684.1:g.38509617del	GRCh37
NC_000022.9:g.36839563del	NCBI36
NG_007094.2:g.97084del
NG_033059.2:g.2063del
NG_007094.3:g.106172del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.2082del MANE Select	ENSP00000333142.3:p.Thr695GlnfsTer9
ENST00000436218.6:c.*1280del	ENSP00000401242.1:n.*1280del
ENST00000655142.1:c.*940del	ENSP00000499715.1:n.*940del
ENST00000660610.1:c.2082del	ENSP00000499555.1:p.Thr695GlnfsTer9
ENST00000663895.1:c.2082del	ENSP00000499712.1:p.Thr695GlnfsTer9
ENST00000664587.1:c.1944del	ENSP00000499394.1:p.Thr649GlnfsTer9
ENST00000665987.1:c.*1821del	ENSP00000499423.1:n.*1821del
ENST00000667521.1:c.2082del	ENSP00000499665.1:p.Thr695GlnfsTer9
ENST00000668499.1:c.*1941del	ENSP00000499626.1:n.*1941del
ENST00000668949.1:c.2124del	ENSP00000499711.1:p.Thr709GlnfsTer9
ENST00000671093.1:n.2014del
ENST00000673413.1:c.*1751del	ENSP00000500600.1:n.*1751del
ENST00000332509.7:c.2082del	ENSP00000333142.3:p.Thr695GlnfsTer9
ENST00000335539.7:c.1920del	ENSP00000335149.3:p.Thr641GlnfsTer9
ENST00000402064.5:c.1920del	ENSP00000386100.1:p.Thr641GlnfsTer9
ENST00000496409.1:n.790del
NM_001004426.1:c.1920del	NP_001004426.1:p.Thr641GlnfsTer9
NM_001199562.1:c.1920del	NP_001186491.1:p.Thr641GlnfsTer9
NM_003560.2:c.2082del	NP_003551.2:p.Thr695GlnfsTer9
XM_005261764.1:c.2082del	XP_005261821.1:p.Thr695GlnfsTer9
XM_005261765.1:c.2082del	XP_005261822.1:p.Thr695GlnfsTer9
XM_005261766.1:c.2082del	XP_005261823.1:p.Thr695GlnfsTer9
XM_006724332.2:c.2082del	XP_006724395.1:p.Thr695GlnfsTer9
XM_011530422.1:c.1977del	XP_011528724.1:p.Thr660GlnfsTer9
XM_011530423.1:c.1548del	XP_011528725.1:p.Thr517GlnfsTer9
XM_011530424.1:c.1548del	XP_011528726.1:p.Thr517GlnfsTer9
XM_011530425.1:c.1548del	XP_011528727.1:p.Thr517GlnfsTer9
XR_244390.1:n.2358del
XR_430411.1:n.2242del
XR_937938.1:n.2444del
NM_001004426.2:c.1920del	NP_001004426.1:p.Thr641GlnfsTer9
NM_001199562.2:c.1920del	NP_001186491.1:p.Thr641GlnfsTer9
NM_001349864.1:c.2082del	NP_001336793.1:p.Thr695GlnfsTer9
NM_001349865.1:c.1920del	NP_001336794.1:p.Thr641GlnfsTer9
NM_001349866.1:c.1920del	NP_001336795.1:p.Thr641GlnfsTer9
NM_001349867.1:c.1548del	NP_001336796.1:p.Thr517GlnfsTer9
NM_001349868.1:c.1404del	NP_001336797.1:p.Thr469GlnfsTer9
NM_001349869.1:c.1386del	NP_001336798.1:p.Thr463GlnfsTer9
NM_003560.3:c.2082del	NP_003551.2:p.Thr695GlnfsTer9
XM_005261764.3:c.2082del	XP_005261821.1:p.Thr695GlnfsTer9
XM_005261765.2:c.2082del	XP_005261822.1:p.Thr695GlnfsTer9
XM_006724332.4:c.2082del	XP_006724395.1:p.Thr695GlnfsTer9
XM_017028983.1:c.1386del	XP_016884472.1:p.Thr463GlnfsTer9
XM_024452280.1:c.1548del	XP_024308048.1:p.Thr517GlnfsTer9
XM_024452281.1:c.1548del	XP_024308049.1:p.Thr517GlnfsTer9
XM_024452282.1:c.1548del	XP_024308050.1:p.Thr517GlnfsTer9
XM_024452283.1:c.1404del	XP_024308051.1:p.Thr469GlnfsTer9
XM_024452284.1:c.1386del	XP_024308052.1:p.Thr463GlnfsTer9
XM_024452285.1:c.1386del	XP_024308053.1:p.Thr463GlnfsTer9
XR_001755325.2:n.2265del
XR_001755327.2:n.2260del
XR_001755328.2:n.2226del
XR_244390.3:n.2342del
XR_937938.3:n.2428del
NM_001199562.3:c.1920del	NP_001186491.1:p.Thr641GlnfsTer9
NM_001349864.2:c.2082del	NP_001336793.1:p.Thr695GlnfsTer9
NM_001349865.2:c.1920del	NP_001336794.1:p.Thr641GlnfsTer9
NM_001349866.2:c.1920del	NP_001336795.1:p.Thr641GlnfsTer9
NM_001349867.2:c.1548del	NP_001336796.1:p.Thr517GlnfsTer9
NM_001349868.2:c.1404del	NP_001336797.1:p.Thr469GlnfsTer9
NM_001349869.2:c.1386del	NP_001336798.1:p.Thr463GlnfsTer9
NM_003560.4:c.2082del MANE Select	NP_003551.2:p.Thr695GlnfsTer9
NM_001004426.3:c.1920del	NP_001004426.1:p.Thr641GlnfsTer9