Canonical Allele Identifier: CA2404669661

Gene: PLA2G6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38116114T= , CM000684.2:g.38116114T=	GRCh38
NC_000022.10:g.38512121T= , CM000684.1:g.38512121T=	GRCh37
NC_000022.9:g.36842067T=	NCBI36
NG_007094.2:g.94577A=
NG_007094.3:g.103665A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1840A= MANE Select	ENSP00000333142.3:p.Asn614=
ENST00000427114.6:c.1144A=	ENSP00000407743.2:p.Asn382=
ENST00000436218.6:c.*1038A=	ENSP00000401242.1:n.*1038A=
ENST00000655142.1:c.*698A=	ENSP00000499715.1:n.*698A=
ENST00000660610.1:c.1840A=	ENSP00000499555.1:p.Asn614=
ENST00000663895.1:c.1840A=	ENSP00000499712.1:p.Asn614=
ENST00000664587.1:c.1702A=	ENSP00000499394.1:p.Asn568=
ENST00000665987.1:c.*1579A=	ENSP00000499423.1:n.*1579A=
ENST00000667521.1:c.1840A=	ENSP00000499665.1:p.Asn614=
ENST00000668499.1:c.*1562A=	ENSP00000499626.1:n.*1562A=
ENST00000668949.1:c.1678A=	ENSP00000499711.1:p.Asn560=
ENST00000671093.1:n.1772A=
ENST00000673413.1:c.*1509A=	ENSP00000500600.1:n.*1509A=
ENST00000332509.7:c.1840A=	ENSP00000333142.3:p.Asn614=
ENST00000335539.7:c.1678A=	ENSP00000335149.3:p.Asn560=
ENST00000402064.5:c.1678A=	ENSP00000386100.1:p.Asn560=
ENST00000448094.5:c.*445A=	ENSP00000407106.1:n.*445A=
ENST00000454670.1:c.576A=
ENST00000496409.1:n.380A=
NM_001004426.1:c.1678A=	NP_001004426.1:p.Asn560=
NM_001199562.1:c.1678A=	NP_001186491.1:p.Asn560=
NM_003560.2:c.1840A=	NP_003551.2:p.Asn614=
XM_005261764.1:c.1840A=	XP_005261821.1:p.Asn614=
XM_005261765.1:c.1840A=	XP_005261822.1:p.Asn614=
XM_005261766.1:c.1840A=	XP_005261823.1:p.Asn614=
XM_006724332.2:c.1840A=	XP_006724395.1:p.Asn614=
XM_011530422.1:c.1735A=	XP_011528724.1:p.Asn579=
XM_011530423.1:c.1306A=	XP_011528725.1:p.Asn436=
XM_011530424.1:c.1306A=	XP_011528726.1:p.Asn436=
XM_011530425.1:c.1306A=	XP_011528727.1:p.Asn436=
XR_244390.1:n.1948A=
XR_430411.1:n.2000A=
XR_937937.1:n.2039A=
XR_937938.1:n.2034A=
XR_937939.1:n.2091A=
NM_001004426.2:c.1678A=	NP_001004426.1:p.Asn560=
NM_001199562.2:c.1678A=	NP_001186491.1:p.Asn560=
NM_001349864.1:c.1840A=	NP_001336793.1:p.Asn614=
NM_001349865.1:c.1678A=	NP_001336794.1:p.Asn560=
NM_001349866.1:c.1678A=	NP_001336795.1:p.Asn560=
NM_001349867.1:c.1306A=	NP_001336796.1:p.Asn436=
NM_001349868.1:c.1162A=	NP_001336797.1:p.Asn388=
NM_001349869.1:c.1144A=	NP_001336798.1:p.Asn382=
NM_003560.3:c.1840A=	NP_003551.2:p.Asn614=
XM_005261764.3:c.1840A=	XP_005261821.1:p.Asn614=
XM_005261765.2:c.1840A=	XP_005261822.1:p.Asn614=
XM_006724332.4:c.1840A=	XP_006724395.1:p.Asn614=
XM_017028983.1:c.1144A=	XP_016884472.1:p.Asn382=
XM_024452280.1:c.1306A=	XP_024308048.1:p.Asn436=
XM_024452281.1:c.1306A=	XP_024308049.1:p.Asn436=
XM_024452282.1:c.1306A=	XP_024308050.1:p.Asn436=
XM_024452283.1:c.1162A=	XP_024308051.1:p.Asn388=
XM_024452284.1:c.1144A=	XP_024308052.1:p.Asn382=
XM_024452285.1:c.1144A=	XP_024308053.1:p.Asn382=
XR_001755325.2:n.2023A=
XR_001755327.2:n.2018A=
XR_001755328.2:n.1984A=
XR_244390.3:n.1932A=
XR_937938.3:n.2018A=
XR_937939.3:n.2075A=
NM_001199562.3:c.1678A=	NP_001186491.1:p.Asn560=
NM_001349864.2:c.1840A=	NP_001336793.1:p.Asn614=
NM_001349865.2:c.1678A=	NP_001336794.1:p.Asn560=
NM_001349866.2:c.1678A=	NP_001336795.1:p.Asn560=
NM_001349867.2:c.1306A=	NP_001336796.1:p.Asn436=
NM_001349868.2:c.1162A=	NP_001336797.1:p.Asn388=
NM_001349869.2:c.1144A=	NP_001336798.1:p.Asn382=
NM_003560.4:c.1840A= MANE Select	NP_003551.2:p.Asn614=
NM_001004426.3:c.1678A=	NP_001004426.1:p.Asn560=