Canonical Allele Identifier: CA2404669376

Gene: PLA2G6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38115577G= , CM000684.2:g.38115577G=	GRCh38
NC_000022.10:g.38511584G= , CM000684.1:g.38511584G=	GRCh37
NC_000022.9:g.36841530G=	NCBI36
NG_007094.2:g.95114C=
NG_033059.2:g.93C=
NG_007094.3:g.104202C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1984C= MANE Select	ENSP00000333142.3:p.Leu662=
ENST00000427114.6:c.1288C=	ENSP00000407743.2:p.Leu430=
ENST00000436218.6:c.*1182C=	ENSP00000401242.1:n.*1182C=
ENST00000655142.1:c.*842C=	ENSP00000499715.1:n.*842C=
ENST00000660610.1:c.1984C=	ENSP00000499555.1:p.Leu662=
ENST00000663895.1:c.1984C=	ENSP00000499712.1:p.Leu662=
ENST00000664587.1:c.1846C=	ENSP00000499394.1:p.Leu616=
ENST00000665987.1:c.*1723C=	ENSP00000499423.1:n.*1723C=
ENST00000667521.1:c.1984C=	ENSP00000499665.1:p.Leu662=
ENST00000668499.1:c.*1706C=	ENSP00000499626.1:n.*1706C=
ENST00000668949.1:c.1822C=	ENSP00000499711.1:p.Leu608=
ENST00000671093.1:n.1916C=
ENST00000673413.1:c.*1653C=	ENSP00000500600.1:n.*1653C=
ENST00000332509.7:c.1984C=	ENSP00000333142.3:p.Leu662=
ENST00000335539.7:c.1822C=	ENSP00000335149.3:p.Leu608=
ENST00000402064.5:c.1822C=	ENSP00000386100.1:p.Leu608=
ENST00000454670.1:c.720C=
ENST00000496409.1:n.692C=
NM_001004426.1:c.1822C=	NP_001004426.1:p.Leu608=
NM_001199562.1:c.1822C=	NP_001186491.1:p.Leu608=
NM_003560.2:c.1984C=	NP_003551.2:p.Leu662=
XM_005261764.1:c.1984C=	XP_005261821.1:p.Leu662=
XM_005261765.1:c.1984C=	XP_005261822.1:p.Leu662=
XM_005261766.1:c.1984C=	XP_005261823.1:p.Leu662=
XM_006724332.2:c.1984C=	XP_006724395.1:p.Leu662=
XM_011530422.1:c.1879C=	XP_011528724.1:p.Leu627=
XM_011530423.1:c.1450C=	XP_011528725.1:p.Leu484=
XM_011530424.1:c.1450C=	XP_011528726.1:p.Leu484=
XM_011530425.1:c.1450C=	XP_011528727.1:p.Leu484=
XR_244390.1:n.2260C=
XR_430411.1:n.2144C=
XR_937937.1:n.2183C=
XR_937938.1:n.2346C=
XR_937939.1:n.2235C=
NM_001004426.2:c.1822C=	NP_001004426.1:p.Leu608=
NM_001199562.2:c.1822C=	NP_001186491.1:p.Leu608=
NM_001349864.1:c.1984C=	NP_001336793.1:p.Leu662=
NM_001349865.1:c.1822C=	NP_001336794.1:p.Leu608=
NM_001349866.1:c.1822C=	NP_001336795.1:p.Leu608=
NM_001349867.1:c.1450C=	NP_001336796.1:p.Leu484=
NM_001349868.1:c.1306C=	NP_001336797.1:p.Leu436=
NM_001349869.1:c.1288C=	NP_001336798.1:p.Leu430=
NM_003560.3:c.1984C=	NP_003551.2:p.Leu662=
XM_005261764.3:c.1984C=	XP_005261821.1:p.Leu662=
XM_005261765.2:c.1984C=	XP_005261822.1:p.Leu662=
XM_006724332.4:c.1984C=	XP_006724395.1:p.Leu662=
XM_017028983.1:c.1288C=	XP_016884472.1:p.Leu430=
XM_024452280.1:c.1450C=	XP_024308048.1:p.Leu484=
XM_024452281.1:c.1450C=	XP_024308049.1:p.Leu484=
XM_024452282.1:c.1450C=	XP_024308050.1:p.Leu484=
XM_024452283.1:c.1306C=	XP_024308051.1:p.Leu436=
XM_024452284.1:c.1288C=	XP_024308052.1:p.Leu430=
XM_024452285.1:c.1288C=	XP_024308053.1:p.Leu430=
XR_001755325.2:n.2167C=
XR_001755327.2:n.2162C=
XR_001755328.2:n.2128C=
XR_244390.3:n.2244C=
XR_937938.3:n.2330C=
XR_937939.3:n.2219C=
NM_001199562.3:c.1822C=	NP_001186491.1:p.Leu608=
NM_001349864.2:c.1984C=	NP_001336793.1:p.Leu662=
NM_001349865.2:c.1822C=	NP_001336794.1:p.Leu608=
NM_001349866.2:c.1822C=	NP_001336795.1:p.Leu608=
NM_001349867.2:c.1450C=	NP_001336796.1:p.Leu484=
NM_001349868.2:c.1306C=	NP_001336797.1:p.Leu436=
NM_001349869.2:c.1288C=	NP_001336798.1:p.Leu430=
NM_003560.4:c.1984C= MANE Select	NP_003551.2:p.Leu662=
NM_001004426.3:c.1822C=	NP_001004426.1:p.Leu608=