Canonical Allele Identifier: CA2842038616

Gene: PLA2G6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38116033G>T , CM000684.2:g.38116033G>T	GRCh38
NC_000022.10:g.38512040G>T , CM000684.1:g.38512040G>T	GRCh37
NC_000022.9:g.36841986G>T	NCBI36
NG_007094.2:g.94658C>A
NG_007094.3:g.103746C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1879+42C>A MANE Select	ENSP00000333142.3:n.1879+42C>A
ENST00000427114.6:c.1183+42C>A	ENSP00000407743.2:n.1183+42C>A
ENST00000436218.6:c.*1077+42C>A	ENSP00000401242.1:n.*1077+42C>A
ENST00000655142.1:c.*737+42C>A	ENSP00000499715.1:n.*737+42C>A
ENST00000660610.1:c.1879+42C>A	ENSP00000499555.1:n.1879+42C>A
ENST00000663895.1:c.1879+42C>A	ENSP00000499712.1:n.1879+42C>A
ENST00000664587.1:c.1741+42C>A	ENSP00000499394.1:n.1741+42C>A
ENST00000665987.1:c.*1618+42C>A	ENSP00000499423.1:n.*1618+42C>A
ENST00000667521.1:c.1879+42C>A	ENSP00000499665.1:n.1879+42C>A
ENST00000668499.1:c.*1601+42C>A	ENSP00000499626.1:n.*1601+42C>A
ENST00000668949.1:c.1717+42C>A	ENSP00000499711.1:n.1717+42C>A
ENST00000671093.1:n.1811+42C>A
ENST00000673413.1:c.*1548+42C>A	ENSP00000500600.1:n.*1548+42C>A
ENST00000332509.7:c.1879+42C>A	ENSP00000333142.3:n.1879+42C>A
ENST00000335539.7:c.1717+42C>A	ENSP00000335149.3:n.1717+42C>A
ENST00000402064.5:c.1717+42C>A	ENSP00000386100.1:n.1717+42C>A
ENST00000454670.1:c.615+42C>A
ENST00000496409.1:n.419+42C>A
NM_001004426.1:c.1717+42C>A	NP_001004426.1:n.1717+42C>A
NM_001199562.1:c.1717+42C>A	NP_001186491.1:n.1717+42C>A
NM_003560.2:c.1879+42C>A	NP_003551.2:n.1879+42C>A
XM_005261764.1:c.1879+42C>A	XP_005261821.1:n.1879+42C>A
XM_005261765.1:c.1879+42C>A	XP_005261822.1:n.1879+42C>A
XM_005261766.1:c.1879+42C>A	XP_005261823.1:n.1879+42C>A
XM_006724332.2:c.1879+42C>A	XP_006724395.1:n.1879+42C>A
XM_011530422.1:c.1774+42C>A	XP_011528724.1:n.1774+42C>A
XM_011530423.1:c.1345+42C>A	XP_011528725.1:n.1345+42C>A
XM_011530424.1:c.1345+42C>A	XP_011528726.1:n.1345+42C>A
XM_011530425.1:c.1345+42C>A	XP_011528727.1:n.1345+42C>A
XR_244390.1:n.1987+42C>A
XR_430411.1:n.2039+42C>A
XR_937937.1:n.2078+42C>A
XR_937938.1:n.2073+42C>A
XR_937939.1:n.2130+42C>A
NM_001004426.2:c.1717+42C>A	NP_001004426.1:n.1717+42C>A
NM_001199562.2:c.1717+42C>A	NP_001186491.1:n.1717+42C>A
NM_001349864.1:c.1879+42C>A	NP_001336793.1:n.1879+42C>A
NM_001349865.1:c.1717+42C>A	NP_001336794.1:n.1717+42C>A
NM_001349866.1:c.1717+42C>A	NP_001336795.1:n.1717+42C>A
NM_001349867.1:c.1345+42C>A	NP_001336796.1:n.1345+42C>A
NM_001349868.1:c.1201+42C>A	NP_001336797.1:n.1201+42C>A
NM_001349869.1:c.1183+42C>A	NP_001336798.1:n.1183+42C>A
NM_003560.3:c.1879+42C>A	NP_003551.2:n.1879+42C>A
XM_005261764.3:c.1879+42C>A	XP_005261821.1:n.1879+42C>A
XM_005261765.2:c.1879+42C>A	XP_005261822.1:n.1879+42C>A
XM_006724332.4:c.1879+42C>A	XP_006724395.1:n.1879+42C>A
XM_017028983.1:c.1183+42C>A	XP_016884472.1:n.1183+42C>A
XM_024452280.1:c.1345+42C>A	XP_024308048.1:n.1345+42C>A
XM_024452281.1:c.1345+42C>A	XP_024308049.1:n.1345+42C>A
XM_024452282.1:c.1345+42C>A	XP_024308050.1:n.1345+42C>A
XM_024452283.1:c.1201+42C>A	XP_024308051.1:n.1201+42C>A
XM_024452284.1:c.1183+42C>A	XP_024308052.1:n.1183+42C>A
XM_024452285.1:c.1183+42C>A	XP_024308053.1:n.1183+42C>A
XR_001755325.2:n.2062+42C>A
XR_001755327.2:n.2057+42C>A
XR_001755328.2:n.2023+42C>A
XR_244390.3:n.1971+42C>A
XR_937938.3:n.2057+42C>A
XR_937939.3:n.2114+42C>A
NM_001199562.3:c.1717+42C>A	NP_001186491.1:n.1717+42C>A
NM_001349864.2:c.1879+42C>A	NP_001336793.1:n.1879+42C>A
NM_001349865.2:c.1717+42C>A	NP_001336794.1:n.1717+42C>A
NM_001349866.2:c.1717+42C>A	NP_001336795.1:n.1717+42C>A
NM_001349867.2:c.1345+42C>A	NP_001336796.1:n.1345+42C>A
NM_001349868.2:c.1201+42C>A	NP_001336797.1:n.1201+42C>A
NM_001349869.2:c.1183+42C>A	NP_001336798.1:n.1183+42C>A
NM_003560.4:c.1879+42C>A MANE Select	NP_003551.2:n.1879+42C>A
NM_001004426.3:c.1717+42C>A	NP_001004426.1:n.1717+42C>A