Canonical Allele Identifier: CA2404671832
Gene: PLA2G6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38120836G= , CM000684.2:g.38120836G= GRCh38
NC_000022.10:g.38516843G= , CM000684.1:g.38516843G= GRCh37
NC_000022.9:g.36846789G= NCBI36
NG_007094.2:g.89855C=
NG_007094.3:g.98943C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332509.8:c.1665C= MANE Select ENSP00000333142.3:p.Tyr555=
ENST00000427114.6:c.969C= ENSP00000407743.2:p.Tyr323=
ENST00000436218.6:c.*863C= ENSP00000401242.1:n.*863C=
ENST00000655142.1:c.*523C= ENSP00000499715.1:n.*523C=
ENST00000660610.1:c.1665C= ENSP00000499555.1:p.Tyr555=
ENST00000663895.1:c.1665C= ENSP00000499712.1:p.Tyr555=
ENST00000664587.1:c.1527C= ENSP00000499394.1:p.Tyr509=
ENST00000665987.1:c.*1404C= ENSP00000499423.1:n.*1404C=
ENST00000667521.1:c.1665C= ENSP00000499665.1:p.Tyr555=
ENST00000668208.1:n.1633C=
ENST00000668499.1:c.*1387C= ENSP00000499626.1:n.*1387C=
ENST00000668949.1:c.1503C= ENSP00000499711.1:p.Tyr501=
ENST00000671093.1:n.1597C=
ENST00000673413.1:c.*1334C= ENSP00000500600.1:n.*1334C=
ENST00000332509.7:c.1665C= ENSP00000333142.3:p.Tyr555=
ENST00000335539.7:c.1503C= ENSP00000335149.3:p.Tyr501=
ENST00000402064.5:c.1503C= ENSP00000386100.1:p.Tyr501=
ENST00000448094.5:c.*270C= ENSP00000407106.1:n.*270C=
ENST00000454670.1:c.310C=
ENST00000491986.1:n.676C=
ENST00000496409.1:n.205C=
NM_001004426.1:c.1503C= NP_001004426.1:p.Tyr501=
NM_001199562.1:c.1503C= NP_001186491.1:p.Tyr501=
NM_003560.2:c.1665C= NP_003551.2:p.Tyr555=
XM_005261764.1:c.1665C= XP_005261821.1:p.Tyr555=
XM_005261765.1:c.1665C= XP_005261822.1:p.Tyr555=
XM_005261766.1:c.1665C= XP_005261823.1:p.Tyr555=
XM_006724332.2:c.1665C= XP_006724395.1:p.Tyr555=
XM_011530422.1:c.1560C= XP_011528724.1:p.Tyr520=
XM_011530423.1:c.1131C= XP_011528725.1:p.Tyr377=
XM_011530424.1:c.1131C= XP_011528726.1:p.Tyr377=
XM_011530425.1:c.1131C= XP_011528727.1:p.Tyr377=
XM_011530426.1:c.1665C= XP_011528728.1:p.Tyr555=
XR_244390.1:n.1773C=
XR_430411.1:n.1825C=
XR_937937.1:n.1773C=
XR_937938.1:n.1859C=
XR_937939.1:n.1825C=
NM_001004426.2:c.1503C= NP_001004426.1:p.Tyr501=
NM_001199562.2:c.1503C= NP_001186491.1:p.Tyr501=
NM_001349864.1:c.1665C= NP_001336793.1:p.Tyr555=
NM_001349865.1:c.1503C= NP_001336794.1:p.Tyr501=
NM_001349866.1:c.1503C= NP_001336795.1:p.Tyr501=
NM_001349867.1:c.1131C= NP_001336796.1:p.Tyr377=
NM_001349868.1:c.987C= NP_001336797.1:p.Tyr329=
NM_001349869.1:c.969C= NP_001336798.1:p.Tyr323=
NM_003560.3:c.1665C= NP_003551.2:p.Tyr555=
XM_005261764.3:c.1665C= XP_005261821.1:p.Tyr555=
XM_005261765.2:c.1665C= XP_005261822.1:p.Tyr555=
XM_006724332.4:c.1665C= XP_006724395.1:p.Tyr555=
XM_011530426.3:c.1665C= XP_011528728.1:p.Tyr555=
XM_017028983.1:c.969C= XP_016884472.1:p.Tyr323=
XM_017028986.2:c.1503C= XP_016884475.1:p.Tyr501=
XM_024452280.1:c.1131C= XP_024308048.1:p.Tyr377=
XM_024452281.1:c.1131C= XP_024308049.1:p.Tyr377=
XM_024452282.1:c.1131C= XP_024308050.1:p.Tyr377=
XM_024452283.1:c.987C= XP_024308051.1:p.Tyr329=
XM_024452284.1:c.969C= XP_024308052.1:p.Tyr323=
XM_024452285.1:c.969C= XP_024308053.1:p.Tyr323=
XR_001755325.2:n.1757C=
XR_001755327.2:n.1843C=
XR_001755328.2:n.1809C=
XR_244390.3:n.1757C=
XR_937938.3:n.1843C=
XR_937939.3:n.1809C=
NM_001199562.3:c.1503C= NP_001186491.1:p.Tyr501=
NM_001349864.2:c.1665C= NP_001336793.1:p.Tyr555=
NM_001349865.2:c.1503C= NP_001336794.1:p.Tyr501=
NM_001349866.2:c.1503C= NP_001336795.1:p.Tyr501=
NM_001349867.2:c.1131C= NP_001336796.1:p.Tyr377=
NM_001349868.2:c.987C= NP_001336797.1:p.Tyr329=
NM_001349869.2:c.969C= NP_001336798.1:p.Tyr323=
NM_003560.4:c.1665C= MANE Select NP_003551.2:p.Tyr555=
NM_001004426.3:c.1503C= NP_001004426.1:p.Tyr501=