Canonical Allele Identifier: CA2404672823
Gene: PLA2G6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38123096G= , CM000684.2:g.38123096G= GRCh38
NC_000022.10:g.38519103G= , CM000684.1:g.38519103G= GRCh37
NC_000022.9:g.36849049G= NCBI36
NG_007094.2:g.87595C=
NG_007094.3:g.96683C=

Transcript Alleles

HGVS Amino-acid change
ENST00000332509.8:c.1590C= MANE Select ENSP00000333142.3:p.His530=
ENST00000427114.6:c.894C= ENSP00000407743.2:p.His298=
ENST00000436218.6:c.*788C= ENSP00000401242.1:n.*788C=
ENST00000655142.1:c.*448C= ENSP00000499715.1:n.*448C=
ENST00000660610.1:c.1590C= ENSP00000499555.1:p.His530=
ENST00000663895.1:c.1590C= ENSP00000499712.1:p.His530=
ENST00000664587.1:c.1452C= ENSP00000499394.1:p.His484=
ENST00000665987.1:c.*1329C= ENSP00000499423.1:n.*1329C=
ENST00000667521.1:c.1590C= ENSP00000499665.1:p.His530=
ENST00000668208.1:n.1558C=
ENST00000668499.1:c.*1312C= ENSP00000499626.1:n.*1312C=
ENST00000668949.1:c.1428C= ENSP00000499711.1:p.His476=
ENST00000671093.1:n.1522C=
ENST00000673413.1:c.*1259C= ENSP00000500600.1:n.*1259C=
ENST00000332509.7:c.1590C= ENSP00000333142.3:p.His530=
ENST00000335539.7:c.1428C= ENSP00000335149.3:p.His476=
ENST00000402064.5:c.1428C= ENSP00000386100.1:p.His476=
ENST00000448094.5:c.*195C= ENSP00000407106.1:n.*195C=
ENST00000454670.1:c.235C=
ENST00000491986.1:n.601C=
NM_001004426.1:c.1428C= NP_001004426.1:p.His476=
NM_001199562.1:c.1428C= NP_001186491.1:p.His476=
NM_003560.2:c.1590C= NP_003551.2:p.His530=
XM_005261764.1:c.1590C= XP_005261821.1:p.His530=
XM_005261765.1:c.1590C= XP_005261822.1:p.His530=
XM_005261766.1:c.1590C= XP_005261823.1:p.His530=
XM_006724332.2:c.1590C= XP_006724395.1:p.His530=
XM_011530422.1:c.1485C= XP_011528724.1:p.His495=
XM_011530423.1:c.1056C= XP_011528725.1:p.His352=
XM_011530424.1:c.1056C= XP_011528726.1:p.His352=
XM_011530425.1:c.1056C= XP_011528727.1:p.His352=
XM_011530426.1:c.1590C= XP_011528728.1:p.His530=
XR_244390.1:n.1698C=
XR_244392.1:n.1751C=
XR_430411.1:n.1750C=
XR_430412.1:n.1803C=
XR_937937.1:n.1698C=
XR_937938.1:n.1698C=
XR_937939.1:n.1750C=
XR_937940.1:n.1750C=
NM_001004426.2:c.1428C= NP_001004426.1:p.His476=
NM_001199562.2:c.1428C= NP_001186491.1:p.His476=
NM_001349864.1:c.1590C= NP_001336793.1:p.His530=
NM_001349865.1:c.1428C= NP_001336794.1:p.His476=
NM_001349866.1:c.1428C= NP_001336795.1:p.His476=
NM_001349867.1:c.1056C= NP_001336796.1:p.His352=
NM_001349868.1:c.912C= NP_001336797.1:p.His304=
NM_001349869.1:c.894C= NP_001336798.1:p.His298=
NM_003560.3:c.1590C= NP_003551.2:p.His530=
XM_005261764.3:c.1590C= XP_005261821.1:p.His530=
XM_005261765.2:c.1590C= XP_005261822.1:p.His530=
XM_006724332.4:c.1590C= XP_006724395.1:p.His530=
XM_011530426.3:c.1590C= XP_011528728.1:p.His530=
XM_017028983.1:c.894C= XP_016884472.1:p.His298=
XM_017028986.2:c.1428C= XP_016884475.1:p.His476=
XM_024452280.1:c.1056C= XP_024308048.1:p.His352=
XM_024452281.1:c.1056C= XP_024308049.1:p.His352=
XM_024452282.1:c.1056C= XP_024308050.1:p.His352=
XM_024452283.1:c.912C= XP_024308051.1:p.His304=
XM_024452284.1:c.894C= XP_024308052.1:p.His298=
XM_024452285.1:c.894C= XP_024308053.1:p.His298=
XR_001755325.2:n.1682C=
XR_001755327.2:n.1682C=
XR_001755328.2:n.1734C=
XR_244390.3:n.1682C=
XR_937938.3:n.1682C=
XR_937939.3:n.1734C=
XR_937940.3:n.1734C=
NM_001199562.3:c.1428C= NP_001186491.1:p.His476=
NM_001349864.2:c.1590C= NP_001336793.1:p.His530=
NM_001349865.2:c.1428C= NP_001336794.1:p.His476=
NM_001349866.2:c.1428C= NP_001336795.1:p.His476=
NM_001349867.2:c.1056C= NP_001336796.1:p.His352=
NM_001349868.2:c.912C= NP_001336797.1:p.His304=
NM_001349869.2:c.894C= NP_001336798.1:p.His298=
NM_003560.4:c.1590C= MANE Select NP_003551.2:p.His530=
NM_001004426.3:c.1428C= NP_001004426.1:p.His476=