Canonical Allele Identifier: CA411528002
Gene: PLA2G6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38123209T>A , CM000684.2:g.38123209T>A GRCh38
NC_000022.10:g.38519216T>A , CM000684.1:g.38519216T>A GRCh37
NC_000022.9:g.36849162T>A NCBI36
NG_007094.2:g.87482A>T
NG_007094.3:g.96570A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332509.8:c.1477A>T MANE Select ENSP00000333142.3:p.Ile493Phe
ENST00000427114.6:c.781A>T ENSP00000407743.2:p.Ile261Phe
ENST00000436218.6:c.*675A>T ENSP00000401242.1:n.*675A>T
ENST00000655142.1:c.*335A>T ENSP00000499715.1:n.*335A>T
ENST00000660610.1:c.1477A>T ENSP00000499555.1:p.Ile493Phe
ENST00000663895.1:c.1477A>T ENSP00000499712.1:p.Ile493Phe
ENST00000664587.1:c.1339A>T ENSP00000499394.1:p.Ile447Phe
ENST00000665987.1:c.*1216A>T ENSP00000499423.1:n.*1216A>T
ENST00000667521.1:c.1477A>T ENSP00000499665.1:p.Ile493Phe
ENST00000668208.1:n.1445A>T
ENST00000668499.1:c.*1199A>T ENSP00000499626.1:n.*1199A>T
ENST00000668949.1:c.1315A>T ENSP00000499711.1:p.Ile439Phe
ENST00000671093.1:n.1409A>T
ENST00000673413.1:c.*1146A>T ENSP00000500600.1:n.*1146A>T
ENST00000332509.7:c.1477A>T ENSP00000333142.3:p.Ile493Phe
ENST00000335539.7:c.1315A>T ENSP00000335149.3:p.Ile439Phe
ENST00000402064.5:c.1315A>T ENSP00000386100.1:p.Ile439Phe
ENST00000448094.5:c.*82A>T ENSP00000407106.1:n.*82A>T
ENST00000454670.1:c.122A>T
ENST00000490473.1:n.596A>T
ENST00000491986.1:n.488A>T
NM_001004426.1:c.1315A>T NP_001004426.1:p.Ile439Phe
NM_001199562.1:c.1315A>T NP_001186491.1:p.Ile439Phe
NM_003560.2:c.1477A>T NP_003551.2:p.Ile493Phe
XM_005261764.1:c.1477A>T XP_005261821.1:p.Ile493Phe
XM_005261765.1:c.1477A>T XP_005261822.1:p.Ile493Phe
XM_005261766.1:c.1477A>T XP_005261823.1:p.Ile493Phe
XM_006724332.2:c.1477A>T XP_006724395.1:p.Ile493Phe
XM_011530422.1:c.1372A>T XP_011528724.1:p.Ile458Phe
XM_011530423.1:c.943A>T XP_011528725.1:p.Ile315Phe
XM_011530424.1:c.943A>T XP_011528726.1:p.Ile315Phe
XM_011530425.1:c.943A>T XP_011528727.1:p.Ile315Phe
XM_011530426.1:c.1477A>T XP_011528728.1:p.Ile493Phe
XR_244390.1:n.1585A>T
XR_244392.1:n.1638A>T
XR_430411.1:n.1637A>T
XR_430412.1:n.1690A>T
XR_937937.1:n.1585A>T
XR_937938.1:n.1585A>T
XR_937939.1:n.1637A>T
XR_937940.1:n.1637A>T
NM_001004426.2:c.1315A>T NP_001004426.1:p.Ile439Phe
NM_001199562.2:c.1315A>T NP_001186491.1:p.Ile439Phe
NM_001349864.1:c.1477A>T NP_001336793.1:p.Ile493Phe
NM_001349865.1:c.1315A>T NP_001336794.1:p.Ile439Phe
NM_001349866.1:c.1315A>T NP_001336795.1:p.Ile439Phe
NM_001349867.1:c.943A>T NP_001336796.1:p.Ile315Phe
NM_001349868.1:c.799A>T NP_001336797.1:p.Ile267Phe
NM_001349869.1:c.781A>T NP_001336798.1:p.Ile261Phe
NM_003560.3:c.1477A>T NP_003551.2:p.Ile493Phe
XM_005261764.3:c.1477A>T XP_005261821.1:p.Ile493Phe
XM_005261765.2:c.1477A>T XP_005261822.1:p.Ile493Phe
XM_006724332.4:c.1477A>T XP_006724395.1:p.Ile493Phe
XM_011530426.3:c.1477A>T XP_011528728.1:p.Ile493Phe
XM_017028983.1:c.781A>T XP_016884472.1:p.Ile261Phe
XM_017028986.2:c.1315A>T XP_016884475.1:p.Ile439Phe
XM_017028987.2:c.*82A>T XP_016884476.1:n.*82A>T
XM_017028988.2:c.*90A>T XP_016884477.1:n.*90A>T
XM_024452280.1:c.943A>T XP_024308048.1:p.Ile315Phe
XM_024452281.1:c.943A>T XP_024308049.1:p.Ile315Phe
XM_024452282.1:c.943A>T XP_024308050.1:p.Ile315Phe
XM_024452283.1:c.799A>T XP_024308051.1:p.Ile267Phe
XM_024452284.1:c.781A>T XP_024308052.1:p.Ile261Phe
XM_024452285.1:c.781A>T XP_024308053.1:p.Ile261Phe
XR_001755325.2:n.1569A>T
XR_001755327.2:n.1569A>T
XR_001755328.2:n.1621A>T
XR_244390.3:n.1569A>T
XR_937938.3:n.1569A>T
XR_937939.3:n.1621A>T
XR_937940.3:n.1621A>T
NM_001199562.3:c.1315A>T NP_001186491.1:p.Ile439Phe
NM_001349864.2:c.1477A>T NP_001336793.1:p.Ile493Phe
NM_001349865.2:c.1315A>T NP_001336794.1:p.Ile439Phe
NM_001349866.2:c.1315A>T NP_001336795.1:p.Ile439Phe
NM_001349867.2:c.943A>T NP_001336796.1:p.Ile315Phe
NM_001349868.2:c.799A>T NP_001336797.1:p.Ile267Phe
NM_001349869.2:c.781A>T NP_001336798.1:p.Ile261Phe
NM_003560.4:c.1477A>T MANE Select NP_003551.2:p.Ile493Phe
NM_001004426.3:c.1315A>T NP_001004426.1:p.Ile439Phe