Canonical Allele Identifier: CA3244240262
Community Standard Title: NM_003560.4(PLA2G6):c.1351C= (p.Leu451=)
Gene: PLA2G6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38126447G= , CM000684.2:g.38126447G= GRCh38
NC_000022.10:g.38522454G= , CM000684.1:g.38522454G= GRCh37
NC_000022.9:g.36852400G= NCBI36
NG_007094.2:g.84244C=
NG_007094.3:g.93332C=

Transcript Alleles

HGVS Amino-acid Change
NM_003560.4:c.1351C= MANE Select NP_003551.2:p.Leu451=
ENST00000332509.8:c.1351C= MANE Select ENSP00000333142.3:p.Leu451=
NM_001004426.1:c.1189C= NP_001004426.1:p.Leu397=
NM_001004426.2:c.1189C= NP_001004426.1:p.Leu397=
NM_001004426.3:c.1189C= NP_001004426.1:p.Leu397=
NM_001199562.1:c.1189C= NP_001186491.1:p.Leu397=
NM_001199562.2:c.1189C= NP_001186491.1:p.Leu397=
NM_001199562.3:c.1189C= NP_001186491.1:p.Leu397=
NM_001349864.1:c.1351C= NP_001336793.1:p.Leu451=
NM_001349864.2:c.1351C= NP_001336793.1:p.Leu451=
NM_001349865.1:c.1189C= NP_001336794.1:p.Leu397=
NM_001349865.2:c.1189C= NP_001336794.1:p.Leu397=
NM_001349866.1:c.1189C= NP_001336795.1:p.Leu397=
NM_001349866.2:c.1189C= NP_001336795.1:p.Leu397=
NM_001349867.1:c.817C= NP_001336796.1:p.Leu273=
NM_001349867.2:c.817C= NP_001336796.1:p.Leu273=
NM_001349868.1:c.673C= NP_001336797.1:p.Leu225=
NM_001349868.2:c.673C= NP_001336797.1:p.Leu225=
NM_001349869.1:c.655C= NP_001336798.1:p.Leu219=
NM_001349869.2:c.655C= NP_001336798.1:p.Leu219=
NM_003560.2:c.1351C= NP_003551.2:p.Leu451=
NM_003560.3:c.1351C= NP_003551.2:p.Leu451=
ENST00000332509.7:c.1351C= ENSP00000333142.3:p.Leu451=
ENST00000335539.7:c.1189C= ENSP00000335149.3:p.Leu397=
ENST00000402064.5:c.1189C= ENSP00000386100.1:p.Leu397=
ENST00000427114.6:c.655C= ENSP00000407743.2:p.Leu219=
ENST00000436218.6:c.*549C= ENSP00000401242.1:n.*549C=
ENST00000448094.5:c.584C= ENSP00000407106.1:p.Thr195=
ENST00000471636.5:n.493C=
ENST00000490473.1:n.470C=
ENST00000491986.1:n.309C=
ENST00000655142.1:c.*209C= ENSP00000499715.1:n.*209C=
ENST00000660610.1:c.1351C= ENSP00000499555.1:p.Leu451=
ENST00000663895.1:c.1351C= ENSP00000499712.1:p.Leu451=
ENST00000664587.1:c.1213C= ENSP00000499394.1:p.Leu405=
ENST00000665987.1:c.*1090C= ENSP00000499423.1:n.*1090C=
ENST00000667521.1:c.1351C= ENSP00000499665.1:p.Leu451=
ENST00000668208.1:n.1319C=
ENST00000668499.1:c.*1020C= ENSP00000499626.1:n.*1020C=
ENST00000668949.1:c.1189C= ENSP00000499711.1:p.Leu397=
ENST00000671093.1:n.1283C=
ENST00000673413.1:c.*1020C= ENSP00000500600.1:n.*1020C=
XM_005261764.1:c.1351C= XP_005261821.1:p.Leu451=
XM_005261764.3:c.1351C= XP_005261821.1:p.Leu451=
XM_005261765.1:c.1351C= XP_005261822.1:p.Leu451=
XM_005261765.2:c.1351C= XP_005261822.1:p.Leu451=
XM_005261766.1:c.1351C= XP_005261823.1:p.Leu451=
XM_006724332.2:c.1351C= XP_006724395.1:p.Leu451=
XM_006724332.4:c.1351C= XP_006724395.1:p.Leu451=
XM_011530422.1:c.1246C= XP_011528724.1:p.Leu416=
XM_011530423.1:c.817C= XP_011528725.1:p.Leu273=
XM_011530424.1:c.817C= XP_011528726.1:p.Leu273=
XM_011530425.1:c.817C= XP_011528727.1:p.Leu273=
XM_011530426.1:c.1351C= XP_011528728.1:p.Leu451=
XM_011530426.3:c.1351C= XP_011528728.1:p.Leu451=
XM_017028983.1:c.655C= XP_016884472.1:p.Leu219=
XM_017028986.2:c.1189C= XP_016884475.1:p.Leu397=
XM_017028987.2:c.1403C= XP_016884476.1:p.Thr468=
XM_017028988.2:c.1351C= XP_016884477.1:p.Leu451=
XM_024452280.1:c.817C= XP_024308048.1:p.Leu273=
XM_024452281.1:c.817C= XP_024308049.1:p.Leu273=
XM_024452282.1:c.817C= XP_024308050.1:p.Leu273=
XM_024452283.1:c.673C= XP_024308051.1:p.Leu225=
XM_024452284.1:c.655C= XP_024308052.1:p.Leu219=
XM_024452285.1:c.655C= XP_024308053.1:p.Leu219=
XR_001755325.2:n.1443C=
XR_001755327.2:n.1443C=
XR_001755328.2:n.1495C=
XR_244390.1:n.1459C=
XR_244390.3:n.1443C=
XR_244392.1:n.1459C=
XR_430411.1:n.1511C=
XR_430412.1:n.1511C=
XR_937937.1:n.1459C=
XR_937938.1:n.1459C=
XR_937938.3:n.1443C=
XR_937939.1:n.1511C=
XR_937939.3:n.1495C=
XR_937940.1:n.1511C=
XR_937940.3:n.1495C=