Canonical Allele Identifier: CA2404669663
Gene: PLA2G6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38116120G= , CM000684.2:g.38116120G= GRCh38
NC_000022.10:g.38512127G= , CM000684.1:g.38512127G= GRCh37
NC_000022.9:g.36842073G= NCBI36
NG_007094.2:g.94571C=
NG_007094.3:g.103659C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332509.8:c.1834C= MANE Select ENSP00000333142.3:p.Arg612=
ENST00000427114.6:c.1138C= ENSP00000407743.2:p.Arg380=
ENST00000436218.6:c.*1032C= ENSP00000401242.1:n.*1032C=
ENST00000655142.1:c.*692C= ENSP00000499715.1:n.*692C=
ENST00000660610.1:c.1834C= ENSP00000499555.1:p.Arg612=
ENST00000663895.1:c.1834C= ENSP00000499712.1:p.Arg612=
ENST00000664587.1:c.1696C= ENSP00000499394.1:p.Arg566=
ENST00000665987.1:c.*1573C= ENSP00000499423.1:n.*1573C=
ENST00000667521.1:c.1834C= ENSP00000499665.1:p.Arg612=
ENST00000668499.1:c.*1556C= ENSP00000499626.1:n.*1556C=
ENST00000668949.1:c.1672C= ENSP00000499711.1:p.Arg558=
ENST00000671093.1:n.1766C=
ENST00000673413.1:c.*1503C= ENSP00000500600.1:n.*1503C=
ENST00000332509.7:c.1834C= ENSP00000333142.3:p.Arg612=
ENST00000335539.7:c.1672C= ENSP00000335149.3:p.Arg558=
ENST00000402064.5:c.1672C= ENSP00000386100.1:p.Arg558=
ENST00000448094.5:c.*439C= ENSP00000407106.1:n.*439C=
ENST00000454670.1:c.570C=
ENST00000496409.1:n.374C=
NM_001004426.1:c.1672C= NP_001004426.1:p.Arg558=
NM_001199562.1:c.1672C= NP_001186491.1:p.Arg558=
NM_003560.2:c.1834C= NP_003551.2:p.Arg612=
XM_005261764.1:c.1834C= XP_005261821.1:p.Arg612=
XM_005261765.1:c.1834C= XP_005261822.1:p.Arg612=
XM_005261766.1:c.1834C= XP_005261823.1:p.Arg612=
XM_006724332.2:c.1834C= XP_006724395.1:p.Arg612=
XM_011530422.1:c.1729C= XP_011528724.1:p.Arg577=
XM_011530423.1:c.1300C= XP_011528725.1:p.Arg434=
XM_011530424.1:c.1300C= XP_011528726.1:p.Arg434=
XM_011530425.1:c.1300C= XP_011528727.1:p.Arg434=
XR_244390.1:n.1942C=
XR_430411.1:n.1994C=
XR_937937.1:n.2033C=
XR_937938.1:n.2028C=
XR_937939.1:n.2085C=
NM_001004426.2:c.1672C= NP_001004426.1:p.Arg558=
NM_001199562.2:c.1672C= NP_001186491.1:p.Arg558=
NM_001349864.1:c.1834C= NP_001336793.1:p.Arg612=
NM_001349865.1:c.1672C= NP_001336794.1:p.Arg558=
NM_001349866.1:c.1672C= NP_001336795.1:p.Arg558=
NM_001349867.1:c.1300C= NP_001336796.1:p.Arg434=
NM_001349868.1:c.1156C= NP_001336797.1:p.Arg386=
NM_001349869.1:c.1138C= NP_001336798.1:p.Arg380=
NM_003560.3:c.1834C= NP_003551.2:p.Arg612=
XM_005261764.3:c.1834C= XP_005261821.1:p.Arg612=
XM_005261765.2:c.1834C= XP_005261822.1:p.Arg612=
XM_006724332.4:c.1834C= XP_006724395.1:p.Arg612=
XM_017028983.1:c.1138C= XP_016884472.1:p.Arg380=
XM_024452280.1:c.1300C= XP_024308048.1:p.Arg434=
XM_024452281.1:c.1300C= XP_024308049.1:p.Arg434=
XM_024452282.1:c.1300C= XP_024308050.1:p.Arg434=
XM_024452283.1:c.1156C= XP_024308051.1:p.Arg386=
XM_024452284.1:c.1138C= XP_024308052.1:p.Arg380=
XM_024452285.1:c.1138C= XP_024308053.1:p.Arg380=
XR_001755325.2:n.2017C=
XR_001755327.2:n.2012C=
XR_001755328.2:n.1978C=
XR_244390.3:n.1926C=
XR_937938.3:n.2012C=
XR_937939.3:n.2069C=
NM_001199562.3:c.1672C= NP_001186491.1:p.Arg558=
NM_001349864.2:c.1834C= NP_001336793.1:p.Arg612=
NM_001349865.2:c.1672C= NP_001336794.1:p.Arg558=
NM_001349866.2:c.1672C= NP_001336795.1:p.Arg558=
NM_001349867.2:c.1300C= NP_001336796.1:p.Arg434=
NM_001349868.2:c.1156C= NP_001336797.1:p.Arg386=
NM_001349869.2:c.1138C= NP_001336798.1:p.Arg380=
NM_003560.4:c.1834C= MANE Select NP_003551.2:p.Arg612=
NM_001004426.3:c.1672C= NP_001004426.1:p.Arg558=