Canonical Allele Identifier: CA2404672854

Gene: PLA2G6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38123176_38123177delinsAG , CM000684.2:g.38123176_38123177delinsAG	GRCh38
NC_000022.10:g.38519183_38519184delinsAG , CM000684.1:g.38519183_38519184delinsAG	GRCh37
NC_000022.9:g.36849129_36849130delinsAG	NCBI36
NG_007094.2:g.87514_87515delinsCT
NG_007094.3:g.96602_96603delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1509_1510delinsCT MANE Select	ENSP00000333142.3:p.Ala503=
ENST00000427114.6:c.813_814delinsCT	ENSP00000407743.2:p.Ala271=
ENST00000436218.6:c.*707_*708delinsCT	ENSP00000401242.1:n.*707_*708delinsCT
ENST00000655142.1:c.*367_*368delinsCT	ENSP00000499715.1:n.*367_*368delinsCT
ENST00000660610.1:c.1509_1510delinsCT	ENSP00000499555.1:p.Ala503=
ENST00000663895.1:c.1509_1510delinsCT	ENSP00000499712.1:p.Ala503=
ENST00000664587.1:c.1371_1372delinsCT	ENSP00000499394.1:p.Ala457=
ENST00000665987.1:c.*1248_*1249delinsCT	ENSP00000499423.1:n.*1248_*1249delinsCT
ENST00000667521.1:c.1509_1510delinsCT	ENSP00000499665.1:p.Ala503=
ENST00000668208.1:n.1477_1478delinsCT
ENST00000668499.1:c.*1231_*1232delinsCT	ENSP00000499626.1:n.*1231_*1232delinsCT
ENST00000668949.1:c.1347_1348delinsCT	ENSP00000499711.1:p.Ala449=
ENST00000671093.1:n.1441_1442delinsCT
ENST00000673413.1:c.*1178_*1179delinsCT	ENSP00000500600.1:n.*1178_*1179delinsCT
ENST00000332509.7:c.1509_1510delinsCT	ENSP00000333142.3:p.Ala503=
ENST00000335539.7:c.1347_1348delinsCT	ENSP00000335149.3:p.Ala449=
ENST00000402064.5:c.1347_1348delinsCT	ENSP00000386100.1:p.Ala449=
ENST00000448094.5:c.*114_*115delinsCT	ENSP00000407106.1:n.*114_*115delinsCT
ENST00000454670.1:c.154_155delinsCT
ENST00000491986.1:n.520_521delinsCT
NM_001004426.1:c.1347_1348delinsCT	NP_001004426.1:p.Ala449=
NM_001199562.1:c.1347_1348delinsCT	NP_001186491.1:p.Ala449=
NM_003560.2:c.1509_1510delinsCT	NP_003551.2:p.Ala503=
XM_005261764.1:c.1509_1510delinsCT	XP_005261821.1:p.Ala503=
XM_005261765.1:c.1509_1510delinsCT	XP_005261822.1:p.Ala503=
XM_005261766.1:c.1509_1510delinsCT	XP_005261823.1:p.Ala503=
XM_006724332.2:c.1509_1510delinsCT	XP_006724395.1:p.Ala503=
XM_011530422.1:c.1404_1405delinsCT	XP_011528724.1:p.Ala468=
XM_011530423.1:c.975_976delinsCT	XP_011528725.1:p.Ala325=
XM_011530424.1:c.975_976delinsCT	XP_011528726.1:p.Ala325=
XM_011530425.1:c.975_976delinsCT	XP_011528727.1:p.Ala325=
XM_011530426.1:c.1509_1510delinsCT	XP_011528728.1:p.Ala503=
XR_244390.1:n.1617_1618delinsCT
XR_244392.1:n.1670_1671delinsCT
XR_430411.1:n.1669_1670delinsCT
XR_430412.1:n.1722_1723delinsCT
XR_937937.1:n.1617_1618delinsCT
XR_937938.1:n.1617_1618delinsCT
XR_937939.1:n.1669_1670delinsCT
XR_937940.1:n.1669_1670delinsCT
NM_001004426.2:c.1347_1348delinsCT	NP_001004426.1:p.Ala449=
NM_001199562.2:c.1347_1348delinsCT	NP_001186491.1:p.Ala449=
NM_001349864.1:c.1509_1510delinsCT	NP_001336793.1:p.Ala503=
NM_001349865.1:c.1347_1348delinsCT	NP_001336794.1:p.Ala449=
NM_001349866.1:c.1347_1348delinsCT	NP_001336795.1:p.Ala449=
NM_001349867.1:c.975_976delinsCT	NP_001336796.1:p.Ala325=
NM_001349868.1:c.831_832delinsCT	NP_001336797.1:p.Ala277=
NM_001349869.1:c.813_814delinsCT	NP_001336798.1:p.Ala271=
NM_003560.3:c.1509_1510delinsCT	NP_003551.2:p.Ala503=
XM_005261764.3:c.1509_1510delinsCT	XP_005261821.1:p.Ala503=
XM_005261765.2:c.1509_1510delinsCT	XP_005261822.1:p.Ala503=
XM_006724332.4:c.1509_1510delinsCT	XP_006724395.1:p.Ala503=
XM_011530426.3:c.1509_1510delinsCT	XP_011528728.1:p.Ala503=
XM_017028983.1:c.813_814delinsCT	XP_016884472.1:p.Ala271=
XM_017028986.2:c.1347_1348delinsCT	XP_016884475.1:p.Ala449=
XM_017028987.2:c.*114_*115delinsCT	XP_016884476.1:n.*114_*115delinsCT
XM_017028988.2:c.*122_*123delinsCT	XP_016884477.1:n.*122_*123delinsCT
XM_024452280.1:c.975_976delinsCT	XP_024308048.1:p.Ala325=
XM_024452281.1:c.975_976delinsCT	XP_024308049.1:p.Ala325=
XM_024452282.1:c.975_976delinsCT	XP_024308050.1:p.Ala325=
XM_024452283.1:c.831_832delinsCT	XP_024308051.1:p.Ala277=
XM_024452284.1:c.813_814delinsCT	XP_024308052.1:p.Ala271=
XM_024452285.1:c.813_814delinsCT	XP_024308053.1:p.Ala271=
XR_001755325.2:n.1601_1602delinsCT
XR_001755327.2:n.1601_1602delinsCT
XR_001755328.2:n.1653_1654delinsCT
XR_244390.3:n.1601_1602delinsCT
XR_937938.3:n.1601_1602delinsCT
XR_937939.3:n.1653_1654delinsCT
XR_937940.3:n.1653_1654delinsCT
NM_001199562.3:c.1347_1348delinsCT	NP_001186491.1:p.Ala449=
NM_001349864.2:c.1509_1510delinsCT	NP_001336793.1:p.Ala503=
NM_001349865.2:c.1347_1348delinsCT	NP_001336794.1:p.Ala449=
NM_001349866.2:c.1347_1348delinsCT	NP_001336795.1:p.Ala449=
NM_001349867.2:c.975_976delinsCT	NP_001336796.1:p.Ala325=
NM_001349868.2:c.831_832delinsCT	NP_001336797.1:p.Ala277=
NM_001349869.2:c.813_814delinsCT	NP_001336798.1:p.Ala271=
NM_003560.4:c.1509_1510delinsCT MANE Select	NP_003551.2:p.Ala503=
NM_001004426.3:c.1347_1348delinsCT	NP_001004426.1:p.Ala449=