Canonical Allele Identifier: CA2656643163

Gene: PLA2G6

Linked Data

• gnomAD v4: 22-38123007-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38123011_38123012del , CM000684.2:g.38123011_38123012del	GRCh38
NC_000022.10:g.38519018_38519019del , CM000684.1:g.38519018_38519019del	GRCh37
NC_000022.9:g.36848964_36848965del	NCBI36
NG_007094.2:g.87682_87683del
NG_007094.3:g.96770_96771del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1591+86_1591+87del MANE Select	ENSP00000333142.3:n.1591+86_1591+87del
ENST00000427114.6:c.895+86_895+87del	ENSP00000407743.2:n.895+86_895+87del
ENST00000436218.6:c.*789+86_*789+87del	ENSP00000401242.1:n.*789+86_*789+87del
ENST00000655142.1:c.*449+86_*449+87del	ENSP00000499715.1:n.*449+86_*449+87del
ENST00000660610.1:c.1591+86_1591+87del	ENSP00000499555.1:n.1591+86_1591+87del
ENST00000663895.1:c.1591+86_1591+87del	ENSP00000499712.1:n.1591+86_1591+87del
ENST00000664587.1:c.1453+86_1453+87del	ENSP00000499394.1:n.1453+86_1453+87del
ENST00000665987.1:c.*1330+86_*1330+87del	ENSP00000499423.1:n.*1330+86_*1330+87del
ENST00000667521.1:c.1591+86_1591+87del	ENSP00000499665.1:n.1591+86_1591+87del
ENST00000668208.1:n.1559+86_1559+87del
ENST00000668499.1:c.*1313+86_*1313+87del	ENSP00000499626.1:n.*1313+86_*1313+87del
ENST00000668949.1:c.1429+86_1429+87del	ENSP00000499711.1:n.1429+86_1429+87del
ENST00000671093.1:n.1523+86_1523+87del
ENST00000673413.1:c.*1260+86_*1260+87del	ENSP00000500600.1:n.*1260+86_*1260+87del
ENST00000332509.7:c.1591+86_1591+87del	ENSP00000333142.3:n.1591+86_1591+87del
ENST00000335539.7:c.1429+86_1429+87del	ENSP00000335149.3:n.1429+86_1429+87del
ENST00000402064.5:c.1429+86_1429+87del	ENSP00000386100.1:n.1429+86_1429+87del
ENST00000448094.5:c.*196+86_*196+87del	ENSP00000407106.1:n.*196+86_*196+87del
ENST00000454670.1:c.236+86_236+87del
ENST00000491986.1:n.602+86_602+87del
NM_001004426.1:c.1429+86_1429+87del	NP_001004426.1:n.1429+86_1429+87del
NM_001199562.1:c.1429+86_1429+87del	NP_001186491.1:n.1429+86_1429+87del
NM_003560.2:c.1591+86_1591+87del	NP_003551.2:n.1591+86_1591+87del
XM_005261764.1:c.1591+86_1591+87del	XP_005261821.1:n.1591+86_1591+87del
XM_005261765.1:c.1591+86_1591+87del	XP_005261822.1:n.1591+86_1591+87del
XM_005261766.1:c.1591+86_1591+87del	XP_005261823.1:n.1591+86_1591+87del
XM_006724332.2:c.1591+86_1591+87del	XP_006724395.1:n.1591+86_1591+87del
XM_011530422.1:c.1486+86_1486+87del	XP_011528724.1:n.1486+86_1486+87del
XM_011530423.1:c.1057+86_1057+87del	XP_011528725.1:n.1057+86_1057+87del
XM_011530424.1:c.1057+86_1057+87del	XP_011528726.1:n.1057+86_1057+87del
XM_011530425.1:c.1057+86_1057+87del	XP_011528727.1:n.1057+86_1057+87del
XM_011530426.1:c.1591+86_1591+87del	XP_011528728.1:n.1591+86_1591+87del
XR_244390.1:n.1699+86_1699+87del
XR_244392.1:n.1752+86_1752+87del
XR_430411.1:n.1751+86_1751+87del
XR_430412.1:n.1804+86_1804+87del
XR_937937.1:n.1699+86_1699+87del
XR_937938.1:n.1699+86_1699+87del
XR_937939.1:n.1751+86_1751+87del
XR_937940.1:n.1751+86_1751+87del
NM_001004426.2:c.1429+86_1429+87del	NP_001004426.1:n.1429+86_1429+87del
NM_001199562.2:c.1429+86_1429+87del	NP_001186491.1:n.1429+86_1429+87del
NM_001349864.1:c.1591+86_1591+87del	NP_001336793.1:n.1591+86_1591+87del
NM_001349865.1:c.1429+86_1429+87del	NP_001336794.1:n.1429+86_1429+87del
NM_001349866.1:c.1429+86_1429+87del	NP_001336795.1:n.1429+86_1429+87del
NM_001349867.1:c.1057+86_1057+87del	NP_001336796.1:n.1057+86_1057+87del
NM_001349868.1:c.913+86_913+87del	NP_001336797.1:n.913+86_913+87del
NM_001349869.1:c.895+86_895+87del	NP_001336798.1:n.895+86_895+87del
NM_003560.3:c.1591+86_1591+87del	NP_003551.2:n.1591+86_1591+87del
XM_005261764.3:c.1591+86_1591+87del	XP_005261821.1:n.1591+86_1591+87del
XM_005261765.2:c.1591+86_1591+87del	XP_005261822.1:n.1591+86_1591+87del
XM_006724332.4:c.1591+86_1591+87del	XP_006724395.1:n.1591+86_1591+87del
XM_011530426.3:c.1591+86_1591+87del	XP_011528728.1:n.1591+86_1591+87del
XM_017028983.1:c.895+86_895+87del	XP_016884472.1:n.895+86_895+87del
XM_017028986.2:c.1429+86_1429+87del	XP_016884475.1:n.1429+86_1429+87del
XM_024452280.1:c.1057+86_1057+87del	XP_024308048.1:n.1057+86_1057+87del
XM_024452281.1:c.1057+86_1057+87del	XP_024308049.1:n.1057+86_1057+87del
XM_024452282.1:c.1057+86_1057+87del	XP_024308050.1:n.1057+86_1057+87del
XM_024452283.1:c.913+86_913+87del	XP_024308051.1:n.913+86_913+87del
XM_024452284.1:c.895+86_895+87del	XP_024308052.1:n.895+86_895+87del
XM_024452285.1:c.895+86_895+87del	XP_024308053.1:n.895+86_895+87del
XR_001755325.2:n.1683+86_1683+87del
XR_001755327.2:n.1683+86_1683+87del
XR_001755328.2:n.1735+86_1735+87del
XR_244390.3:n.1683+86_1683+87del
XR_937938.3:n.1683+86_1683+87del
XR_937939.3:n.1735+86_1735+87del
XR_937940.3:n.1735+86_1735+87del
NM_001199562.3:c.1429+86_1429+87del	NP_001186491.1:n.1429+86_1429+87del
NM_001349864.2:c.1591+86_1591+87del	NP_001336793.1:n.1591+86_1591+87del
NM_001349865.2:c.1429+86_1429+87del	NP_001336794.1:n.1429+86_1429+87del
NM_001349866.2:c.1429+86_1429+87del	NP_001336795.1:n.1429+86_1429+87del
NM_001349867.2:c.1057+86_1057+87del	NP_001336796.1:n.1057+86_1057+87del
NM_001349868.2:c.913+86_913+87del	NP_001336797.1:n.913+86_913+87del
NM_001349869.2:c.895+86_895+87del	NP_001336798.1:n.895+86_895+87del
NM_003560.4:c.1591+86_1591+87del MANE Select	NP_003551.2:n.1591+86_1591+87del
NM_001004426.3:c.1429+86_1429+87del	NP_001004426.1:n.1429+86_1429+87del