Canonical Allele Identifier: CA2656637249

Gene: PLA2G6

Linked Data

• gnomAD v4: 22-38113762-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38113763del , CM000684.2:g.38113763del	GRCh38
NC_000022.10:g.38509770del , CM000684.1:g.38509770del	GRCh37
NC_000022.9:g.36839716del	NCBI36
NG_007094.2:g.96928del
NG_033059.2:g.1907del
NG_007094.3:g.106016del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.2035-109del MANE Select	ENSP00000333142.3:n.2035-109del
ENST00000436218.6:c.*1233-109del	ENSP00000401242.1:n.*1233-109del
ENST00000655142.1:c.*893-109del	ENSP00000499715.1:n.*893-109del
ENST00000660610.1:c.2035-109del	ENSP00000499555.1:n.2035-109del
ENST00000663895.1:c.2035-109del	ENSP00000499712.1:n.2035-109del
ENST00000664587.1:c.1897-109del	ENSP00000499394.1:n.1897-109del
ENST00000665987.1:c.*1774-109del	ENSP00000499423.1:n.*1774-109del
ENST00000667521.1:c.2035-109del	ENSP00000499665.1:n.2035-109del
ENST00000668499.1:c.*1894-109del	ENSP00000499626.1:n.*1894-109del
ENST00000668949.1:c.2077-109del	ENSP00000499711.1:n.2077-109del
ENST00000671093.1:n.1967-109del
ENST00000673413.1:c.*1704-109del	ENSP00000500600.1:n.*1704-109del
ENST00000332509.7:c.2035-109del	ENSP00000333142.3:n.2035-109del
ENST00000335539.7:c.1873-109del	ENSP00000335149.3:n.1873-109del
ENST00000402064.5:c.1873-109del	ENSP00000386100.1:n.1873-109del
ENST00000496409.1:n.743-109del
NM_001004426.1:c.1873-109del	NP_001004426.1:n.1873-109del
NM_001199562.1:c.1873-109del	NP_001186491.1:n.1873-109del
NM_003560.2:c.2035-109del	NP_003551.2:n.2035-109del
XM_005261764.1:c.2035-109del	XP_005261821.1:n.2035-109del
XM_005261765.1:c.2035-109del	XP_005261822.1:n.2035-109del
XM_005261766.1:c.2035-109del	XP_005261823.1:n.2035-109del
XM_006724332.2:c.2035-109del	XP_006724395.1:n.2035-109del
XM_011530422.1:c.1930-109del	XP_011528724.1:n.1930-109del
XM_011530423.1:c.1501-109del	XP_011528725.1:n.1501-109del
XM_011530424.1:c.1501-109del	XP_011528726.1:n.1501-109del
XM_011530425.1:c.1501-109del	XP_011528727.1:n.1501-109del
XR_244390.1:n.2311-109del
XR_430411.1:n.2195-109del
XR_937938.1:n.2397-109del
NM_001004426.2:c.1873-109del	NP_001004426.1:n.1873-109del
NM_001199562.2:c.1873-109del	NP_001186491.1:n.1873-109del
NM_001349864.1:c.2035-109del	NP_001336793.1:n.2035-109del
NM_001349865.1:c.1873-109del	NP_001336794.1:n.1873-109del
NM_001349866.1:c.1873-109del	NP_001336795.1:n.1873-109del
NM_001349867.1:c.1501-109del	NP_001336796.1:n.1501-109del
NM_001349868.1:c.1357-109del	NP_001336797.1:n.1357-109del
NM_001349869.1:c.1339-109del	NP_001336798.1:n.1339-109del
NM_003560.3:c.2035-109del	NP_003551.2:n.2035-109del
XM_005261764.3:c.2035-109del	XP_005261821.1:n.2035-109del
XM_005261765.2:c.2035-109del	XP_005261822.1:n.2035-109del
XM_006724332.4:c.2035-109del	XP_006724395.1:n.2035-109del
XM_017028983.1:c.1339-109del	XP_016884472.1:n.1339-109del
XM_024452280.1:c.1501-109del	XP_024308048.1:n.1501-109del
XM_024452281.1:c.1501-109del	XP_024308049.1:n.1501-109del
XM_024452282.1:c.1501-109del	XP_024308050.1:n.1501-109del
XM_024452283.1:c.1357-109del	XP_024308051.1:n.1357-109del
XM_024452284.1:c.1339-109del	XP_024308052.1:n.1339-109del
XM_024452285.1:c.1339-109del	XP_024308053.1:n.1339-109del
XR_001755325.2:n.2218-109del
XR_001755327.2:n.2213-109del
XR_001755328.2:n.2179-109del
XR_244390.3:n.2295-109del
XR_937938.3:n.2381-109del
NM_001199562.3:c.1873-109del	NP_001186491.1:n.1873-109del
NM_001349864.2:c.2035-109del	NP_001336793.1:n.2035-109del
NM_001349865.2:c.1873-109del	NP_001336794.1:n.1873-109del
NM_001349866.2:c.1873-109del	NP_001336795.1:n.1873-109del
NM_001349867.2:c.1501-109del	NP_001336796.1:n.1501-109del
NM_001349868.2:c.1357-109del	NP_001336797.1:n.1357-109del
NM_001349869.2:c.1339-109del	NP_001336798.1:n.1339-109del
NM_003560.4:c.2035-109del MANE Select	NP_003551.2:n.2035-109del
NM_001004426.3:c.1873-109del	NP_001004426.1:n.1873-109del