Canonical Allele Identifier: CA639216157

Gene: PLA2G6

Linked Data

• dbSNP Id: rs1291131519
• gnomAD v2: 22-38516499-C-CGGCAGGGCAGAGCCG
• gnomAD v3: 22-38120492-C-CGGCAGGGCAGAGCCG
• gnomAD v4: 22-38120492-C-CGGCAGGGCAGAGCCG
• MyVariant Identifiers: chr22:g.38516529delinsGGGCAGGGCAGAGCCA (hg19) ; chr22:g.38120522delinsGGGCAGGGCAGAGCCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38120507_38120521dup , CM000684.2:g.38120507_38120521dup	GRCh38
NC_000022.10:g.38516514_38516528dup , CM000684.1:g.38516514_38516528dup	GRCh37
NC_000022.9:g.36846460_36846474dup	NCBI36
NG_007094.2:g.90184_90198dup
NG_007094.3:g.99272_99286dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1742+252_1742+266dup MANE Select	ENSP00000333142.3:n.1742+252_1742+266dup
ENST00000427114.6:c.1046+252_1046+266dup	ENSP00000407743.2:n.1046+252_1046+266dup
ENST00000436218.6:c.*940+252_*940+266dup	ENSP00000401242.1:n.*940+252_*940+266dup
ENST00000655142.1:c.*600+252_*600+266dup	ENSP00000499715.1:n.*600+252_*600+266dup
ENST00000660610.1:c.1742+252_1742+266dup	ENSP00000499555.1:n.1742+252_1742+266dup
ENST00000663895.1:c.1742+252_1742+266dup	ENSP00000499712.1:n.1742+252_1742+266dup
ENST00000664587.1:c.1604+252_1604+266dup	ENSP00000499394.1:n.1604+252_1604+266dup
ENST00000665987.1:c.*1481+252_*1481+266dup	ENSP00000499423.1:n.*1481+252_*1481+266dup
ENST00000667521.1:c.1742+252_1742+266dup	ENSP00000499665.1:n.1742+252_1742+266dup
ENST00000668208.1:n.1710+252_1710+266dup
ENST00000668499.1:c.*1464+252_*1464+266dup	ENSP00000499626.1:n.*1464+252_*1464+266dup
ENST00000668949.1:c.1580+252_1580+266dup	ENSP00000499711.1:n.1580+252_1580+266dup
ENST00000671093.1:n.1674+252_1674+266dup
ENST00000673413.1:c.*1411+252_*1411+266dup	ENSP00000500600.1:n.*1411+252_*1411+266dup
ENST00000332509.7:c.1742+252_1742+266dup	ENSP00000333142.3:n.1742+252_1742+266dup
ENST00000335539.7:c.1580+252_1580+266dup	ENSP00000335149.3:n.1580+252_1580+266dup
ENST00000402064.5:c.1580+252_1580+266dup	ENSP00000386100.1:n.1580+252_1580+266dup
ENST00000448094.5:c.*347+252_*347+266dup	ENSP00000407106.1:n.*347+252_*347+266dup
ENST00000454670.1:c.387+252_387+266dup
ENST00000496409.1:n.282+252_282+266dup
NM_001004426.1:c.1580+252_1580+266dup	NP_001004426.1:n.1580+252_1580+266dup
NM_001199562.1:c.1580+252_1580+266dup	NP_001186491.1:n.1580+252_1580+266dup
NM_003560.2:c.1742+252_1742+266dup	NP_003551.2:n.1742+252_1742+266dup
XM_005261764.1:c.1742+252_1742+266dup	XP_005261821.1:n.1742+252_1742+266dup
XM_005261765.1:c.1742+252_1742+266dup	XP_005261822.1:n.1742+252_1742+266dup
XM_005261766.1:c.1742+252_1742+266dup	XP_005261823.1:n.1742+252_1742+266dup
XM_006724332.2:c.1742+252_1742+266dup	XP_006724395.1:n.1742+252_1742+266dup
XM_011530422.1:c.1637+252_1637+266dup	XP_011528724.1:n.1637+252_1637+266dup
XM_011530423.1:c.1208+252_1208+266dup	XP_011528725.1:n.1208+252_1208+266dup
XM_011530424.1:c.1208+252_1208+266dup	XP_011528726.1:n.1208+252_1208+266dup
XM_011530425.1:c.1208+252_1208+266dup	XP_011528727.1:n.1208+252_1208+266dup
XM_011530426.1:c.1742+252_1742+266dup	XP_011528728.1:n.1742+252_1742+266dup
XR_244390.1:n.1850+252_1850+266dup
XR_430411.1:n.1902+252_1902+266dup
XR_937937.1:n.1850+252_1850+266dup
XR_937938.1:n.1936+252_1936+266dup
XR_937939.1:n.1902+252_1902+266dup
NM_001004426.2:c.1580+252_1580+266dup	NP_001004426.1:n.1580+252_1580+266dup
NM_001199562.2:c.1580+252_1580+266dup	NP_001186491.1:n.1580+252_1580+266dup
NM_001349864.1:c.1742+252_1742+266dup	NP_001336793.1:n.1742+252_1742+266dup
NM_001349865.1:c.1580+252_1580+266dup	NP_001336794.1:n.1580+252_1580+266dup
NM_001349866.1:c.1580+252_1580+266dup	NP_001336795.1:n.1580+252_1580+266dup
NM_001349867.1:c.1208+252_1208+266dup	NP_001336796.1:n.1208+252_1208+266dup
NM_001349868.1:c.1064+252_1064+266dup	NP_001336797.1:n.1064+252_1064+266dup
NM_001349869.1:c.1046+252_1046+266dup	NP_001336798.1:n.1046+252_1046+266dup
NM_003560.3:c.1742+252_1742+266dup	NP_003551.2:n.1742+252_1742+266dup
XM_005261764.3:c.1742+252_1742+266dup	XP_005261821.1:n.1742+252_1742+266dup
XM_005261765.2:c.1742+252_1742+266dup	XP_005261822.1:n.1742+252_1742+266dup
XM_006724332.4:c.1742+252_1742+266dup	XP_006724395.1:n.1742+252_1742+266dup
XM_011530426.3:c.1742+252_1742+266dup	XP_011528728.1:n.1742+252_1742+266dup
XM_017028983.1:c.1046+252_1046+266dup	XP_016884472.1:n.1046+252_1046+266dup
XM_017028986.2:c.1580+252_1580+266dup	XP_016884475.1:n.1580+252_1580+266dup
XM_024452280.1:c.1208+252_1208+266dup	XP_024308048.1:n.1208+252_1208+266dup
XM_024452281.1:c.1208+252_1208+266dup	XP_024308049.1:n.1208+252_1208+266dup
XM_024452282.1:c.1208+252_1208+266dup	XP_024308050.1:n.1208+252_1208+266dup
XM_024452283.1:c.1064+252_1064+266dup	XP_024308051.1:n.1064+252_1064+266dup
XM_024452284.1:c.1046+252_1046+266dup	XP_024308052.1:n.1046+252_1046+266dup
XM_024452285.1:c.1046+252_1046+266dup	XP_024308053.1:n.1046+252_1046+266dup
XR_001755325.2:n.1834+252_1834+266dup
XR_001755327.2:n.1920+252_1920+266dup
XR_001755328.2:n.1886+252_1886+266dup
XR_244390.3:n.1834+252_1834+266dup
XR_937938.3:n.1920+252_1920+266dup
XR_937939.3:n.1886+252_1886+266dup
NM_001199562.3:c.1580+252_1580+266dup	NP_001186491.1:n.1580+252_1580+266dup
NM_001349864.2:c.1742+252_1742+266dup	NP_001336793.1:n.1742+252_1742+266dup
NM_001349865.2:c.1580+252_1580+266dup	NP_001336794.1:n.1580+252_1580+266dup
NM_001349866.2:c.1580+252_1580+266dup	NP_001336795.1:n.1580+252_1580+266dup
NM_001349867.2:c.1208+252_1208+266dup	NP_001336796.1:n.1208+252_1208+266dup
NM_001349868.2:c.1064+252_1064+266dup	NP_001336797.1:n.1064+252_1064+266dup
NM_001349869.2:c.1046+252_1046+266dup	NP_001336798.1:n.1046+252_1046+266dup
NM_003560.4:c.1742+252_1742+266dup MANE Select	NP_003551.2:n.1742+252_1742+266dup
NM_001004426.3:c.1580+252_1580+266dup	NP_001004426.1:n.1580+252_1580+266dup