Canonical Allele Identifier: CA639216146

Gene: PLA2G6

Linked Data

• dbSNP Id: rs1157247507
• gnomAD v2: 22-38516466-GGCCGGGCAGGGCAGAGCCAGGCAGGGCAGAGCCGGCAGGGCAGA-G
• gnomAD v3: 22-38120459-GGCCGGGCAGGGCAGAGCCAGGCAGGGCAGAGCCGGCAGGGCAGA-G
• gnomAD v4: 22-38120459-GGCCGGGCAGGGCAGAGCCAGGCAGGGCAGAGCCGGCAGGGCAGA-G
• MyVariant Identifiers: chr22:g.38516467_38516510del (hg19) ; chr22:g.38120460_38120503del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38120493_38120536del , CM000684.2:g.38120493_38120536del	GRCh38
NC_000022.10:g.38516500_38516543del , CM000684.1:g.38516500_38516543del	GRCh37
NC_000022.9:g.36846446_36846489del	NCBI36
NG_007094.2:g.90188_90231del
NG_007094.3:g.99276_99319del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1742+256_1742+299del MANE Select	ENSP00000333142.3:n.1742+256_1742+299del
ENST00000427114.6:c.1046+256_1046+299del	ENSP00000407743.2:n.1046+256_1046+299del
ENST00000436218.6:c.*940+256_*940+299del	ENSP00000401242.1:n.*940+256_*940+299del
ENST00000655142.1:c.*600+256_*600+299del	ENSP00000499715.1:n.*600+256_*600+299del
ENST00000660610.1:c.1742+256_1742+299del	ENSP00000499555.1:n.1742+256_1742+299del
ENST00000663895.1:c.1742+256_1742+299del	ENSP00000499712.1:n.1742+256_1742+299del
ENST00000664587.1:c.1604+256_1604+299del	ENSP00000499394.1:n.1604+256_1604+299del
ENST00000665987.1:c.*1481+256_*1481+299del	ENSP00000499423.1:n.*1481+256_*1481+299del
ENST00000667521.1:c.1742+256_1742+299del	ENSP00000499665.1:n.1742+256_1742+299del
ENST00000668208.1:n.1710+256_1710+299del
ENST00000668499.1:c.*1464+256_*1464+299del	ENSP00000499626.1:n.*1464+256_*1464+299del
ENST00000668949.1:c.1580+256_1580+299del	ENSP00000499711.1:n.1580+256_1580+299del
ENST00000671093.1:n.1674+256_1674+299del
ENST00000673413.1:c.*1411+256_*1411+299del	ENSP00000500600.1:n.*1411+256_*1411+299del
ENST00000332509.7:c.1742+256_1742+299del	ENSP00000333142.3:n.1742+256_1742+299del
ENST00000335539.7:c.1580+256_1580+299del	ENSP00000335149.3:n.1580+256_1580+299del
ENST00000402064.5:c.1580+256_1580+299del	ENSP00000386100.1:n.1580+256_1580+299del
ENST00000448094.5:c.*347+256_*347+299del	ENSP00000407106.1:n.*347+256_*347+299del
ENST00000454670.1:c.387+256_387+299del
ENST00000496409.1:n.282+256_282+299del
NM_001004426.1:c.1580+256_1580+299del	NP_001004426.1:n.1580+256_1580+299del
NM_001199562.1:c.1580+256_1580+299del	NP_001186491.1:n.1580+256_1580+299del
NM_003560.2:c.1742+256_1742+299del	NP_003551.2:n.1742+256_1742+299del
XM_005261764.1:c.1742+256_1742+299del	XP_005261821.1:n.1742+256_1742+299del
XM_005261765.1:c.1742+256_1742+299del	XP_005261822.1:n.1742+256_1742+299del
XM_005261766.1:c.1742+256_1742+299del	XP_005261823.1:n.1742+256_1742+299del
XM_006724332.2:c.1742+256_1742+299del	XP_006724395.1:n.1742+256_1742+299del
XM_011530422.1:c.1637+256_1637+299del	XP_011528724.1:n.1637+256_1637+299del
XM_011530423.1:c.1208+256_1208+299del	XP_011528725.1:n.1208+256_1208+299del
XM_011530424.1:c.1208+256_1208+299del	XP_011528726.1:n.1208+256_1208+299del
XM_011530425.1:c.1208+256_1208+299del	XP_011528727.1:n.1208+256_1208+299del
XM_011530426.1:c.1742+256_1742+299del	XP_011528728.1:n.1742+256_1742+299del
XR_244390.1:n.1850+256_1850+299del
XR_430411.1:n.1902+256_1902+299del
XR_937937.1:n.1850+256_1850+299del
XR_937938.1:n.1936+256_1936+299del
XR_937939.1:n.1902+256_1902+299del
NM_001004426.2:c.1580+256_1580+299del	NP_001004426.1:n.1580+256_1580+299del
NM_001199562.2:c.1580+256_1580+299del	NP_001186491.1:n.1580+256_1580+299del
NM_001349864.1:c.1742+256_1742+299del	NP_001336793.1:n.1742+256_1742+299del
NM_001349865.1:c.1580+256_1580+299del	NP_001336794.1:n.1580+256_1580+299del
NM_001349866.1:c.1580+256_1580+299del	NP_001336795.1:n.1580+256_1580+299del
NM_001349867.1:c.1208+256_1208+299del	NP_001336796.1:n.1208+256_1208+299del
NM_001349868.1:c.1064+256_1064+299del	NP_001336797.1:n.1064+256_1064+299del
NM_001349869.1:c.1046+256_1046+299del	NP_001336798.1:n.1046+256_1046+299del
NM_003560.3:c.1742+256_1742+299del	NP_003551.2:n.1742+256_1742+299del
XM_005261764.3:c.1742+256_1742+299del	XP_005261821.1:n.1742+256_1742+299del
XM_005261765.2:c.1742+256_1742+299del	XP_005261822.1:n.1742+256_1742+299del
XM_006724332.4:c.1742+256_1742+299del	XP_006724395.1:n.1742+256_1742+299del
XM_011530426.3:c.1742+256_1742+299del	XP_011528728.1:n.1742+256_1742+299del
XM_017028983.1:c.1046+256_1046+299del	XP_016884472.1:n.1046+256_1046+299del
XM_017028986.2:c.1580+256_1580+299del	XP_016884475.1:n.1580+256_1580+299del
XM_024452280.1:c.1208+256_1208+299del	XP_024308048.1:n.1208+256_1208+299del
XM_024452281.1:c.1208+256_1208+299del	XP_024308049.1:n.1208+256_1208+299del
XM_024452282.1:c.1208+256_1208+299del	XP_024308050.1:n.1208+256_1208+299del
XM_024452283.1:c.1064+256_1064+299del	XP_024308051.1:n.1064+256_1064+299del
XM_024452284.1:c.1046+256_1046+299del	XP_024308052.1:n.1046+256_1046+299del
XM_024452285.1:c.1046+256_1046+299del	XP_024308053.1:n.1046+256_1046+299del
XR_001755325.2:n.1834+256_1834+299del
XR_001755327.2:n.1920+256_1920+299del
XR_001755328.2:n.1886+256_1886+299del
XR_244390.3:n.1834+256_1834+299del
XR_937938.3:n.1920+256_1920+299del
XR_937939.3:n.1886+256_1886+299del
NM_001199562.3:c.1580+256_1580+299del	NP_001186491.1:n.1580+256_1580+299del
NM_001349864.2:c.1742+256_1742+299del	NP_001336793.1:n.1742+256_1742+299del
NM_001349865.2:c.1580+256_1580+299del	NP_001336794.1:n.1580+256_1580+299del
NM_001349866.2:c.1580+256_1580+299del	NP_001336795.1:n.1580+256_1580+299del
NM_001349867.2:c.1208+256_1208+299del	NP_001336796.1:n.1208+256_1208+299del
NM_001349868.2:c.1064+256_1064+299del	NP_001336797.1:n.1064+256_1064+299del
NM_001349869.2:c.1046+256_1046+299del	NP_001336798.1:n.1046+256_1046+299del
NM_003560.4:c.1742+256_1742+299del MANE Select	NP_003551.2:n.1742+256_1742+299del
NM_001004426.3:c.1580+256_1580+299del	NP_001004426.1:n.1580+256_1580+299del