Canonical Allele Identifier: CA411525592

Gene: PLA2G6

Linked Data

• gnomAD v4: 22-38116134-G-A
• MyVariant Identifiers: chr22:g.38512141G>A (hg19) ; chr22:g.38116134G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38116134G>A , CM000684.2:g.38116134G>A	GRCh38
NC_000022.10:g.38512141G>A , CM000684.1:g.38512141G>A	GRCh37
NC_000022.9:g.36842087G>A	NCBI36
NG_007094.2:g.94557C>T
NG_007094.3:g.103645C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1820C>T MANE Select	ENSP00000333142.3:p.Thr607Ile
ENST00000427114.6:c.1124C>T	ENSP00000407743.2:p.Thr375Ile
ENST00000436218.6:c.*1018C>T	ENSP00000401242.1:n.*1018C>T
ENST00000655142.1:c.*678C>T	ENSP00000499715.1:n.*678C>T
ENST00000660610.1:c.1820C>T	ENSP00000499555.1:p.Thr607Ile
ENST00000663895.1:c.1820C>T	ENSP00000499712.1:p.Thr607Ile
ENST00000664587.1:c.1682C>T	ENSP00000499394.1:p.Thr561Ile
ENST00000665987.1:c.*1559C>T	ENSP00000499423.1:n.*1559C>T
ENST00000667521.1:c.1820C>T	ENSP00000499665.1:p.Thr607Ile
ENST00000668499.1:c.*1542C>T	ENSP00000499626.1:n.*1542C>T
ENST00000668949.1:c.1658C>T	ENSP00000499711.1:p.Thr553Ile
ENST00000671093.1:n.1752C>T
ENST00000673413.1:c.*1489C>T	ENSP00000500600.1:n.*1489C>T
ENST00000332509.7:c.1820C>T	ENSP00000333142.3:p.Thr607Ile
ENST00000335539.7:c.1658C>T	ENSP00000335149.3:p.Thr553Ile
ENST00000402064.5:c.1658C>T	ENSP00000386100.1:p.Thr553Ile
ENST00000448094.5:c.*425C>T	ENSP00000407106.1:n.*425C>T
ENST00000454670.1:c.556C>T
ENST00000496409.1:n.360C>T
NM_001004426.1:c.1658C>T	NP_001004426.1:p.Thr553Ile
NM_001199562.1:c.1658C>T	NP_001186491.1:p.Thr553Ile
NM_003560.2:c.1820C>T	NP_003551.2:p.Thr607Ile
XM_005261764.1:c.1820C>T	XP_005261821.1:p.Thr607Ile
XM_005261765.1:c.1820C>T	XP_005261822.1:p.Thr607Ile
XM_005261766.1:c.1820C>T	XP_005261823.1:p.Thr607Ile
XM_006724332.2:c.1820C>T	XP_006724395.1:p.Thr607Ile
XM_011530422.1:c.1715C>T	XP_011528724.1:p.Thr572Ile
XM_011530423.1:c.1286C>T	XP_011528725.1:p.Thr429Ile
XM_011530424.1:c.1286C>T	XP_011528726.1:p.Thr429Ile
XM_011530425.1:c.1286C>T	XP_011528727.1:p.Thr429Ile
XR_244390.1:n.1928C>T
XR_430411.1:n.1980C>T
XR_937937.1:n.2019C>T
XR_937938.1:n.2014C>T
XR_937939.1:n.2071C>T
NM_001004426.2:c.1658C>T	NP_001004426.1:p.Thr553Ile
NM_001199562.2:c.1658C>T	NP_001186491.1:p.Thr553Ile
NM_001349864.1:c.1820C>T	NP_001336793.1:p.Thr607Ile
NM_001349865.1:c.1658C>T	NP_001336794.1:p.Thr553Ile
NM_001349866.1:c.1658C>T	NP_001336795.1:p.Thr553Ile
NM_001349867.1:c.1286C>T	NP_001336796.1:p.Thr429Ile
NM_001349868.1:c.1142C>T	NP_001336797.1:p.Thr381Ile
NM_001349869.1:c.1124C>T	NP_001336798.1:p.Thr375Ile
NM_003560.3:c.1820C>T	NP_003551.2:p.Thr607Ile
XM_005261764.3:c.1820C>T	XP_005261821.1:p.Thr607Ile
XM_005261765.2:c.1820C>T	XP_005261822.1:p.Thr607Ile
XM_006724332.4:c.1820C>T	XP_006724395.1:p.Thr607Ile
XM_017028983.1:c.1124C>T	XP_016884472.1:p.Thr375Ile
XM_024452280.1:c.1286C>T	XP_024308048.1:p.Thr429Ile
XM_024452281.1:c.1286C>T	XP_024308049.1:p.Thr429Ile
XM_024452282.1:c.1286C>T	XP_024308050.1:p.Thr429Ile
XM_024452283.1:c.1142C>T	XP_024308051.1:p.Thr381Ile
XM_024452284.1:c.1124C>T	XP_024308052.1:p.Thr375Ile
XM_024452285.1:c.1124C>T	XP_024308053.1:p.Thr375Ile
XR_001755325.2:n.2003C>T
XR_001755327.2:n.1998C>T
XR_001755328.2:n.1964C>T
XR_244390.3:n.1912C>T
XR_937938.3:n.1998C>T
XR_937939.3:n.2055C>T
NM_001199562.3:c.1658C>T	NP_001186491.1:p.Thr553Ile
NM_001349864.2:c.1820C>T	NP_001336793.1:p.Thr607Ile
NM_001349865.2:c.1658C>T	NP_001336794.1:p.Thr553Ile
NM_001349866.2:c.1658C>T	NP_001336795.1:p.Thr553Ile
NM_001349867.2:c.1286C>T	NP_001336796.1:p.Thr429Ile
NM_001349868.2:c.1142C>T	NP_001336797.1:p.Thr381Ile
NM_001349869.2:c.1124C>T	NP_001336798.1:p.Thr375Ile
NM_003560.4:c.1820C>T MANE Select	NP_003551.2:p.Thr607Ile
NM_001004426.3:c.1658C>T	NP_001004426.1:p.Thr553Ile