Canonical Allele Identifier: CA324183399

Gene: PLA2G6

Linked Data

• dbSNP Id: rs376610322
• gnomAD v2: 22-38511579-A-G
• gnomAD v4: 22-38115572-A-G
• MyVariant Identifiers: chr22:g.38511579A>G (hg19) ; chr22:g.38115572A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38115572A>G , CM000684.2:g.38115572A>G	GRCh38
NC_000022.10:g.38511579A>G , CM000684.1:g.38511579A>G	GRCh37
NC_000022.9:g.36841525A>G	NCBI36
NG_007094.2:g.95119T>C
NG_033059.2:g.98T>C
NG_007094.3:g.104207T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1989T>C MANE Select	ENSP00000333142.3:p.Asp663=
ENST00000427114.6:c.1293T>C	ENSP00000407743.2:p.Asp431=
ENST00000436218.6:c.*1187T>C	ENSP00000401242.1:n.*1187T>C
ENST00000655142.1:c.*847T>C	ENSP00000499715.1:n.*847T>C
ENST00000660610.1:c.1989T>C	ENSP00000499555.1:p.Asp663=
ENST00000663895.1:c.1989T>C	ENSP00000499712.1:p.Asp663=
ENST00000664587.1:c.1851T>C	ENSP00000499394.1:p.Asp617=
ENST00000665987.1:c.*1728T>C	ENSP00000499423.1:n.*1728T>C
ENST00000667521.1:c.1989T>C	ENSP00000499665.1:p.Asp663=
ENST00000668499.1:c.*1711T>C	ENSP00000499626.1:n.*1711T>C
ENST00000668949.1:c.1827T>C	ENSP00000499711.1:p.Asp609=
ENST00000671093.1:n.1921T>C
ENST00000673413.1:c.*1658T>C	ENSP00000500600.1:n.*1658T>C
ENST00000332509.7:c.1989T>C	ENSP00000333142.3:p.Asp663=
ENST00000335539.7:c.1827T>C	ENSP00000335149.3:p.Asp609=
ENST00000402064.5:c.1827T>C	ENSP00000386100.1:p.Asp609=
ENST00000454670.1:c.725T>C
ENST00000496409.1:n.697T>C
NM_001004426.1:c.1827T>C	NP_001004426.1:p.Asp609=
NM_001199562.1:c.1827T>C	NP_001186491.1:p.Asp609=
NM_003560.2:c.1989T>C	NP_003551.2:p.Asp663=
XM_005261764.1:c.1989T>C	XP_005261821.1:p.Asp663=
XM_005261765.1:c.1989T>C	XP_005261822.1:p.Asp663=
XM_005261766.1:c.1989T>C	XP_005261823.1:p.Asp663=
XM_006724332.2:c.1989T>C	XP_006724395.1:p.Asp663=
XM_011530422.1:c.1884T>C	XP_011528724.1:p.Asp628=
XM_011530423.1:c.1455T>C	XP_011528725.1:p.Asp485=
XM_011530424.1:c.1455T>C	XP_011528726.1:p.Asp485=
XM_011530425.1:c.1455T>C	XP_011528727.1:p.Asp485=
XR_244390.1:n.2265T>C
XR_430411.1:n.2149T>C
XR_937937.1:n.2188T>C
XR_937938.1:n.2351T>C
XR_937939.1:n.2240T>C
NM_001004426.2:c.1827T>C	NP_001004426.1:p.Asp609=
NM_001199562.2:c.1827T>C	NP_001186491.1:p.Asp609=
NM_001349864.1:c.1989T>C	NP_001336793.1:p.Asp663=
NM_001349865.1:c.1827T>C	NP_001336794.1:p.Asp609=
NM_001349866.1:c.1827T>C	NP_001336795.1:p.Asp609=
NM_001349867.1:c.1455T>C	NP_001336796.1:p.Asp485=
NM_001349868.1:c.1311T>C	NP_001336797.1:p.Asp437=
NM_001349869.1:c.1293T>C	NP_001336798.1:p.Asp431=
NM_003560.3:c.1989T>C	NP_003551.2:p.Asp663=
XM_005261764.3:c.1989T>C	XP_005261821.1:p.Asp663=
XM_005261765.2:c.1989T>C	XP_005261822.1:p.Asp663=
XM_006724332.4:c.1989T>C	XP_006724395.1:p.Asp663=
XM_017028983.1:c.1293T>C	XP_016884472.1:p.Asp431=
XM_024452280.1:c.1455T>C	XP_024308048.1:p.Asp485=
XM_024452281.1:c.1455T>C	XP_024308049.1:p.Asp485=
XM_024452282.1:c.1455T>C	XP_024308050.1:p.Asp485=
XM_024452283.1:c.1311T>C	XP_024308051.1:p.Asp437=
XM_024452284.1:c.1293T>C	XP_024308052.1:p.Asp431=
XM_024452285.1:c.1293T>C	XP_024308053.1:p.Asp431=
XR_001755325.2:n.2172T>C
XR_001755327.2:n.2167T>C
XR_001755328.2:n.2133T>C
XR_244390.3:n.2249T>C
XR_937938.3:n.2335T>C
XR_937939.3:n.2224T>C
NM_001199562.3:c.1827T>C	NP_001186491.1:p.Asp609=
NM_001349864.2:c.1989T>C	NP_001336793.1:p.Asp663=
NM_001349865.2:c.1827T>C	NP_001336794.1:p.Asp609=
NM_001349866.2:c.1827T>C	NP_001336795.1:p.Asp609=
NM_001349867.2:c.1455T>C	NP_001336796.1:p.Asp485=
NM_001349868.2:c.1311T>C	NP_001336797.1:p.Asp437=
NM_001349869.2:c.1293T>C	NP_001336798.1:p.Asp431=
NM_003560.4:c.1989T>C MANE Select	NP_003551.2:p.Asp663=
NM_001004426.3:c.1827T>C	NP_001004426.1:p.Asp609=