Canonical Allele Identifier: CA411525638

Gene: PLA2G6

Linked Data

• MyVariant Identifiers: chr22:g.38512152A>T (hg19) ; chr22:g.38116145A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38116145A>T , CM000684.2:g.38116145A>T	GRCh38
NC_000022.10:g.38512152A>T , CM000684.1:g.38512152A>T	GRCh37
NC_000022.9:g.36842098A>T	NCBI36
NG_007094.2:g.94546T>A
NG_007094.3:g.103634T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1809T>A MANE Select	ENSP00000333142.3:p.Asp603Glu
ENST00000427114.6:c.1113T>A	ENSP00000407743.2:p.Asp371Glu
ENST00000436218.6:c.*1007T>A	ENSP00000401242.1:n.*1007T>A
ENST00000655142.1:c.*667T>A	ENSP00000499715.1:n.*667T>A
ENST00000660610.1:c.1809T>A	ENSP00000499555.1:p.Asp603Glu
ENST00000663895.1:c.1809T>A	ENSP00000499712.1:p.Asp603Glu
ENST00000664587.1:c.1671T>A	ENSP00000499394.1:p.Asp557Glu
ENST00000665987.1:c.*1548T>A	ENSP00000499423.1:n.*1548T>A
ENST00000667521.1:c.1809T>A	ENSP00000499665.1:p.Asp603Glu
ENST00000668499.1:c.*1531T>A	ENSP00000499626.1:n.*1531T>A
ENST00000668949.1:c.1647T>A	ENSP00000499711.1:p.Asp549Glu
ENST00000671093.1:n.1741T>A
ENST00000673413.1:c.*1478T>A	ENSP00000500600.1:n.*1478T>A
ENST00000332509.7:c.1809T>A	ENSP00000333142.3:p.Asp603Glu
ENST00000335539.7:c.1647T>A	ENSP00000335149.3:p.Asp549Glu
ENST00000402064.5:c.1647T>A	ENSP00000386100.1:p.Asp549Glu
ENST00000448094.5:c.*414T>A	ENSP00000407106.1:n.*414T>A
ENST00000454670.1:c.545T>A
ENST00000496409.1:n.349T>A
NM_001004426.1:c.1647T>A	NP_001004426.1:p.Asp549Glu
NM_001199562.1:c.1647T>A	NP_001186491.1:p.Asp549Glu
NM_003560.2:c.1809T>A	NP_003551.2:p.Asp603Glu
XM_005261764.1:c.1809T>A	XP_005261821.1:p.Asp603Glu
XM_005261765.1:c.1809T>A	XP_005261822.1:p.Asp603Glu
XM_005261766.1:c.1809T>A	XP_005261823.1:p.Asp603Glu
XM_006724332.2:c.1809T>A	XP_006724395.1:p.Asp603Glu
XM_011530422.1:c.1704T>A	XP_011528724.1:p.Asp568Glu
XM_011530423.1:c.1275T>A	XP_011528725.1:p.Asp425Glu
XM_011530424.1:c.1275T>A	XP_011528726.1:p.Asp425Glu
XM_011530425.1:c.1275T>A	XP_011528727.1:p.Asp425Glu
XR_244390.1:n.1917T>A
XR_430411.1:n.1969T>A
XR_937937.1:n.2008T>A
XR_937938.1:n.2003T>A
XR_937939.1:n.2060T>A
NM_001004426.2:c.1647T>A	NP_001004426.1:p.Asp549Glu
NM_001199562.2:c.1647T>A	NP_001186491.1:p.Asp549Glu
NM_001349864.1:c.1809T>A	NP_001336793.1:p.Asp603Glu
NM_001349865.1:c.1647T>A	NP_001336794.1:p.Asp549Glu
NM_001349866.1:c.1647T>A	NP_001336795.1:p.Asp549Glu
NM_001349867.1:c.1275T>A	NP_001336796.1:p.Asp425Glu
NM_001349868.1:c.1131T>A	NP_001336797.1:p.Asp377Glu
NM_001349869.1:c.1113T>A	NP_001336798.1:p.Asp371Glu
NM_003560.3:c.1809T>A	NP_003551.2:p.Asp603Glu
XM_005261764.3:c.1809T>A	XP_005261821.1:p.Asp603Glu
XM_005261765.2:c.1809T>A	XP_005261822.1:p.Asp603Glu
XM_006724332.4:c.1809T>A	XP_006724395.1:p.Asp603Glu
XM_017028983.1:c.1113T>A	XP_016884472.1:p.Asp371Glu
XM_024452280.1:c.1275T>A	XP_024308048.1:p.Asp425Glu
XM_024452281.1:c.1275T>A	XP_024308049.1:p.Asp425Glu
XM_024452282.1:c.1275T>A	XP_024308050.1:p.Asp425Glu
XM_024452283.1:c.1131T>A	XP_024308051.1:p.Asp377Glu
XM_024452284.1:c.1113T>A	XP_024308052.1:p.Asp371Glu
XM_024452285.1:c.1113T>A	XP_024308053.1:p.Asp371Glu
XR_001755325.2:n.1992T>A
XR_001755327.2:n.1987T>A
XR_001755328.2:n.1953T>A
XR_244390.3:n.1901T>A
XR_937938.3:n.1987T>A
XR_937939.3:n.2044T>A
NM_001199562.3:c.1647T>A	NP_001186491.1:p.Asp549Glu
NM_001349864.2:c.1809T>A	NP_001336793.1:p.Asp603Glu
NM_001349865.2:c.1647T>A	NP_001336794.1:p.Asp549Glu
NM_001349866.2:c.1647T>A	NP_001336795.1:p.Asp549Glu
NM_001349867.2:c.1275T>A	NP_001336796.1:p.Asp425Glu
NM_001349868.2:c.1131T>A	NP_001336797.1:p.Asp377Glu
NM_001349869.2:c.1113T>A	NP_001336798.1:p.Asp371Glu
NM_003560.4:c.1809T>A MANE Select	NP_003551.2:p.Asp603Glu
NM_001004426.3:c.1647T>A	NP_001004426.1:p.Asp549Glu