Canonical Allele Identifier: CA411525404

Gene: PLA2G6

Linked Data

• MyVariant Identifiers: chr22:g.38512094C>T (hg19) ; chr22:g.38116087C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38116087C>T , CM000684.2:g.38116087C>T	GRCh38
NC_000022.10:g.38512094C>T , CM000684.1:g.38512094C>T	GRCh37
NC_000022.9:g.36842040C>T	NCBI36
NG_007094.2:g.94604G>A
NG_007094.3:g.103692G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1867G>A MANE Select	ENSP00000333142.3:p.Ala623Thr
ENST00000427114.6:c.1171G>A	ENSP00000407743.2:p.Ala391Thr
ENST00000436218.6:c.*1065G>A	ENSP00000401242.1:n.*1065G>A
ENST00000655142.1:c.*725G>A	ENSP00000499715.1:n.*725G>A
ENST00000660610.1:c.1867G>A	ENSP00000499555.1:p.Ala623Thr
ENST00000663895.1:c.1867G>A	ENSP00000499712.1:p.Ala623Thr
ENST00000664587.1:c.1729G>A	ENSP00000499394.1:p.Ala577Thr
ENST00000665987.1:c.*1606G>A	ENSP00000499423.1:n.*1606G>A
ENST00000667521.1:c.1867G>A	ENSP00000499665.1:p.Ala623Thr
ENST00000668499.1:c.*1589G>A	ENSP00000499626.1:n.*1589G>A
ENST00000668949.1:c.1705G>A	ENSP00000499711.1:p.Ala569Thr
ENST00000671093.1:n.1799G>A
ENST00000673413.1:c.*1536G>A	ENSP00000500600.1:n.*1536G>A
ENST00000332509.7:c.1867G>A	ENSP00000333142.3:p.Ala623Thr
ENST00000335539.7:c.1705G>A	ENSP00000335149.3:p.Ala569Thr
ENST00000402064.5:c.1705G>A	ENSP00000386100.1:p.Ala569Thr
ENST00000454670.1:c.603G>A
ENST00000496409.1:n.407G>A
NM_001004426.1:c.1705G>A	NP_001004426.1:p.Ala569Thr
NM_001199562.1:c.1705G>A	NP_001186491.1:p.Ala569Thr
NM_003560.2:c.1867G>A	NP_003551.2:p.Ala623Thr
XM_005261764.1:c.1867G>A	XP_005261821.1:p.Ala623Thr
XM_005261765.1:c.1867G>A	XP_005261822.1:p.Ala623Thr
XM_005261766.1:c.1867G>A	XP_005261823.1:p.Ala623Thr
XM_006724332.2:c.1867G>A	XP_006724395.1:p.Ala623Thr
XM_011530422.1:c.1762G>A	XP_011528724.1:p.Ala588Thr
XM_011530423.1:c.1333G>A	XP_011528725.1:p.Ala445Thr
XM_011530424.1:c.1333G>A	XP_011528726.1:p.Ala445Thr
XM_011530425.1:c.1333G>A	XP_011528727.1:p.Ala445Thr
XR_244390.1:n.1975G>A
XR_430411.1:n.2027G>A
XR_937937.1:n.2066G>A
XR_937938.1:n.2061G>A
XR_937939.1:n.2118G>A
NM_001004426.2:c.1705G>A	NP_001004426.1:p.Ala569Thr
NM_001199562.2:c.1705G>A	NP_001186491.1:p.Ala569Thr
NM_001349864.1:c.1867G>A	NP_001336793.1:p.Ala623Thr
NM_001349865.1:c.1705G>A	NP_001336794.1:p.Ala569Thr
NM_001349866.1:c.1705G>A	NP_001336795.1:p.Ala569Thr
NM_001349867.1:c.1333G>A	NP_001336796.1:p.Ala445Thr
NM_001349868.1:c.1189G>A	NP_001336797.1:p.Ala397Thr
NM_001349869.1:c.1171G>A	NP_001336798.1:p.Ala391Thr
NM_003560.3:c.1867G>A	NP_003551.2:p.Ala623Thr
XM_005261764.3:c.1867G>A	XP_005261821.1:p.Ala623Thr
XM_005261765.2:c.1867G>A	XP_005261822.1:p.Ala623Thr
XM_006724332.4:c.1867G>A	XP_006724395.1:p.Ala623Thr
XM_017028983.1:c.1171G>A	XP_016884472.1:p.Ala391Thr
XM_024452280.1:c.1333G>A	XP_024308048.1:p.Ala445Thr
XM_024452281.1:c.1333G>A	XP_024308049.1:p.Ala445Thr
XM_024452282.1:c.1333G>A	XP_024308050.1:p.Ala445Thr
XM_024452283.1:c.1189G>A	XP_024308051.1:p.Ala397Thr
XM_024452284.1:c.1171G>A	XP_024308052.1:p.Ala391Thr
XM_024452285.1:c.1171G>A	XP_024308053.1:p.Ala391Thr
XR_001755325.2:n.2050G>A
XR_001755327.2:n.2045G>A
XR_001755328.2:n.2011G>A
XR_244390.3:n.1959G>A
XR_937938.3:n.2045G>A
XR_937939.3:n.2102G>A
NM_001199562.3:c.1705G>A	NP_001186491.1:p.Ala569Thr
NM_001349864.2:c.1867G>A	NP_001336793.1:p.Ala623Thr
NM_001349865.2:c.1705G>A	NP_001336794.1:p.Ala569Thr
NM_001349866.2:c.1705G>A	NP_001336795.1:p.Ala569Thr
NM_001349867.2:c.1333G>A	NP_001336796.1:p.Ala445Thr
NM_001349868.2:c.1189G>A	NP_001336797.1:p.Ala397Thr
NM_001349869.2:c.1171G>A	NP_001336798.1:p.Ala391Thr
NM_003560.4:c.1867G>A MANE Select	NP_003551.2:p.Ala623Thr
NM_001004426.3:c.1705G>A	NP_001004426.1:p.Ala569Thr