Canonical Allele Identifier: CA411525828

Gene: PLA2G6

Linked Data

• ClinVar Variation Id: 2187652
• ClinVar RCV Id: RCV002623585
• MyVariant Identifiers: chr22:g.38512214T>A (hg19) ; chr22:g.38116207T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38116207T>A , CM000684.2:g.38116207T>A	GRCh38
NC_000022.10:g.38512214T>A , CM000684.1:g.38512214T>A	GRCh37
NC_000022.9:g.36842160T>A	NCBI36
NG_007094.2:g.94484A>T
NG_007094.3:g.103572A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1747A>T MANE Select	ENSP00000333142.3:p.Met583Leu
ENST00000427114.6:c.1051A>T	ENSP00000407743.2:p.Met351Leu
ENST00000436218.6:c.*945A>T	ENSP00000401242.1:n.*945A>T
ENST00000655142.1:c.*605A>T	ENSP00000499715.1:n.*605A>T
ENST00000660610.1:c.1747A>T	ENSP00000499555.1:p.Met583Leu
ENST00000663895.1:c.1747A>T	ENSP00000499712.1:p.Met583Leu
ENST00000664587.1:c.1609A>T	ENSP00000499394.1:p.Met537Leu
ENST00000665987.1:c.*1486A>T	ENSP00000499423.1:n.*1486A>T
ENST00000667521.1:c.1747A>T	ENSP00000499665.1:p.Met583Leu
ENST00000668499.1:c.*1469A>T	ENSP00000499626.1:n.*1469A>T
ENST00000668949.1:c.1585A>T	ENSP00000499711.1:p.Met529Leu
ENST00000671093.1:n.1679A>T
ENST00000673413.1:c.*1416A>T	ENSP00000500600.1:n.*1416A>T
ENST00000332509.7:c.1747A>T	ENSP00000333142.3:p.Met583Leu
ENST00000335539.7:c.1585A>T	ENSP00000335149.3:p.Met529Leu
ENST00000402064.5:c.1585A>T	ENSP00000386100.1:p.Met529Leu
ENST00000448094.5:c.*352A>T	ENSP00000407106.1:n.*352A>T
ENST00000454670.1:c.483A>T
ENST00000496409.1:n.287A>T
NM_001004426.1:c.1585A>T	NP_001004426.1:p.Met529Leu
NM_001199562.1:c.1585A>T	NP_001186491.1:p.Met529Leu
NM_003560.2:c.1747A>T	NP_003551.2:p.Met583Leu
XM_005261764.1:c.1747A>T	XP_005261821.1:p.Met583Leu
XM_005261765.1:c.1747A>T	XP_005261822.1:p.Met583Leu
XM_005261766.1:c.1747A>T	XP_005261823.1:p.Met583Leu
XM_006724332.2:c.1747A>T	XP_006724395.1:p.Met583Leu
XM_011530422.1:c.1642A>T	XP_011528724.1:p.Met548Leu
XM_011530423.1:c.1213A>T	XP_011528725.1:p.Met405Leu
XM_011530424.1:c.1213A>T	XP_011528726.1:p.Met405Leu
XM_011530425.1:c.1213A>T	XP_011528727.1:p.Met405Leu
XR_244390.1:n.1855A>T
XR_430411.1:n.1907A>T
XR_937937.1:n.1946A>T
XR_937938.1:n.1941A>T
XR_937939.1:n.1998A>T
NM_001004426.2:c.1585A>T	NP_001004426.1:p.Met529Leu
NM_001199562.2:c.1585A>T	NP_001186491.1:p.Met529Leu
NM_001349864.1:c.1747A>T	NP_001336793.1:p.Met583Leu
NM_001349865.1:c.1585A>T	NP_001336794.1:p.Met529Leu
NM_001349866.1:c.1585A>T	NP_001336795.1:p.Met529Leu
NM_001349867.1:c.1213A>T	NP_001336796.1:p.Met405Leu
NM_001349868.1:c.1069A>T	NP_001336797.1:p.Met357Leu
NM_001349869.1:c.1051A>T	NP_001336798.1:p.Met351Leu
NM_003560.3:c.1747A>T	NP_003551.2:p.Met583Leu
XM_005261764.3:c.1747A>T	XP_005261821.1:p.Met583Leu
XM_005261765.2:c.1747A>T	XP_005261822.1:p.Met583Leu
XM_006724332.4:c.1747A>T	XP_006724395.1:p.Met583Leu
XM_017028983.1:c.1051A>T	XP_016884472.1:p.Met351Leu
XM_024452280.1:c.1213A>T	XP_024308048.1:p.Met405Leu
XM_024452281.1:c.1213A>T	XP_024308049.1:p.Met405Leu
XM_024452282.1:c.1213A>T	XP_024308050.1:p.Met405Leu
XM_024452283.1:c.1069A>T	XP_024308051.1:p.Met357Leu
XM_024452284.1:c.1051A>T	XP_024308052.1:p.Met351Leu
XM_024452285.1:c.1051A>T	XP_024308053.1:p.Met351Leu
XR_001755325.2:n.1930A>T
XR_001755327.2:n.1925A>T
XR_001755328.2:n.1891A>T
XR_244390.3:n.1839A>T
XR_937938.3:n.1925A>T
XR_937939.3:n.1982A>T
NM_001199562.3:c.1585A>T	NP_001186491.1:p.Met529Leu
NM_001349864.2:c.1747A>T	NP_001336793.1:p.Met583Leu
NM_001349865.2:c.1585A>T	NP_001336794.1:p.Met529Leu
NM_001349866.2:c.1585A>T	NP_001336795.1:p.Met529Leu
NM_001349867.2:c.1213A>T	NP_001336796.1:p.Met405Leu
NM_001349868.2:c.1069A>T	NP_001336797.1:p.Met357Leu
NM_001349869.2:c.1051A>T	NP_001336798.1:p.Met351Leu
NM_003560.4:c.1747A>T MANE Select	NP_003551.2:p.Met583Leu
NM_001004426.3:c.1585A>T	NP_001004426.1:p.Met529Leu