Canonical Allele Identifier: CA2404668386

Gene: PLA2G6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38113588C= , CM000684.2:g.38113588C=	GRCh38
NC_000022.10:g.38509595C= , CM000684.1:g.38509595C=	GRCh37
NC_000022.9:g.36839541C=	NCBI36
NG_007094.2:g.97103G=
NG_033059.2:g.2082G=
NG_007094.3:g.106191G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.2101G= MANE Select	ENSP00000333142.3:p.Val701=
ENST00000436218.6:c.*1299G=	ENSP00000401242.1:n.*1299G=
ENST00000655142.1:c.*959G=	ENSP00000499715.1:n.*959G=
ENST00000660610.1:c.2101G=	ENSP00000499555.1:p.Val701=
ENST00000663895.1:c.2101G=	ENSP00000499712.1:p.Val701=
ENST00000664587.1:c.1963G=	ENSP00000499394.1:p.Val655=
ENST00000665987.1:c.*1840G=	ENSP00000499423.1:n.*1840G=
ENST00000667521.1:c.2101G=	ENSP00000499665.1:p.Val701=
ENST00000668499.1:c.*1960G=	ENSP00000499626.1:n.*1960G=
ENST00000668949.1:c.2143G=	ENSP00000499711.1:p.Val715=
ENST00000671093.1:n.2033G=
ENST00000673413.1:c.*1770G=	ENSP00000500600.1:n.*1770G=
ENST00000332509.7:c.2101G=	ENSP00000333142.3:p.Val701=
ENST00000335539.7:c.1939G=	ENSP00000335149.3:p.Val647=
ENST00000402064.5:c.1939G=	ENSP00000386100.1:p.Val647=
ENST00000496409.1:n.809G=
NM_001004426.1:c.1939G=	NP_001004426.1:p.Val647=
NM_001199562.1:c.1939G=	NP_001186491.1:p.Val647=
NM_003560.2:c.2101G=	NP_003551.2:p.Val701=
XM_005261764.1:c.2101G=	XP_005261821.1:p.Val701=
XM_005261765.1:c.2101G=	XP_005261822.1:p.Val701=
XM_005261766.1:c.2101G=	XP_005261823.1:p.Val701=
XM_006724332.2:c.2101G=	XP_006724395.1:p.Val701=
XM_011530422.1:c.1996G=	XP_011528724.1:p.Val666=
XM_011530423.1:c.1567G=	XP_011528725.1:p.Val523=
XM_011530424.1:c.1567G=	XP_011528726.1:p.Val523=
XM_011530425.1:c.1567G=	XP_011528727.1:p.Val523=
XR_244390.1:n.2377G=
XR_430411.1:n.2261G=
XR_937938.1:n.2463G=
NM_001004426.2:c.1939G=	NP_001004426.1:p.Val647=
NM_001199562.2:c.1939G=	NP_001186491.1:p.Val647=
NM_001349864.1:c.2101G=	NP_001336793.1:p.Val701=
NM_001349865.1:c.1939G=	NP_001336794.1:p.Val647=
NM_001349866.1:c.1939G=	NP_001336795.1:p.Val647=
NM_001349867.1:c.1567G=	NP_001336796.1:p.Val523=
NM_001349868.1:c.1423G=	NP_001336797.1:p.Val475=
NM_001349869.1:c.1405G=	NP_001336798.1:p.Val469=
NM_003560.3:c.2101G=	NP_003551.2:p.Val701=
XM_005261764.3:c.2101G=	XP_005261821.1:p.Val701=
XM_005261765.2:c.2101G=	XP_005261822.1:p.Val701=
XM_006724332.4:c.2101G=	XP_006724395.1:p.Val701=
XM_017028983.1:c.1405G=	XP_016884472.1:p.Val469=
XM_024452280.1:c.1567G=	XP_024308048.1:p.Val523=
XM_024452281.1:c.1567G=	XP_024308049.1:p.Val523=
XM_024452282.1:c.1567G=	XP_024308050.1:p.Val523=
XM_024452283.1:c.1423G=	XP_024308051.1:p.Val475=
XM_024452284.1:c.1405G=	XP_024308052.1:p.Val469=
XM_024452285.1:c.1405G=	XP_024308053.1:p.Val469=
XR_001755325.2:n.2284G=
XR_001755327.2:n.2279G=
XR_001755328.2:n.2245G=
XR_244390.3:n.2361G=
XR_937938.3:n.2447G=
NM_001199562.3:c.1939G=	NP_001186491.1:p.Val647=
NM_001349864.2:c.2101G=	NP_001336793.1:p.Val701=
NM_001349865.2:c.1939G=	NP_001336794.1:p.Val647=
NM_001349866.2:c.1939G=	NP_001336795.1:p.Val647=
NM_001349867.2:c.1567G=	NP_001336796.1:p.Val523=
NM_001349868.2:c.1423G=	NP_001336797.1:p.Val475=
NM_001349869.2:c.1405G=	NP_001336798.1:p.Val469=
NM_003560.4:c.2101G= MANE Select	NP_003551.2:p.Val701=
NM_001004426.3:c.1939G=	NP_001004426.1:p.Val647=