Canonical Allele Identifier: CA411527798

Gene: PLA2G6

Linked Data

• gnomAD v4: 22-38123112-G-T
• MyVariant Identifiers: chr22:g.38519119G>T (hg19) ; chr22:g.38123112G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38123112G>T , CM000684.2:g.38123112G>T	GRCh38
NC_000022.10:g.38519119G>T , CM000684.1:g.38519119G>T	GRCh37
NC_000022.9:g.36849065G>T	NCBI36
NG_007094.2:g.87579C>A
NG_007094.3:g.96667C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1574C>A MANE Select	ENSP00000333142.3:p.Ala525Asp
ENST00000427114.6:c.878C>A	ENSP00000407743.2:p.Ala293Asp
ENST00000436218.6:c.*772C>A	ENSP00000401242.1:n.*772C>A
ENST00000655142.1:c.*432C>A	ENSP00000499715.1:n.*432C>A
ENST00000660610.1:c.1574C>A	ENSP00000499555.1:p.Ala525Asp
ENST00000663895.1:c.1574C>A	ENSP00000499712.1:p.Ala525Asp
ENST00000664587.1:c.1436C>A	ENSP00000499394.1:p.Ala479Asp
ENST00000665987.1:c.*1313C>A	ENSP00000499423.1:n.*1313C>A
ENST00000667521.1:c.1574C>A	ENSP00000499665.1:p.Ala525Asp
ENST00000668208.1:n.1542C>A
ENST00000668499.1:c.*1296C>A	ENSP00000499626.1:n.*1296C>A
ENST00000668949.1:c.1412C>A	ENSP00000499711.1:p.Ala471Asp
ENST00000671093.1:n.1506C>A
ENST00000673413.1:c.*1243C>A	ENSP00000500600.1:n.*1243C>A
ENST00000332509.7:c.1574C>A	ENSP00000333142.3:p.Ala525Asp
ENST00000335539.7:c.1412C>A	ENSP00000335149.3:p.Ala471Asp
ENST00000402064.5:c.1412C>A	ENSP00000386100.1:p.Ala471Asp
ENST00000448094.5:c.*179C>A	ENSP00000407106.1:n.*179C>A
ENST00000454670.1:c.219C>A
ENST00000491986.1:n.585C>A
NM_001004426.1:c.1412C>A	NP_001004426.1:p.Ala471Asp
NM_001199562.1:c.1412C>A	NP_001186491.1:p.Ala471Asp
NM_003560.2:c.1574C>A	NP_003551.2:p.Ala525Asp
XM_005261764.1:c.1574C>A	XP_005261821.1:p.Ala525Asp
XM_005261765.1:c.1574C>A	XP_005261822.1:p.Ala525Asp
XM_005261766.1:c.1574C>A	XP_005261823.1:p.Ala525Asp
XM_006724332.2:c.1574C>A	XP_006724395.1:p.Ala525Asp
XM_011530422.1:c.1469C>A	XP_011528724.1:p.Ala490Asp
XM_011530423.1:c.1040C>A	XP_011528725.1:p.Ala347Asp
XM_011530424.1:c.1040C>A	XP_011528726.1:p.Ala347Asp
XM_011530425.1:c.1040C>A	XP_011528727.1:p.Ala347Asp
XM_011530426.1:c.1574C>A	XP_011528728.1:p.Ala525Asp
XR_244390.1:n.1682C>A
XR_244392.1:n.1735C>A
XR_430411.1:n.1734C>A
XR_430412.1:n.1787C>A
XR_937937.1:n.1682C>A
XR_937938.1:n.1682C>A
XR_937939.1:n.1734C>A
XR_937940.1:n.1734C>A
NM_001004426.2:c.1412C>A	NP_001004426.1:p.Ala471Asp
NM_001199562.2:c.1412C>A	NP_001186491.1:p.Ala471Asp
NM_001349864.1:c.1574C>A	NP_001336793.1:p.Ala525Asp
NM_001349865.1:c.1412C>A	NP_001336794.1:p.Ala471Asp
NM_001349866.1:c.1412C>A	NP_001336795.1:p.Ala471Asp
NM_001349867.1:c.1040C>A	NP_001336796.1:p.Ala347Asp
NM_001349868.1:c.896C>A	NP_001336797.1:p.Ala299Asp
NM_001349869.1:c.878C>A	NP_001336798.1:p.Ala293Asp
NM_003560.3:c.1574C>A	NP_003551.2:p.Ala525Asp
XM_005261764.3:c.1574C>A	XP_005261821.1:p.Ala525Asp
XM_005261765.2:c.1574C>A	XP_005261822.1:p.Ala525Asp
XM_006724332.4:c.1574C>A	XP_006724395.1:p.Ala525Asp
XM_011530426.3:c.1574C>A	XP_011528728.1:p.Ala525Asp
XM_017028983.1:c.878C>A	XP_016884472.1:p.Ala293Asp
XM_017028986.2:c.1412C>A	XP_016884475.1:p.Ala471Asp
XM_024452280.1:c.1040C>A	XP_024308048.1:p.Ala347Asp
XM_024452281.1:c.1040C>A	XP_024308049.1:p.Ala347Asp
XM_024452282.1:c.1040C>A	XP_024308050.1:p.Ala347Asp
XM_024452283.1:c.896C>A	XP_024308051.1:p.Ala299Asp
XM_024452284.1:c.878C>A	XP_024308052.1:p.Ala293Asp
XM_024452285.1:c.878C>A	XP_024308053.1:p.Ala293Asp
XR_001755325.2:n.1666C>A
XR_001755327.2:n.1666C>A
XR_001755328.2:n.1718C>A
XR_244390.3:n.1666C>A
XR_937938.3:n.1666C>A
XR_937939.3:n.1718C>A
XR_937940.3:n.1718C>A
NM_001199562.3:c.1412C>A	NP_001186491.1:p.Ala471Asp
NM_001349864.2:c.1574C>A	NP_001336793.1:p.Ala525Asp
NM_001349865.2:c.1412C>A	NP_001336794.1:p.Ala471Asp
NM_001349866.2:c.1412C>A	NP_001336795.1:p.Ala471Asp
NM_001349867.2:c.1040C>A	NP_001336796.1:p.Ala347Asp
NM_001349868.2:c.896C>A	NP_001336797.1:p.Ala299Asp
NM_001349869.2:c.878C>A	NP_001336798.1:p.Ala293Asp
NM_003560.4:c.1574C>A MANE Select	NP_003551.2:p.Ala525Asp
NM_001004426.3:c.1412C>A	NP_001004426.1:p.Ala471Asp