Canonical Allele Identifier: CA411523192

Gene: PLA2G6

Linked Data

• MyVariant Identifiers: chr22:g.38508277T>A (hg19) ; chr22:g.38112270T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38112270T>A , CM000684.2:g.38112270T>A	GRCh38
NC_000022.10:g.38508277T>A , CM000684.1:g.38508277T>A	GRCh37
NC_000022.9:g.36838223T>A	NCBI36
NG_007094.2:g.98421A>T
NG_033059.2:g.3400A>T
NG_007094.3:g.107509A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.2312A>T MANE Select	ENSP00000333142.3:p.Asp771Val
ENST00000436218.6:c.*1510A>T	ENSP00000401242.1:n.*1510A>T
ENST00000655142.1:c.*1170A>T	ENSP00000499715.1:n.*1170A>T
ENST00000660610.1:c.2312A>T	ENSP00000499555.1:p.Asp771Val
ENST00000663895.1:c.2312A>T	ENSP00000499712.1:p.Asp771Val
ENST00000664587.1:c.2174A>T	ENSP00000499394.1:p.Asp725Val
ENST00000665987.1:c.*2051A>T	ENSP00000499423.1:n.*2051A>T
ENST00000667521.1:c.2312A>T	ENSP00000499665.1:p.Asp771Val
ENST00000668499.1:c.*2171A>T	ENSP00000499626.1:n.*2171A>T
ENST00000668949.1:c.2354A>T	ENSP00000499711.1:p.Asp785Val
ENST00000671093.1:n.2244A>T
ENST00000673413.1:c.*1981A>T	ENSP00000500600.1:n.*1981A>T
ENST00000332509.7:c.2312A>T	ENSP00000333142.3:p.Asp771Val
ENST00000335539.7:c.2150A>T	ENSP00000335149.3:p.Asp717Val
ENST00000402064.5:c.2150A>T	ENSP00000386100.1:p.Asp717Val
ENST00000463287.1:n.388A>T
NM_001004426.1:c.2150A>T	NP_001004426.1:p.Asp717Val
NM_001199562.1:c.2150A>T	NP_001186491.1:p.Asp717Val
NM_003560.2:c.2312A>T	NP_003551.2:p.Asp771Val
XM_005261764.1:c.2312A>T	XP_005261821.1:p.Asp771Val
XM_005261765.1:c.2312A>T	XP_005261822.1:p.Asp771Val
XM_005261766.1:c.2312A>T	XP_005261823.1:p.Asp771Val
XM_006724332.2:c.2312A>T	XP_006724395.1:p.Asp771Val
XM_011530422.1:c.2207A>T	XP_011528724.1:p.Asp736Val
XM_011530423.1:c.1778A>T	XP_011528725.1:p.Asp593Val
XM_011530424.1:c.1778A>T	XP_011528726.1:p.Asp593Val
XM_011530425.1:c.1778A>T	XP_011528727.1:p.Asp593Val
NM_001004426.2:c.2150A>T	NP_001004426.1:p.Asp717Val
NM_001199562.2:c.2150A>T	NP_001186491.1:p.Asp717Val
NM_001349864.1:c.2312A>T	NP_001336793.1:p.Asp771Val
NM_001349865.1:c.2150A>T	NP_001336794.1:p.Asp717Val
NM_001349866.1:c.2150A>T	NP_001336795.1:p.Asp717Val
NM_001349867.1:c.1778A>T	NP_001336796.1:p.Asp593Val
NM_001349868.1:c.1634A>T	NP_001336797.1:p.Asp545Val
NM_001349869.1:c.1616A>T	NP_001336798.1:p.Asp539Val
NM_003560.3:c.2312A>T	NP_003551.2:p.Asp771Val
XM_005261764.3:c.2312A>T	XP_005261821.1:p.Asp771Val
XM_005261765.2:c.2312A>T	XP_005261822.1:p.Asp771Val
XM_006724332.4:c.2312A>T	XP_006724395.1:p.Asp771Val
XM_017028983.1:c.1616A>T	XP_016884472.1:p.Asp539Val
XM_024452280.1:c.1778A>T	XP_024308048.1:p.Asp593Val
XM_024452281.1:c.1778A>T	XP_024308049.1:p.Asp593Val
XM_024452282.1:c.1778A>T	XP_024308050.1:p.Asp593Val
XM_024452283.1:c.1634A>T	XP_024308051.1:p.Asp545Val
XM_024452284.1:c.1616A>T	XP_024308052.1:p.Asp539Val
XM_024452285.1:c.1616A>T	XP_024308053.1:p.Asp539Val
XR_001755325.2:n.2495A>T
XR_001755327.2:n.2490A>T
XR_001755328.2:n.2456A>T
NM_001199562.3:c.2150A>T	NP_001186491.1:p.Asp717Val
NM_001349864.2:c.2312A>T	NP_001336793.1:p.Asp771Val
NM_001349865.2:c.2150A>T	NP_001336794.1:p.Asp717Val
NM_001349866.2:c.2150A>T	NP_001336795.1:p.Asp717Val
NM_001349867.2:c.1778A>T	NP_001336796.1:p.Asp593Val
NM_001349868.2:c.1634A>T	NP_001336797.1:p.Asp545Val
NM_001349869.2:c.1616A>T	NP_001336798.1:p.Asp539Val
NM_003560.4:c.2312A>T MANE Select	NP_003551.2:p.Asp771Val
NM_001004426.3:c.2150A>T	NP_001004426.1:p.Asp717Val