Canonical Allele Identifier: CA514542433

Gene: PLA2G6

Linked Data

• MyVariant Identifiers: chr22:g.38509599T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38113592T>G , CM000684.2:g.38113592T>G	GRCh38
NC_000022.10:g.38509599T>G , CM000684.1:g.38509599T>G	GRCh37
NC_000022.9:g.36839545T>G	NCBI36
NG_007094.2:g.97099A>C
NG_033059.2:g.2078A>C
NG_007094.3:g.106187A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.2097A>C MANE Select	ENSP00000333142.3:p.Pro699=
ENST00000436218.6:c.*1295A>C	ENSP00000401242.1:n.*1295A>C
ENST00000655142.1:c.*955A>C	ENSP00000499715.1:n.*955A>C
ENST00000660610.1:c.2097A>C	ENSP00000499555.1:p.Pro699=
ENST00000663895.1:c.2097A>C	ENSP00000499712.1:p.Pro699=
ENST00000664587.1:c.1959A>C	ENSP00000499394.1:p.Pro653=
ENST00000665987.1:c.*1836A>C	ENSP00000499423.1:n.*1836A>C
ENST00000667521.1:c.2097A>C	ENSP00000499665.1:p.Pro699=
ENST00000668499.1:c.*1956A>C	ENSP00000499626.1:n.*1956A>C
ENST00000668949.1:c.2139A>C	ENSP00000499711.1:p.Pro713=
ENST00000671093.1:n.2029A>C
ENST00000673413.1:c.*1766A>C	ENSP00000500600.1:n.*1766A>C
ENST00000332509.7:c.2097A>C	ENSP00000333142.3:p.Pro699=
ENST00000335539.7:c.1935A>C	ENSP00000335149.3:p.Pro645=
ENST00000402064.5:c.1935A>C	ENSP00000386100.1:p.Pro645=
ENST00000496409.1:n.805A>C
NM_001004426.1:c.1935A>C	NP_001004426.1:p.Pro645=
NM_001199562.1:c.1935A>C	NP_001186491.1:p.Pro645=
NM_003560.2:c.2097A>C	NP_003551.2:p.Pro699=
XM_005261764.1:c.2097A>C	XP_005261821.1:p.Pro699=
XM_005261765.1:c.2097A>C	XP_005261822.1:p.Pro699=
XM_005261766.1:c.2097A>C	XP_005261823.1:p.Pro699=
XM_006724332.2:c.2097A>C	XP_006724395.1:p.Pro699=
XM_011530422.1:c.1992A>C	XP_011528724.1:p.Pro664=
XM_011530423.1:c.1563A>C	XP_011528725.1:p.Pro521=
XM_011530424.1:c.1563A>C	XP_011528726.1:p.Pro521=
XM_011530425.1:c.1563A>C	XP_011528727.1:p.Pro521=
XR_244390.1:n.2373A>C
XR_430411.1:n.2257A>C
XR_937938.1:n.2459A>C
NM_001004426.2:c.1935A>C	NP_001004426.1:p.Pro645=
NM_001199562.2:c.1935A>C	NP_001186491.1:p.Pro645=
NM_001349864.1:c.2097A>C	NP_001336793.1:p.Pro699=
NM_001349865.1:c.1935A>C	NP_001336794.1:p.Pro645=
NM_001349866.1:c.1935A>C	NP_001336795.1:p.Pro645=
NM_001349867.1:c.1563A>C	NP_001336796.1:p.Pro521=
NM_001349868.1:c.1419A>C	NP_001336797.1:p.Pro473=
NM_001349869.1:c.1401A>C	NP_001336798.1:p.Pro467=
NM_003560.3:c.2097A>C	NP_003551.2:p.Pro699=
XM_005261764.3:c.2097A>C	XP_005261821.1:p.Pro699=
XM_005261765.2:c.2097A>C	XP_005261822.1:p.Pro699=
XM_006724332.4:c.2097A>C	XP_006724395.1:p.Pro699=
XM_017028983.1:c.1401A>C	XP_016884472.1:p.Pro467=
XM_024452280.1:c.1563A>C	XP_024308048.1:p.Pro521=
XM_024452281.1:c.1563A>C	XP_024308049.1:p.Pro521=
XM_024452282.1:c.1563A>C	XP_024308050.1:p.Pro521=
XM_024452283.1:c.1419A>C	XP_024308051.1:p.Pro473=
XM_024452284.1:c.1401A>C	XP_024308052.1:p.Pro467=
XM_024452285.1:c.1401A>C	XP_024308053.1:p.Pro467=
XR_001755325.2:n.2280A>C
XR_001755327.2:n.2275A>C
XR_001755328.2:n.2241A>C
XR_244390.3:n.2357A>C
XR_937938.3:n.2443A>C
NM_001199562.3:c.1935A>C	NP_001186491.1:p.Pro645=
NM_001349864.2:c.2097A>C	NP_001336793.1:p.Pro699=
NM_001349865.2:c.1935A>C	NP_001336794.1:p.Pro645=
NM_001349866.2:c.1935A>C	NP_001336795.1:p.Pro645=
NM_001349867.2:c.1563A>C	NP_001336796.1:p.Pro521=
NM_001349868.2:c.1419A>C	NP_001336797.1:p.Pro473=
NM_001349869.2:c.1401A>C	NP_001336798.1:p.Pro467=
NM_003560.4:c.2097A>C MANE Select	NP_003551.2:p.Pro699=
NM_001004426.3:c.1935A>C	NP_001004426.1:p.Pro645=