Canonical Allele Identifier: CA173295
Gene: PLA2G6 HGNC NCBI

Linked Data

ClinVar Variation Id: 159781
dbSNP Id: rs2267369

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38169340C>T , CM000684.2:g.38169340C>T GRCh38
NC_000022.10:g.38565347C>T , CM000684.1:g.38565347C>T GRCh37
NC_000022.9:g.36895293C>T NCBI36
NG_007094.2:g.41351G>A
NG_007094.3:g.50439G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000332509.8:c.87G>A MANE Select ENSP00000333142.3:p.Val29=
ENST00000436218.6:c.87G>A ENSP00000401242.1:p.Val29=
ENST00000655142.1:c.87G>A ENSP00000499715.1:p.Val29=
ENST00000660610.1:c.87G>A ENSP00000499555.1:p.Val29=
ENST00000663895.1:c.87G>A ENSP00000499712.1:p.Val29=
ENST00000664587.1:c.87G>A ENSP00000499394.1:p.Val29=
ENST00000665987.1:c.87G>A ENSP00000499423.1:p.Val29=
ENST00000667521.1:c.87G>A ENSP00000499665.1:p.Val29=
ENST00000668208.1:n.217G>A
ENST00000668499.1:c.87G>A ENSP00000499626.1:p.Val29=
ENST00000668949.1:c.87G>A ENSP00000499711.1:p.Val29=
ENST00000673413.1:c.87G>A ENSP00000500600.1:p.Val29=
ENST00000332509.7:c.87G>A ENSP00000333142.3:p.Val29=
ENST00000335539.7:c.87G>A ENSP00000335149.3:p.Val29=
ENST00000402064.5:c.87G>A ENSP00000386100.1:p.Val29=
ENST00000417303.6:c.87G>A ENSP00000404974.2:p.Val29=
ENST00000420435.5:n.178G>A
ENST00000426674.1:n.252G>A
ENST00000430886.5:c.87G>A ENSP00000395464.1:p.Val29=
ENST00000435484.5:c.87G>A ENSP00000413597.1:p.Val29=
ENST00000436218.5:c.87G>A ENSP00000401242.1:p.Val29=
ENST00000447598.6:c.87G>A ENSP00000393361.2:p.Val29=
ENST00000455341.2:c.87G>A ENSP00000393761.2:p.Val29=
ENST00000471636.5:n.163G>A
ENST00000594306.1:c.87G>A ENSP00000473160.1:p.Val29=
NM_001004426.1:c.87G>A NP_001004426.1:p.Val29=
NM_001199562.1:c.87G>A NP_001186491.1:p.Val29=
NM_003560.2:c.87G>A NP_003551.2:p.Val29=
XM_005261764.1:c.87G>A XP_005261821.1:p.Val29=
XM_005261765.1:c.87G>A XP_005261822.1:p.Val29=
XM_005261766.1:c.87G>A XP_005261823.1:p.Val29=
XM_005261771.3:c.87G>A XP_005261828.1:p.Val29=
XM_006724332.2:c.87G>A XP_006724395.1:p.Val29=
XM_011530422.1:c.87G>A XP_011528724.1:p.Val29=
XM_011530423.1:c.-579G>A XP_011528725.1:n.-579G>A
XM_011530424.1:c.-705G>A XP_011528726.1:n.-705G>A
XM_011530426.1:c.87G>A XP_011528728.1:p.Val29=
XM_011530427.1:c.87G>A XP_011528729.1:p.Val29=
XM_011530428.1:c.87G>A XP_011528730.1:p.Val29=
XR_244390.1:n.195G>A
XR_244392.1:n.195G>A
XR_430411.1:n.195G>A
XR_430412.1:n.195G>A
XR_937937.1:n.195G>A
XR_937938.1:n.195G>A
XR_937939.1:n.195G>A
XR_937940.1:n.195G>A
NM_001004426.2:c.87G>A NP_001004426.1:p.Val29=
NM_001199562.2:c.87G>A NP_001186491.1:p.Val29=
NM_001349864.1:c.87G>A NP_001336793.1:p.Val29=
NM_001349865.1:c.87G>A NP_001336794.1:p.Val29=
NM_001349866.1:c.87G>A NP_001336795.1:p.Val29=
NM_001349867.1:c.-579G>A NP_001336796.1:n.-579G>A
NM_001349868.1:c.-404G>A NP_001336797.1:n.-404G>A
NM_001349869.1:c.-579G>A NP_001336798.1:n.-579G>A
NM_003560.3:c.87G>A NP_003551.2:p.Val29=
XM_005261764.3:c.87G>A XP_005261821.1:p.Val29=
XM_005261765.2:c.87G>A XP_005261822.1:p.Val29=
XM_006724332.4:c.87G>A XP_006724395.1:p.Val29=
XM_011530426.3:c.87G>A XP_011528728.1:p.Val29=
XM_017028983.1:c.-705G>A XP_016884472.1:n.-705G>A
XM_017028986.2:c.87G>A XP_016884475.1:p.Val29=
XM_017028987.2:c.87G>A XP_016884476.1:p.Val29=
XM_017028988.2:c.87G>A XP_016884477.1:p.Val29=
XM_024452280.1:c.-579G>A XP_024308048.1:n.-579G>A
XM_024452281.1:c.-574G>A XP_024308049.1:n.-574G>A
XM_024452283.1:c.-404G>A XP_024308051.1:n.-404G>A
XM_024452284.1:c.-579G>A XP_024308052.1:n.-579G>A
XM_024452285.1:c.-574G>A XP_024308053.1:n.-574G>A
XR_001755325.2:n.179G>A
XR_001755327.2:n.179G>A
XR_001755328.2:n.179G>A
XR_244390.3:n.179G>A
XR_937938.3:n.179G>A
XR_937939.3:n.179G>A
XR_937940.3:n.179G>A
NM_001199562.3:c.87G>A NP_001186491.1:p.Val29=
NM_001349864.2:c.87G>A NP_001336793.1:p.Val29=
NM_001349865.2:c.87G>A NP_001336794.1:p.Val29=
NM_001349866.2:c.87G>A NP_001336795.1:p.Val29=
NM_001349867.2:c.-579G>A NP_001336796.1:n.-579G>A
NM_001349868.2:c.-404G>A NP_001336797.1:n.-404G>A
NM_001349869.2:c.-579G>A NP_001336798.1:n.-579G>A
NM_003560.4:c.87G>A MANE Select NP_003551.2:p.Val29=
NM_001004426.3:c.87G>A NP_001004426.1:p.Val29=