Canonical Allele Identifier: CA2656633769

Gene: PLA2G6

Linked Data

• gnomAD v4: 22-38112370-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38112370G>C , CM000684.2:g.38112370G>C	GRCh38
NC_000022.10:g.38508377G>C , CM000684.1:g.38508377G>C	GRCh37
NC_000022.9:g.36838323G>C	NCBI36
NG_007094.2:g.98321C>G
NG_033059.2:g.3300C>G
NG_007094.3:g.107409C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.2277-65C>G MANE Select	ENSP00000333142.3:n.2277-65C>G
ENST00000436218.6:c.*1475-65C>G	ENSP00000401242.1:n.*1475-65C>G
ENST00000655142.1:c.*1135-65C>G	ENSP00000499715.1:n.*1135-65C>G
ENST00000660610.1:c.2277-65C>G	ENSP00000499555.1:n.2277-65C>G
ENST00000663895.1:c.2277-65C>G	ENSP00000499712.1:n.2277-65C>G
ENST00000664587.1:c.2139-65C>G	ENSP00000499394.1:n.2139-65C>G
ENST00000665987.1:c.*2016-65C>G	ENSP00000499423.1:n.*2016-65C>G
ENST00000667521.1:c.2277-65C>G	ENSP00000499665.1:n.2277-65C>G
ENST00000668499.1:c.*2136-65C>G	ENSP00000499626.1:n.*2136-65C>G
ENST00000668949.1:c.2319-65C>G	ENSP00000499711.1:n.2319-65C>G
ENST00000671093.1:n.2209-65C>G
ENST00000673413.1:c.*1946-65C>G	ENSP00000500600.1:n.*1946-65C>G
ENST00000332509.7:c.2277-65C>G	ENSP00000333142.3:n.2277-65C>G
ENST00000335539.7:c.2115-65C>G	ENSP00000335149.3:n.2115-65C>G
ENST00000402064.5:c.2115-65C>G	ENSP00000386100.1:n.2115-65C>G
ENST00000463287.1:n.353-65C>G
NM_001004426.1:c.2115-65C>G	NP_001004426.1:n.2115-65C>G
NM_001199562.1:c.2115-65C>G	NP_001186491.1:n.2115-65C>G
NM_003560.2:c.2277-65C>G	NP_003551.2:n.2277-65C>G
XM_005261764.1:c.2277-65C>G	XP_005261821.1:n.2277-65C>G
XM_005261765.1:c.2277-65C>G	XP_005261822.1:n.2277-65C>G
XM_005261766.1:c.2277-65C>G	XP_005261823.1:n.2277-65C>G
XM_006724332.2:c.2277-65C>G	XP_006724395.1:n.2277-65C>G
XM_011530422.1:c.2172-65C>G	XP_011528724.1:n.2172-65C>G
XM_011530423.1:c.1743-65C>G	XP_011528725.1:n.1743-65C>G
XM_011530424.1:c.1743-65C>G	XP_011528726.1:n.1743-65C>G
XM_011530425.1:c.1743-65C>G	XP_011528727.1:n.1743-65C>G
NM_001004426.2:c.2115-65C>G	NP_001004426.1:n.2115-65C>G
NM_001199562.2:c.2115-65C>G	NP_001186491.1:n.2115-65C>G
NM_001349864.1:c.2277-65C>G	NP_001336793.1:n.2277-65C>G
NM_001349865.1:c.2115-65C>G	NP_001336794.1:n.2115-65C>G
NM_001349866.1:c.2115-65C>G	NP_001336795.1:n.2115-65C>G
NM_001349867.1:c.1743-65C>G	NP_001336796.1:n.1743-65C>G
NM_001349868.1:c.1599-65C>G	NP_001336797.1:n.1599-65C>G
NM_001349869.1:c.1581-65C>G	NP_001336798.1:n.1581-65C>G
NM_003560.3:c.2277-65C>G	NP_003551.2:n.2277-65C>G
XM_005261764.3:c.2277-65C>G	XP_005261821.1:n.2277-65C>G
XM_005261765.2:c.2277-65C>G	XP_005261822.1:n.2277-65C>G
XM_006724332.4:c.2277-65C>G	XP_006724395.1:n.2277-65C>G
XM_017028983.1:c.1581-65C>G	XP_016884472.1:n.1581-65C>G
XM_024452280.1:c.1743-65C>G	XP_024308048.1:n.1743-65C>G
XM_024452281.1:c.1743-65C>G	XP_024308049.1:n.1743-65C>G
XM_024452282.1:c.1743-65C>G	XP_024308050.1:n.1743-65C>G
XM_024452283.1:c.1599-65C>G	XP_024308051.1:n.1599-65C>G
XM_024452284.1:c.1581-65C>G	XP_024308052.1:n.1581-65C>G
XM_024452285.1:c.1581-65C>G	XP_024308053.1:n.1581-65C>G
XR_001755325.2:n.2460-65C>G
XR_001755327.2:n.2455-65C>G
XR_001755328.2:n.2421-65C>G
NM_001199562.3:c.2115-65C>G	NP_001186491.1:n.2115-65C>G
NM_001349864.2:c.2277-65C>G	NP_001336793.1:n.2277-65C>G
NM_001349865.2:c.2115-65C>G	NP_001336794.1:n.2115-65C>G
NM_001349866.2:c.2115-65C>G	NP_001336795.1:n.2115-65C>G
NM_001349867.2:c.1743-65C>G	NP_001336796.1:n.1743-65C>G
NM_001349868.2:c.1599-65C>G	NP_001336797.1:n.1599-65C>G
NM_001349869.2:c.1581-65C>G	NP_001336798.1:n.1581-65C>G
NM_003560.4:c.2277-65C>G MANE Select	NP_003551.2:n.2277-65C>G
NM_001004426.3:c.2115-65C>G	NP_001004426.1:n.2115-65C>G