Canonical Allele Identifier: CA2656638101

Gene: PLA2G6

Linked Data

• gnomAD v4: 22-38115422-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38115425_38115426del , CM000684.2:g.38115425_38115426del	GRCh38
NC_000022.10:g.38511432_38511433del , CM000684.1:g.38511432_38511433del	GRCh37
NC_000022.9:g.36841378_36841379del	NCBI36
NG_007094.2:g.95267_95268del
NG_033059.2:g.246_247del
NG_007094.3:g.104355_104356del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.2034+103_2034+104del MANE Select	ENSP00000333142.3:n.2034+103_2034+104del
ENST00000436218.6:c.*1232+103_*1232+104del	ENSP00000401242.1:n.*1232+103_*1232+104del
ENST00000655142.1:c.*892+103_*892+104del	ENSP00000499715.1:n.*892+103_*892+104del
ENST00000660610.1:c.2034+103_2034+104del	ENSP00000499555.1:n.2034+103_2034+104del
ENST00000663895.1:c.2034+103_2034+104del	ENSP00000499712.1:n.2034+103_2034+104del
ENST00000664587.1:c.1896+103_1896+104del	ENSP00000499394.1:n.1896+103_1896+104del
ENST00000665987.1:c.*1773+103_*1773+104del	ENSP00000499423.1:n.*1773+103_*1773+104del
ENST00000667521.1:c.2034+103_2034+104del	ENSP00000499665.1:n.2034+103_2034+104del
ENST00000668499.1:c.*1756+103_*1756+104del	ENSP00000499626.1:n.*1756+103_*1756+104del
ENST00000668949.1:c.1872+103_1872+104del	ENSP00000499711.1:n.1872+103_1872+104del
ENST00000671093.1:n.1966+103_1966+104del
ENST00000673413.1:c.*1703+103_*1703+104del	ENSP00000500600.1:n.*1703+103_*1703+104del
ENST00000332509.7:c.2034+103_2034+104del	ENSP00000333142.3:n.2034+103_2034+104del
ENST00000335539.7:c.1872+103_1872+104del	ENSP00000335149.3:n.1872+103_1872+104del
ENST00000402064.5:c.1872+103_1872+104del	ENSP00000386100.1:n.1872+103_1872+104del
ENST00000496409.1:n.742+103_742+104del
NM_001004426.1:c.1872+103_1872+104del	NP_001004426.1:n.1872+103_1872+104del
NM_001199562.1:c.1872+103_1872+104del	NP_001186491.1:n.1872+103_1872+104del
NM_003560.2:c.2034+103_2034+104del	NP_003551.2:n.2034+103_2034+104del
XM_005261764.1:c.2034+103_2034+104del	XP_005261821.1:n.2034+103_2034+104del
XM_005261765.1:c.2034+103_2034+104del	XP_005261822.1:n.2034+103_2034+104del
XM_005261766.1:c.2034+103_2034+104del	XP_005261823.1:n.2034+103_2034+104del
XM_006724332.2:c.2034+103_2034+104del	XP_006724395.1:n.2034+103_2034+104del
XM_011530422.1:c.1929+103_1929+104del	XP_011528724.1:n.1929+103_1929+104del
XM_011530423.1:c.1500+103_1500+104del	XP_011528725.1:n.1500+103_1500+104del
XM_011530424.1:c.1500+103_1500+104del	XP_011528726.1:n.1500+103_1500+104del
XM_011530425.1:c.1500+103_1500+104del	XP_011528727.1:n.1500+103_1500+104del
XR_244390.1:n.2310+103_2310+104del
XR_430411.1:n.2194+103_2194+104del
XR_937938.1:n.2396+103_2396+104del
NM_001004426.2:c.1872+103_1872+104del	NP_001004426.1:n.1872+103_1872+104del
NM_001199562.2:c.1872+103_1872+104del	NP_001186491.1:n.1872+103_1872+104del
NM_001349864.1:c.2034+103_2034+104del	NP_001336793.1:n.2034+103_2034+104del
NM_001349865.1:c.1872+103_1872+104del	NP_001336794.1:n.1872+103_1872+104del
NM_001349866.1:c.1872+103_1872+104del	NP_001336795.1:n.1872+103_1872+104del
NM_001349867.1:c.1500+103_1500+104del	NP_001336796.1:n.1500+103_1500+104del
NM_001349868.1:c.1356+103_1356+104del	NP_001336797.1:n.1356+103_1356+104del
NM_001349869.1:c.1338+103_1338+104del	NP_001336798.1:n.1338+103_1338+104del
NM_003560.3:c.2034+103_2034+104del	NP_003551.2:n.2034+103_2034+104del
XM_005261764.3:c.2034+103_2034+104del	XP_005261821.1:n.2034+103_2034+104del
XM_005261765.2:c.2034+103_2034+104del	XP_005261822.1:n.2034+103_2034+104del
XM_006724332.4:c.2034+103_2034+104del	XP_006724395.1:n.2034+103_2034+104del
XM_017028983.1:c.1338+103_1338+104del	XP_016884472.1:n.1338+103_1338+104del
XM_024452280.1:c.1500+103_1500+104del	XP_024308048.1:n.1500+103_1500+104del
XM_024452281.1:c.1500+103_1500+104del	XP_024308049.1:n.1500+103_1500+104del
XM_024452282.1:c.1500+103_1500+104del	XP_024308050.1:n.1500+103_1500+104del
XM_024452283.1:c.1356+103_1356+104del	XP_024308051.1:n.1356+103_1356+104del
XM_024452284.1:c.1338+103_1338+104del	XP_024308052.1:n.1338+103_1338+104del
XM_024452285.1:c.1338+103_1338+104del	XP_024308053.1:n.1338+103_1338+104del
XR_001755325.2:n.2217+103_2217+104del
XR_001755327.2:n.2212+103_2212+104del
XR_001755328.2:n.2178+103_2178+104del
XR_244390.3:n.2294+103_2294+104del
XR_937938.3:n.2380+103_2380+104del
NM_001199562.3:c.1872+103_1872+104del	NP_001186491.1:n.1872+103_1872+104del
NM_001349864.2:c.2034+103_2034+104del	NP_001336793.1:n.2034+103_2034+104del
NM_001349865.2:c.1872+103_1872+104del	NP_001336794.1:n.1872+103_1872+104del
NM_001349866.2:c.1872+103_1872+104del	NP_001336795.1:n.1872+103_1872+104del
NM_001349867.2:c.1500+103_1500+104del	NP_001336796.1:n.1500+103_1500+104del
NM_001349868.2:c.1356+103_1356+104del	NP_001336797.1:n.1356+103_1356+104del
NM_001349869.2:c.1338+103_1338+104del	NP_001336798.1:n.1338+103_1338+104del
NM_003560.4:c.2034+103_2034+104del MANE Select	NP_003551.2:n.2034+103_2034+104del
NM_001004426.3:c.1872+103_1872+104del	NP_001004426.1:n.1872+103_1872+104del