Canonical Allele Identifier: CA2404669425

Gene: PLA2G6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38115675_38115676delinsAG , CM000684.2:g.38115675_38115676delinsAG	GRCh38
NC_000022.10:g.38511682_38511683delinsAG , CM000684.1:g.38511682_38511683delinsAG	GRCh37
NC_000022.9:g.36841628_36841629delinsAG	NCBI36
NG_007094.2:g.95015_95016delinsCT
NG_007094.3:g.104103_104104delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.1885_1886delinsCT MANE Select	ENSP00000333142.3:p.Leu629=
ENST00000427114.6:c.1189_1190delinsCT	ENSP00000407743.2:p.Leu397=
ENST00000436218.6:c.*1083_*1084delinsCT	ENSP00000401242.1:n.*1083_*1084delinsCT
ENST00000655142.1:c.*743_*744delinsCT	ENSP00000499715.1:n.*743_*744delinsCT
ENST00000660610.1:c.1885_1886delinsCT	ENSP00000499555.1:p.Leu629=
ENST00000663895.1:c.1885_1886delinsCT	ENSP00000499712.1:p.Leu629=
ENST00000664587.1:c.1747_1748delinsCT	ENSP00000499394.1:p.Leu583=
ENST00000665987.1:c.*1624_*1625delinsCT	ENSP00000499423.1:n.*1624_*1625delinsCT
ENST00000667521.1:c.1885_1886delinsCT	ENSP00000499665.1:p.Leu629=
ENST00000668499.1:c.*1607_*1608delinsCT	ENSP00000499626.1:n.*1607_*1608delinsCT
ENST00000668949.1:c.1723_1724delinsCT	ENSP00000499711.1:p.Leu575=
ENST00000671093.1:n.1817_1818delinsCT
ENST00000673413.1:c.*1554_*1555delinsCT	ENSP00000500600.1:n.*1554_*1555delinsCT
ENST00000332509.7:c.1885_1886delinsCT	ENSP00000333142.3:p.Leu629=
ENST00000335539.7:c.1723_1724delinsCT	ENSP00000335149.3:p.Leu575=
ENST00000402064.5:c.1723_1724delinsCT	ENSP00000386100.1:p.Leu575=
ENST00000454670.1:c.621_622delinsCT
ENST00000496409.1:n.593_594delinsCT
NM_001004426.1:c.1723_1724delinsCT	NP_001004426.1:p.Leu575=
NM_001199562.1:c.1723_1724delinsCT	NP_001186491.1:p.Leu575=
NM_003560.2:c.1885_1886delinsCT	NP_003551.2:p.Leu629=
XM_005261764.1:c.1885_1886delinsCT	XP_005261821.1:p.Leu629=
XM_005261765.1:c.1885_1886delinsCT	XP_005261822.1:p.Leu629=
XM_005261766.1:c.1885_1886delinsCT	XP_005261823.1:p.Leu629=
XM_006724332.2:c.1885_1886delinsCT	XP_006724395.1:p.Leu629=
XM_011530422.1:c.1780_1781delinsCT	XP_011528724.1:p.Leu594=
XM_011530423.1:c.1351_1352delinsCT	XP_011528725.1:p.Leu451=
XM_011530424.1:c.1351_1352delinsCT	XP_011528726.1:p.Leu451=
XM_011530425.1:c.1351_1352delinsCT	XP_011528727.1:p.Leu451=
XR_244390.1:n.2161_2162delinsCT
XR_430411.1:n.2045_2046delinsCT
XR_937937.1:n.2084_2085delinsCT
XR_937938.1:n.2247_2248delinsCT
XR_937939.1:n.2136_2137delinsCT
NM_001004426.2:c.1723_1724delinsCT	NP_001004426.1:p.Leu575=
NM_001199562.2:c.1723_1724delinsCT	NP_001186491.1:p.Leu575=
NM_001349864.1:c.1885_1886delinsCT	NP_001336793.1:p.Leu629=
NM_001349865.1:c.1723_1724delinsCT	NP_001336794.1:p.Leu575=
NM_001349866.1:c.1723_1724delinsCT	NP_001336795.1:p.Leu575=
NM_001349867.1:c.1351_1352delinsCT	NP_001336796.1:p.Leu451=
NM_001349868.1:c.1207_1208delinsCT	NP_001336797.1:p.Leu403=
NM_001349869.1:c.1189_1190delinsCT	NP_001336798.1:p.Leu397=
NM_003560.3:c.1885_1886delinsCT	NP_003551.2:p.Leu629=
XM_005261764.3:c.1885_1886delinsCT	XP_005261821.1:p.Leu629=
XM_005261765.2:c.1885_1886delinsCT	XP_005261822.1:p.Leu629=
XM_006724332.4:c.1885_1886delinsCT	XP_006724395.1:p.Leu629=
XM_017028983.1:c.1189_1190delinsCT	XP_016884472.1:p.Leu397=
XM_024452280.1:c.1351_1352delinsCT	XP_024308048.1:p.Leu451=
XM_024452281.1:c.1351_1352delinsCT	XP_024308049.1:p.Leu451=
XM_024452282.1:c.1351_1352delinsCT	XP_024308050.1:p.Leu451=
XM_024452283.1:c.1207_1208delinsCT	XP_024308051.1:p.Leu403=
XM_024452284.1:c.1189_1190delinsCT	XP_024308052.1:p.Leu397=
XM_024452285.1:c.1189_1190delinsCT	XP_024308053.1:p.Leu397=
XR_001755325.2:n.2068_2069delinsCT
XR_001755327.2:n.2063_2064delinsCT
XR_001755328.2:n.2029_2030delinsCT
XR_244390.3:n.2145_2146delinsCT
XR_937938.3:n.2231_2232delinsCT
XR_937939.3:n.2120_2121delinsCT
NM_001199562.3:c.1723_1724delinsCT	NP_001186491.1:p.Leu575=
NM_001349864.2:c.1885_1886delinsCT	NP_001336793.1:p.Leu629=
NM_001349865.2:c.1723_1724delinsCT	NP_001336794.1:p.Leu575=
NM_001349866.2:c.1723_1724delinsCT	NP_001336795.1:p.Leu575=
NM_001349867.2:c.1351_1352delinsCT	NP_001336796.1:p.Leu451=
NM_001349868.2:c.1207_1208delinsCT	NP_001336797.1:p.Leu403=
NM_001349869.2:c.1189_1190delinsCT	NP_001336798.1:p.Leu397=
NM_003560.4:c.1885_1886delinsCT MANE Select	NP_003551.2:p.Leu629=
NM_001004426.3:c.1723_1724delinsCT	NP_001004426.1:p.Leu575=