Canonical Allele Identifier: CA2404667626
Gene: PLA2G6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38112143G= , CM000684.2:g.38112143G= GRCh38
NC_000022.10:g.38508150G= , CM000684.1:g.38508150G= GRCh37
NC_000022.9:g.36838096G= NCBI36
NG_007094.2:g.98548C=
NG_033059.2:g.3527C=
NG_007094.3:g.107636C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332509.8:c.*18C= MANE Select ENSP00000333142.3:n.*18C=
ENST00000655142.1:c.*1297C= ENSP00000499715.1:n.*1297C=
ENST00000660610.1:c.*18C= ENSP00000499555.1:n.*18C=
ENST00000663895.1:c.*18C= ENSP00000499712.1:n.*18C=
ENST00000664587.1:c.*18C= ENSP00000499394.1:n.*18C=
ENST00000665987.1:c.*2178C= ENSP00000499423.1:n.*2178C=
ENST00000667521.1:c.*18C= ENSP00000499665.1:n.*18C=
ENST00000668499.1:c.*2298C= ENSP00000499626.1:n.*2298C=
ENST00000668949.1:c.*18C= ENSP00000499711.1:n.*18C=
ENST00000671093.1:n.2371C=
ENST00000673413.1:c.*2108C= ENSP00000500600.1:n.*2108C=
ENST00000332509.7:c.*18C= ENSP00000333142.3:n.*18C=
ENST00000335539.7:c.*18C= ENSP00000335149.3:n.*18C=
ENST00000402064.5:c.*18C= ENSP00000386100.1:n.*18C=
ENST00000463287.1:n.515C=
NM_001004426.1:c.*18C= NP_001004426.1:n.*18C=
NM_001199562.1:c.*18C= NP_001186491.1:n.*18C=
NM_003560.2:c.*18C= NP_003551.2:n.*18C=
XM_005261764.1:c.*18C= XP_005261821.1:n.*18C=
XM_005261765.1:c.*18C= XP_005261822.1:n.*18C=
XM_005261766.1:c.*18C= XP_005261823.1:n.*18C=
XM_006724332.2:c.*18C= XP_006724395.1:n.*18C=
XM_011530422.1:c.*18C= XP_011528724.1:n.*18C=
XM_011530423.1:c.*18C= XP_011528725.1:n.*18C=
XM_011530424.1:c.*18C= XP_011528726.1:n.*18C=
XM_011530425.1:c.*18C= XP_011528727.1:n.*18C=
NM_001004426.2:c.*18C= NP_001004426.1:n.*18C=
NM_001199562.2:c.*18C= NP_001186491.1:n.*18C=
NM_001349864.1:c.*18C= NP_001336793.1:n.*18C=
NM_001349865.1:c.*18C= NP_001336794.1:n.*18C=
NM_001349866.1:c.*18C= NP_001336795.1:n.*18C=
NM_001349867.1:c.*18C= NP_001336796.1:n.*18C=
NM_001349868.1:c.*18C= NP_001336797.1:n.*18C=
NM_001349869.1:c.*18C= NP_001336798.1:n.*18C=
NM_003560.3:c.*18C= NP_003551.2:n.*18C=
XM_005261764.3:c.*18C= XP_005261821.1:n.*18C=
XM_005261765.2:c.*18C= XP_005261822.1:n.*18C=
XM_006724332.4:c.*18C= XP_006724395.1:n.*18C=
XM_017028983.1:c.*18C= XP_016884472.1:n.*18C=
XM_024452280.1:c.*18C= XP_024308048.1:n.*18C=
XM_024452281.1:c.*18C= XP_024308049.1:n.*18C=
XM_024452282.1:c.*18C= XP_024308050.1:n.*18C=
XM_024452283.1:c.*18C= XP_024308051.1:n.*18C=
XM_024452284.1:c.*18C= XP_024308052.1:n.*18C=
XM_024452285.1:c.*18C= XP_024308053.1:n.*18C=
XR_001755325.2:n.2622C=
XR_001755327.2:n.2617C=
XR_001755328.2:n.2583C=
NM_001199562.3:c.*18C= NP_001186491.1:n.*18C=
NM_001349864.2:c.*18C= NP_001336793.1:n.*18C=
NM_001349865.2:c.*18C= NP_001336794.1:n.*18C=
NM_001349866.2:c.*18C= NP_001336795.1:n.*18C=
NM_001349867.2:c.*18C= NP_001336796.1:n.*18C=
NM_001349868.2:c.*18C= NP_001336797.1:n.*18C=
NM_001349869.2:c.*18C= NP_001336798.1:n.*18C=
NM_003560.4:c.*18C= MANE Select NP_003551.2:n.*18C=
NM_001004426.3:c.*18C= NP_001004426.1:n.*18C=