Canonical Allele Identifier: CA2404668388
Community Standard Title: NM_003560.4(PLA2G6):c.2098C= (p.Gln700=)
Gene: PLA2G6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38113591G= , CM000684.2:g.38113591G= GRCh38
NC_000022.10:g.38509598G= , CM000684.1:g.38509598G= GRCh37
NC_000022.9:g.36839544G= NCBI36
NG_007094.2:g.97100C=
NG_033059.2:g.2079C=
NG_007094.3:g.106188C=

Transcript Alleles

HGVS Amino-acid Change
NM_003560.4:c.2098C= MANE Select NP_003551.2:p.Gln700=
ENST00000332509.8:c.2098C= MANE Select ENSP00000333142.3:p.Gln700=
NM_001004426.1:c.1936C= NP_001004426.1:p.Gln646=
NM_001004426.2:c.1936C= NP_001004426.1:p.Gln646=
NM_001004426.3:c.1936C= NP_001004426.1:p.Gln646=
NM_001199562.1:c.1936C= NP_001186491.1:p.Gln646=
NM_001199562.2:c.1936C= NP_001186491.1:p.Gln646=
NM_001199562.3:c.1936C= NP_001186491.1:p.Gln646=
NM_001349864.1:c.2098C= NP_001336793.1:p.Gln700=
NM_001349864.2:c.2098C= NP_001336793.1:p.Gln700=
NM_001349865.1:c.1936C= NP_001336794.1:p.Gln646=
NM_001349865.2:c.1936C= NP_001336794.1:p.Gln646=
NM_001349866.1:c.1936C= NP_001336795.1:p.Gln646=
NM_001349866.2:c.1936C= NP_001336795.1:p.Gln646=
NM_001349867.1:c.1564C= NP_001336796.1:p.Gln522=
NM_001349867.2:c.1564C= NP_001336796.1:p.Gln522=
NM_001349868.1:c.1420C= NP_001336797.1:p.Gln474=
NM_001349868.2:c.1420C= NP_001336797.1:p.Gln474=
NM_001349869.1:c.1402C= NP_001336798.1:p.Gln468=
NM_001349869.2:c.1402C= NP_001336798.1:p.Gln468=
NM_003560.2:c.2098C= NP_003551.2:p.Gln700=
NM_003560.3:c.2098C= NP_003551.2:p.Gln700=
ENST00000332509.7:c.2098C= ENSP00000333142.3:p.Gln700=
ENST00000335539.7:c.1936C= ENSP00000335149.3:p.Gln646=
ENST00000402064.5:c.1936C= ENSP00000386100.1:p.Gln646=
ENST00000436218.6:c.*1296C= ENSP00000401242.1:n.*1296C=
ENST00000496409.1:n.806C=
ENST00000655142.1:c.*956C= ENSP00000499715.1:n.*956C=
ENST00000660610.1:c.2098C= ENSP00000499555.1:p.Gln700=
ENST00000663895.1:c.2098C= ENSP00000499712.1:p.Gln700=
ENST00000664587.1:c.1960C= ENSP00000499394.1:p.Gln654=
ENST00000665987.1:c.*1837C= ENSP00000499423.1:n.*1837C=
ENST00000667521.1:c.2098C= ENSP00000499665.1:p.Gln700=
ENST00000668499.1:c.*1957C= ENSP00000499626.1:n.*1957C=
ENST00000668949.1:c.2140C= ENSP00000499711.1:p.Gln714=
ENST00000671093.1:n.2030C=
ENST00000673413.1:c.*1767C= ENSP00000500600.1:n.*1767C=
XM_005261764.1:c.2098C= XP_005261821.1:p.Gln700=
XM_005261764.3:c.2098C= XP_005261821.1:p.Gln700=
XM_005261765.1:c.2098C= XP_005261822.1:p.Gln700=
XM_005261765.2:c.2098C= XP_005261822.1:p.Gln700=
XM_005261766.1:c.2098C= XP_005261823.1:p.Gln700=
XM_006724332.2:c.2098C= XP_006724395.1:p.Gln700=
XM_006724332.4:c.2098C= XP_006724395.1:p.Gln700=
XM_011530422.1:c.1993C= XP_011528724.1:p.Gln665=
XM_011530423.1:c.1564C= XP_011528725.1:p.Gln522=
XM_011530424.1:c.1564C= XP_011528726.1:p.Gln522=
XM_011530425.1:c.1564C= XP_011528727.1:p.Gln522=
XM_017028983.1:c.1402C= XP_016884472.1:p.Gln468=
XM_024452280.1:c.1564C= XP_024308048.1:p.Gln522=
XM_024452281.1:c.1564C= XP_024308049.1:p.Gln522=
XM_024452282.1:c.1564C= XP_024308050.1:p.Gln522=
XM_024452283.1:c.1420C= XP_024308051.1:p.Gln474=
XM_024452284.1:c.1402C= XP_024308052.1:p.Gln468=
XM_024452285.1:c.1402C= XP_024308053.1:p.Gln468=
XR_001755325.2:n.2281C=
XR_001755327.2:n.2276C=
XR_001755328.2:n.2242C=
XR_244390.1:n.2374C=
XR_244390.3:n.2358C=
XR_430411.1:n.2258C=
XR_937938.1:n.2460C=
XR_937938.3:n.2444C=