Canonical Allele Identifier: CA2128340
Gene: GMPPA HGNC NCBI
ASIC4-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219505755G>A , CM000664.2:g.219505755G>A GRCh38
NC_000002.11:g.220370477G>A , CM000664.1:g.220370477G>A GRCh37
NC_000002.10:g.220078721G>A NCBI36
NG_033833.1:g.11891G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000341142.8:c.894G>A (GMPPA) ENSP00000340760.3:p.Ser298=
ENST00000455657.6:c.*169G>A (GMPPA) ENSP00000392465.3:n.*169G>A
ENST00000496536.2:n.903G>A (GMPPA)
ENST00000622191.2:c.894G>A (GMPPA) ENSP00000478700.2:p.Ser298=
ENST00000682058.1:c.*925G>A (GMPPA) ENSP00000507378.1:n.*925G>A
ENST00000682102.1:c.*134G>A (GMPPA) ENSP00000508279.1:n.*134G>A
ENST00000682340.1:n.2527G>A (GMPPA)
ENST00000682435.1:n.1498G>A (GMPPA)
ENST00000682443.1:n.2180G>A (GMPPA)
ENST00000682481.1:c.*1179G>A (GMPPA) ENSP00000507331.1:n.*1179G>A
ENST00000682488.1:c.70-969G>A (GMPPA) ENSP00000507140.1:n.70-969G>A
ENST00000682576.1:c.*942G>A (GMPPA) ENSP00000508370.1:n.*942G>A
ENST00000683106.1:n.2073G>A (GMPPA)
ENST00000683131.1:c.*1179G>A (GMPPA) ENSP00000507530.1:n.*1179G>A
ENST00000683241.1:n.1279G>A (GMPPA)
ENST00000683382.1:n.2156G>A (GMPPA)
ENST00000683386.1:c.*524G>A (GMPPA) ENSP00000507844.1:n.*524G>A
ENST00000683402.1:c.*275G>A (GMPPA) ENSP00000507137.1:n.*275G>A
ENST00000683591.1:c.*925G>A (GMPPA) ENSP00000508406.1:n.*925G>A
ENST00000683598.1:c.*925G>A (GMPPA) ENSP00000508168.1:n.*925G>A
ENST00000683617.1:n.2012G>A (GMPPA)
ENST00000683626.1:c.*1538G>A (GMPPA) ENSP00000507216.1:n.*1538G>A
ENST00000683691.1:c.*805G>A (GMPPA) ENSP00000508392.1:n.*805G>A
ENST00000683746.1:n.1844G>A (GMPPA)
ENST00000683752.1:c.543G>A (GMPPA) ENSP00000507197.1:p.Ser181=
ENST00000683864.1:c.*1674G>A (GMPPA) ENSP00000507147.1:n.*1674G>A
ENST00000683946.1:c.894G>A (GMPPA) ENSP00000506941.1:p.Ser298=
ENST00000684227.1:c.*945G>A (GMPPA) ENSP00000507190.1:n.*945G>A
ENST00000684242.1:n.1949G>A (GMPPA)
ENST00000684274.1:n.1264G>A (GMPPA)
ENST00000684334.1:n.2138G>A (GMPPA)
ENST00000684412.1:n.1399G>A (GMPPA)
ENST00000684562.1:n.1934G>A (GMPPA)
ENST00000684706.1:n.958G>A (GMPPA)
ENST00000684729.1:c.*945G>A (GMPPA) ENSP00000507441.1:n.*945G>A
ENST00000313597.10:c.894G>A (GMPPA) MANE Select ENSP00000315925.6:p.Ser298=
ENST00000313597.9:c.894G>A (GMPPA) ENSP00000315925.5:p.Ser298=
ENST00000341142.7:c.894G>A (GMPPA) ENSP00000340760.3:p.Ser298=
ENST00000358215.8:c.894G>A (GMPPA) ENSP00000350949.3:p.Ser298=
ENST00000373908.5:c.894G>A (GMPPA) ENSP00000363016.1:p.Ser298=
ENST00000373917.7:c.1053G>A (GMPPA) ENSP00000363027.3:p.Ser351=
ENST00000443704.5:c.*41G>A (GMPPA) ENSP00000396750.1:n.*41G>A
ENST00000480034.1:c.31G>A (GMPPA)
ENST00000481170.1:n.3891G>A (GMPPA)
ENST00000622191.1:c.894G>A (GMPPA) ENSP00000478700.1:p.Ser298=
NM_013335.3:c.894G>A (GMPPA) NP_037467.2:p.Ser298=
NM_205847.2:c.894G>A (GMPPA) NP_995319.1:p.Ser298=
XM_005246483.2:c.909G>A (GMPPA) XP_005246540.1:p.Ser303=
XM_005246485.2:c.909G>A (GMPPA) XP_005246542.1:p.Ser303=
XM_005246486.2:c.894G>A (GMPPA) XP_005246543.1:p.Ser298=
XM_011511032.1:c.909G>A (GMPPA) XP_011509334.1:p.Ser303=
XM_011511033.1:c.534G>A (GMPPA) XP_011509335.1:p.Ser178=
XM_011511034.1:c.*41G>A (GMPPA) XP_011509336.1:n.*41G>A
XR_241307.2:n.1008G>A (GMPPA)
XR_923921.1:n.352+10941C>T (ASIC4-AS1)
XM_005246486.3:c.894G>A (GMPPA) XP_005246543.1:p.Ser298=
XM_024452823.1:c.894G>A (GMPPA) XP_024308591.1:p.Ser298=
XR_923921.2:n.391+10941C>T (ASIC4-AS1)
NM_001374294.1:c.894G>A (GMPPA) NP_001361223.1:p.Ser298=
NM_001374295.1:c.894G>A (GMPPA) NP_001361224.1:p.Ser298=
NM_013335.4:c.894G>A (GMPPA) MANE Select NP_037467.2:p.Ser298=
NM_205847.3:c.894G>A (GMPPA) NP_995319.1:p.Ser298=