Canonical Allele Identifier: CA2128282
Gene: GMPPA HGNC NCBI
ASIC4-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219505448C>T , CM000664.2:g.219505448C>T GRCh38
NC_000002.11:g.220370170C>T , CM000664.1:g.220370170C>T GRCh37
NC_000002.10:g.220078414C>T NCBI36
NG_033833.1:g.11584C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000341142.8:c.756-10C>T (GMPPA) ENSP00000340760.3:n.756-10C>T
ENST00000435316.6:c.651-10C>T (GMPPA) ENSP00000411060.1:n.651-10C>T
ENST00000455657.6:c.*31-10C>T (GMPPA) ENSP00000392465.3:n.*31-10C>T
ENST00000496536.2:n.765-10C>T (GMPPA)
ENST00000622191.2:c.756-10C>T (GMPPA) ENSP00000478700.2:n.756-10C>T
ENST00000682058.1:c.*787-10C>T (GMPPA) ENSP00000507378.1:n.*787-10C>T
ENST00000682102.1:c.755+86C>T (GMPPA) ENSP00000508279.1:n.755+86C>T
ENST00000682340.1:n.2220C>T (GMPPA)
ENST00000682435.1:n.1340-10C>T (GMPPA)
ENST00000682443.1:n.2042-10C>T (GMPPA)
ENST00000682481.1:c.*1041-10C>T (GMPPA) ENSP00000507331.1:n.*1041-10C>T
ENST00000682488.1:c.70-1276C>T (GMPPA) ENSP00000507140.1:n.70-1276C>T
ENST00000682576.1:c.*786+86C>T (GMPPA) ENSP00000508370.1:n.*786+86C>T
ENST00000683106.1:n.1776-10C>T (GMPPA)
ENST00000683131.1:c.*1041-10C>T (GMPPA) ENSP00000507530.1:n.*1041-10C>T
ENST00000683241.1:n.1121-10C>T (GMPPA)
ENST00000683382.1:n.1859-10C>T (GMPPA)
ENST00000683386.1:c.*386-10C>T (GMPPA) ENSP00000507844.1:n.*386-10C>T
ENST00000683402.1:c.*137-10C>T (GMPPA) ENSP00000507137.1:n.*137-10C>T
ENST00000683591.1:c.*787-10C>T (GMPPA) ENSP00000508406.1:n.*787-10C>T
ENST00000683598.1:c.*787-10C>T (GMPPA) ENSP00000508168.1:n.*787-10C>T
ENST00000683617.1:n.1856+86C>T (GMPPA)
ENST00000683626.1:c.*1400-10C>T (GMPPA) ENSP00000507216.1:n.*1400-10C>T
ENST00000683691.1:c.*647-10C>T (GMPPA) ENSP00000508392.1:n.*647-10C>T
ENST00000683746.1:n.1706-10C>T (GMPPA)
ENST00000683752.1:c.405-10C>T (GMPPA) ENSP00000507197.1:n.405-10C>T
ENST00000683864.1:c.*1536-10C>T (GMPPA) ENSP00000507147.1:n.*1536-10C>T
ENST00000683946.1:c.756-10C>T (GMPPA) ENSP00000506941.1:n.756-10C>T
ENST00000684227.1:c.*787-10C>T (GMPPA) ENSP00000507190.1:n.*787-10C>T
ENST00000684242.1:n.1793+86C>T (GMPPA)
ENST00000684274.1:n.1126-10C>T (GMPPA)
ENST00000684334.1:n.1841-10C>T (GMPPA)
ENST00000684412.1:n.1102-10C>T (GMPPA)
ENST00000684562.1:n.1776-10C>T (GMPPA)
ENST00000684706.1:n.820-10C>T (GMPPA)
ENST00000684729.1:c.*787-10C>T (GMPPA) ENSP00000507441.1:n.*787-10C>T
ENST00000313597.10:c.756-10C>T (GMPPA) MANE Select ENSP00000315925.6:n.756-10C>T
ENST00000313597.9:c.756-10C>T (GMPPA) ENSP00000315925.5:n.756-10C>T
ENST00000341142.7:c.756-10C>T (GMPPA) ENSP00000340760.3:n.756-10C>T
ENST00000358215.8:c.756-10C>T (GMPPA) ENSP00000350949.3:n.756-10C>T
ENST00000373908.5:c.756-10C>T (GMPPA) ENSP00000363016.1:n.756-10C>T
ENST00000373917.7:c.756-10C>T (GMPPA) ENSP00000363027.3:n.756-10C>T
ENST00000435316.5:c.651-10C>T (GMPPA) ENSP00000411060.1:n.651-10C>T
ENST00000443704.5:c.756-10C>T (GMPPA) ENSP00000396750.1:n.756-10C>T
ENST00000481170.1:n.3584C>T (GMPPA)
ENST00000622191.1:c.756-10C>T (GMPPA) ENSP00000478700.1:n.756-10C>T
NM_013335.3:c.756-10C>T (GMPPA) NP_037467.2:n.756-10C>T
NM_205847.2:c.756-10C>T (GMPPA) NP_995319.1:n.756-10C>T
XM_005246483.2:c.771-10C>T (GMPPA) XP_005246540.1:n.771-10C>T
XM_005246485.2:c.771-10C>T (GMPPA) XP_005246542.1:n.771-10C>T
XM_005246486.2:c.756-10C>T (GMPPA) XP_005246543.1:n.756-10C>T
XM_011511032.1:c.771-10C>T (GMPPA) XP_011509334.1:n.771-10C>T
XM_011511033.1:c.396-10C>T (GMPPA) XP_011509335.1:n.396-10C>T
XM_011511034.1:c.771-10C>T (GMPPA) XP_011509336.1:n.771-10C>T
XM_011511035.1:c.770+86C>T (GMPPA) XP_011509337.1:n.770+86C>T
XR_241307.2:n.850-10C>T (GMPPA)
XR_923921.1:n.352+11248G>A (ASIC4-AS1)
XM_005246486.3:c.756-10C>T (GMPPA) XP_005246543.1:n.756-10C>T
XM_024452823.1:c.756-10C>T (GMPPA) XP_024308591.1:n.756-10C>T
XR_923921.2:n.391+11248G>A (ASIC4-AS1)
NM_001374294.1:c.756-10C>T (GMPPA) NP_001361223.1:n.756-10C>T
NM_001374295.1:c.756-10C>T (GMPPA) NP_001361224.1:n.756-10C>T
NM_013335.4:c.756-10C>T (GMPPA) MANE Select NP_037467.2:n.756-10C>T
NM_205847.3:c.756-10C>T (GMPPA) NP_995319.1:n.756-10C>T