Canonical Allele Identifier: CA2695229882
Gene: GNAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.58891727_58891736del , CM000682.2:g.58891727_58891736del GRCh38
NC_000020.10:g.57466782_57466791del , CM000682.1:g.57466782_57466791del GRCh37
NC_000020.9:g.56900177_56900186del NCBI36
NG_016194.1:g.56988_56997del
NG_016194.2:g.56988_56997del

Transcript Alleles

HGVS Amino-acid change
ENST00000349036.9:c.2069-3885_2069-3876del ENSP00000265621.6:n.2069-3885_2069-3876de...
ENST00000419558.7:c.*43-3885_*43-3876del ENSP00000416234.2:n.*43-3885_*43-3876del
ENST00000423897.7:c.2069-3885_2069-3876del ENSP00000412356.2:n.2069-3885_2069-3876de...
ENST00000453292.7:c.781-3885_781-3876del ENSP00000392000.2:n.781-3885_781-3876del
ENST00000462499.6:c.-38-3885_-38-3876del ENSP00000499758.2:n.-38-3885_-38-3876del
ENST00000464624.7:c.2160-3885_2160-3876del ENSP00000499607.2:n.2160-3885_2160-3876de...
ENST00000464788.6:c.-39+2514_-39+2523del ENSP00000499239.2:n.-39+2514_-39+2523del
ENST00000467227.6:c.-38-3885_-38-3876del ENSP00000499681.2:n.-38-3885_-38-3876del
ENST00000467321.6:c.-39+2681_-39+2690del ENSP00000499523.2:n.-39+2681_-39+2690del
ENST00000468895.6:c.1_10del ENSP00000499551.2:p.Met1SerfsTer?
ENST00000469431.6:c.-39+2321_-39+2330del ENSP00000499654.2:n.-39+2321_-39+2330del
ENST00000470512.6:c.-39+2374_-39+2383del ENSP00000499552.2:n.-39+2374_-39+2383del
ENST00000472183.6:c.-38-3885_-38-3876del ENSP00000499673.2:n.-38-3885_-38-3876del
ENST00000478585.6:c.-39+2374_-39+2383del ENSP00000499762.2:n.-39+2374_-39+2383del
ENST00000480232.6:c.-39+2178_-39+2187del ENSP00000499545.2:n.-39+2178_-39+2187del
ENST00000481039.6:c.-39+2819_-39+2828del ENSP00000499767.2:n.-39+2819_-39+2828del
ENST00000482112.6:c.-38-3885_-38-3876del ENSP00000499794.2:n.-38-3885_-38-3876del
ENST00000485673.6:c.-39+2178_-39+2187del ENSP00000499334.2:n.-39+2178_-39+2187del
ENST00000488546.6:c.-39+2909_-39+2918del ENSP00000499332.2:n.-39+2909_-39+2918del
ENST00000604005.6:c.-39+2395_-39+2404del ENSP00000474219.2:n.-39+2395_-39+2404del
ENST00000663479.2:c.-38-3885_-38-3876del ENSP00000499353.2:n.-38-3885_-38-3876del
ENST00000667293.2:c.-39+2823_-39+2832del ENSP00000499293.2:n.-39+2823_-39+2832del
ENST00000676826.2:c.2069-3885_2069-3876del ENSP00000504675.2:n.2069-3885_2069-3876de...
ENST00000683015.1:c.909+938_909+947del ENSP00000506815.1:n.909+938_909+947del
ENST00000306090.12:c.44-3885_44-3876del ENSP00000304472.12:n.44-3885_44-3876del
ENST00000349036.8:c.2069-3885_2069-3876del ENSP00000265621.5:n.2069-3885_2069-3876de...
ENST00000354359.12:c.1_10del ENSP00000346328.7:p.Met1SerfsTer?
ENST00000371085.8:c.1_10del MANE Select ENSP00000360126.3:p.Met1SerfsTer?
ENST00000371100.9:c.2069-3885_2069-3876del MANE Plus Clinical ENSP00000360141.3:n.2069-3885_2069-3876de...
ENST00000419558.6:c.*43-3885_*43-3876del ENSP00000416234.2:n.*43-3885_*43-3876del
ENST00000423897.6:c.2069-3885_2069-3876del ENSP00000412356.2:n.2069-3885_2069-3876de...
ENST00000453292.6:c.*43-3885_*43-3876del ENSP00000392000.2:n.*43-3885_*43-3876del
ENST00000461152.6:c.909+938_909+947del ENSP00000499274.1:n.909+938_909+947del
ENST00000481768.6:c.2227-3885_2227-3876del ENSP00000499644.2:n.2227-3885_2227-3876de...
ENST00000490374.6:n.223-3885_223-3876del
ENST00000657090.1:c.-38-3885_-38-3876del ENSP00000499380.1:n.-38-3885_-38-3876del
ENST00000663479.1:c.-38-3885_-38-3876del ENSP00000499353.1:n.-38-3885_-38-3876del
ENST00000667293.1:c.11-3885_11-3876del ENSP00000499293.1:n.11-3885_11-3876del
ENST00000676826.1:c.2069-3885_2069-3876del ENSP00000504675.1:n.2069-3885_2069-3876de...
ENST00000265620.11:c.1_10del ENSP00000265620.7:p.Met1SerfsTer?
ENST00000313949.11:c.*43-3885_*43-3876del ENSP00000323571.7:n.*43-3885_*43-3876del
ENST00000349036.7:c.188-3885_188-3876del ENSP00000265621.4:n.188-3885_188-3876del
ENST00000354359.11:c.1_10del ENSP00000346328.7:p.Met1SerfsTer?
ENST00000371075.7:c.*43-3885_*43-3876del MANE Plus Clinical ENSP00000360115.3:n.*43-3885_*43-3876del
ENST00000371081.5:c.1_10del ENSP00000360122.1:p.Met1SerfsTer?
ENST00000371085.7:c.1_10del ENSP00000360126.3:p.Met1SerfsTer?
ENST00000371095.7:c.1_10del ENSP00000360136.3:p.Met1SerfsTer?
ENST00000371098.6:c.*43-3885_*43-3876del ENSP00000360139.2:n.*43-3885_*43-3876del
ENST00000371100.8:c.2069-3885_2069-3876del ENSP00000360141.3:n.2069-3885_2069-3876de...
ENST00000371102.8:c.2069-3885_2069-3876del ENSP00000360143.4:n.2069-3885_2069-3876de...
ENST00000419558.5:c.384-3885_384-3876del
ENST00000423897.5:c.157-3885_157-3876del
ENST00000450130.5:c.228-3885_228-3876del
ENST00000453292.5:c.544-3885_544-3876del ENSP00000392000.1:n.544-3885_544-3876del
ENST00000461152.5:n.147+938_147+947del
ENST00000462499.5:n.259-3885_259-3876del
ENST00000464624.6:n.2217_2226del
ENST00000464788.5:n.67+2514_67+2523del
ENST00000464960.5:n.406+2909_406+2918del
ENST00000467227.5:n.123-3885_123-3876del
ENST00000467321.5:n.154+2681_154+2690del
ENST00000468895.5:n.50+2819_50+2828del
ENST00000469431.5:n.256+2321_256+2330del
ENST00000470512.5:n.210+2374_210+2383del
ENST00000472183.5:n.392-3885_392-3876del
ENST00000477931.5:n.254+2374_254+2383del
ENST00000478585.5:n.194+2374_194+2383del
ENST00000480232.5:n.155+2178_155+2187del
ENST00000480975.5:n.183+2374_183+2383del
ENST00000481039.5:n.56+2823_56+2832del
ENST00000481768.5:n.1324-3885_1324-3876del
ENST00000482112.5:n.259-3885_259-3876del
ENST00000484504.5:n.127+2374_127+2383del
ENST00000485673.5:n.426+2178_426+2187del
ENST00000488546.5:n.40+2909_40+2918del
ENST00000490374.5:n.255-3885_255-3876del
ENST00000491348.5:n.534-3885_534-3876del
ENST00000493744.5:n.233-3885_233-3876del
ENST00000604005.5:c.-39+2395_-39+2404del ENSP00000474219.1:n.-39+2395_-39+2404del
NM_000516.4:c.1_10del NP_000507.1:p.Met1SerfsTer?
NM_000516.5:c.1_10del NP_000507.1:p.Met1SerfsTer?
NM_001077488.2:c.1_10del NP_001070956.1:p.Met1SerfsTer?
NM_001077488.3:c.1_10del NP_001070956.1:p.Met1SerfsTer?
NM_001077489.2:c.1_10del NP_001070957.1:p.Met1SerfsTer?
NM_001077489.3:c.1_10del NP_001070957.1:p.Met1SerfsTer?
NM_001077490.1:c.*1-3885_*1-3876del NP_001070958.1:n.*1-3885_*1-3876del
NM_001077490.2:c.*1-3885_*1-3876del NP_001070958.1:n.*1-3885_*1-3876del
NM_001309840.1:c.-39+2374_-39+2383del NP_001296769.1:n.-39+2374_-39+2383del
NM_001309842.1:c.1_10del NP_001296771.1:p.Met1SerfsTer?
NM_001309861.1:c.-38-3885_-38-3876del NP_001296790.1:n.-38-3885_-38-3876del
NM_001309883.1:c.*159-3885_*159-3876del NP_001296812.1:n.*159-3885_*159-3876del
NM_016592.2:c.*43-3885_*43-3876del NP_057676.1:n.*43-3885_*43-3876del
NM_016592.3:c.*43-3885_*43-3876del NP_057676.1:n.*43-3885_*43-3876del
NM_080425.2:c.2069-3885_2069-3876del NP_536350.2:n.2069-3885_2069-3876del
NM_080425.3:c.2069-3885_2069-3876del NP_536350.2:n.2069-3885_2069-3876del
NM_080426.2:c.1_10del NP_536351.1:p.Met1SerfsTer?
NM_080426.3:c.1_10del NP_536351.1:p.Met1SerfsTer?
NR_003259.1:c.-4294967067+2374_-4294967067+2383del
NR_132273.1:n.406+2909_406+2918del
XM_017027812.2:c.2069-3885_2069-3876del XP_016883301.1:n.2069-3885_2069-3876del
XM_017027813.2:c.2069-3885_2069-3876del XP_016883302.1:n.2069-3885_2069-3876del
XM_017027814.2:c.2069-3885_2069-3876del XP_016883303.1:n.2069-3885_2069-3876del
XM_017027815.1:c.44-3885_44-3876del XP_016883304.1:n.44-3885_44-3876del
XM_017027816.1:c.-304_-295del XP_016883305.1:n.-304_-295del
XM_017027817.1:c.-39+2374_-39+2383del XP_016883306.1:n.-39+2374_-39+2383del
XM_017027819.1:c.-39+2395_-39+2404del XP_016883308.1:n.-39+2395_-39+2404del
XM_017027821.1:c.*43-3885_*43-3876del XP_016883310.1:n.*43-3885_*43-3876del
XM_017027822.1:c.*43-3885_*43-3876del XP_016883311.1:n.*43-3885_*43-3876del
XM_024451872.1:c.44-3885_44-3876del XP_024307640.1:n.44-3885_44-3876del
XM_024451875.1:c.-39+2395_-39+2404del XP_024307643.1:n.-39+2395_-39+2404del
XR_002958471.1:n.626_635del
NM_000516.6:c.1_10del NP_000507.1:p.Met1SerfsTer?
NM_001077488.4:c.1_10del NP_001070956.1:p.Met1SerfsTer?
NM_001077489.4:c.1_10del NP_001070957.1:p.Met1SerfsTer?
NM_001309840.2:c.-39+2374_-39+2383del NP_001296769.1:n.-39+2374_-39+2383del
NM_001309842.2:c.1_10del NP_001296771.1:p.Met1SerfsTer?
NM_001309861.2:c.-38-3885_-38-3876del NP_001296790.1:n.-38-3885_-38-3876del
NM_016592.4:c.*43-3885_*43-3876del NP_057676.1:n.*43-3885_*43-3876del
NM_080426.4:c.1_10del NP_536351.1:p.Met1SerfsTer?
NM_000516.7:c.1_10del MANE Select NP_000507.1:p.Met1SerfsTer?
NM_001077488.5:c.1_10del NP_001070956.1:p.Met1SerfsTer?
NM_001077490.3:c.*1-3885_*1-3876del NP_001070958.1:n.*1-3885_*1-3876del
NM_016592.5:c.*43-3885_*43-3876del MANE Plus Clinical NP_057676.1:n.*43-3885_*43-3876del
NM_080425.4:c.2069-3885_2069-3876del MANE Plus Clinical NP_536350.2:n.2069-3885_2069-3876del