Canonical Allele Identifier: CA2372529378
Gene: GNAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.58909749C= , CM000682.2:g.58909749C= GRCh38
NC_000020.10:g.57484804C= , CM000682.1:g.57484804C= GRCh37
NC_000020.9:g.56918199C= NCBI36
NG_016194.1:g.75010C=
NG_016194.2:g.75010C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000349036.9:c.2668C= ENSP00000265621.6:p.Gln890=
ENST00000419558.7:c.*642C= ENSP00000416234.2:n.*642C=
ENST00000453292.7:c.1383C= ENSP00000392000.2:n.1383C=
ENST00000462499.6:c.565C= ENSP00000499758.2:p.Gln189=
ENST00000464624.7:c.*626C= ENSP00000499607.2:n.*626C=
ENST00000464788.6:c.607C= ENSP00000499239.2:p.Gln203=
ENST00000467227.6:c.565C= ENSP00000499681.2:p.Gln189=
ENST00000467321.6:c.607C= ENSP00000499523.2:p.Gln203=
ENST00000468895.6:c.784C= ENSP00000499551.2:p.Gln262=
ENST00000469431.6:c.607C= ENSP00000499654.2:p.Gln203=
ENST00000470512.6:c.610C= ENSP00000499552.2:p.Gln204=
ENST00000472183.6:c.607C= ENSP00000499673.2:p.Gln203=
ENST00000475610.2:n.1290C=
ENST00000476935.6:c.562C= ENSP00000499409.2:p.Gln188=
ENST00000478585.6:c.565C= ENSP00000499762.2:p.Gln189=
ENST00000480232.6:c.610C= ENSP00000499545.2:p.Gln204=
ENST00000481039.6:c.565C= ENSP00000499767.2:p.Gln189=
ENST00000482112.6:c.562C= ENSP00000499794.2:p.Gln188=
ENST00000485673.6:c.565C= ENSP00000499334.2:p.Gln189=
ENST00000488546.6:c.565C= ENSP00000499332.2:p.Gln189=
ENST00000488652.6:c.607C= ENSP00000499435.2:p.Gln203=
ENST00000492907.6:c.565C= ENSP00000499443.2:p.Gln189=
ENST00000603546.2:c.607C= ENSP00000474802.2:p.Gln203=
ENST00000604005.6:c.607C= ENSP00000474219.2:p.Gln203=
ENST00000663479.2:c.610C= ENSP00000499353.2:p.Gln204=
ENST00000667293.2:c.607C= ENSP00000499293.2:p.Gln203=
ENST00000676826.2:c.2716C= ENSP00000504675.2:p.Gln906=
ENST00000682092.1:n.5068C=
ENST00000682134.1:n.2710C=
ENST00000682411.1:n.2879C=
ENST00000682590.1:n.4971C=
ENST00000682680.1:n.4985C=
ENST00000682803.1:c.457C= ENSP00000507069.1:p.Gln153=
ENST00000682829.1:n.3112C=
ENST00000682917.1:n.1312C=
ENST00000682986.1:n.5201C=
ENST00000683015.1:c.1554C= ENSP00000506815.1:n.1554C=
ENST00000683632.1:n.5314C=
ENST00000683932.1:n.6560C=
ENST00000684284.1:n.3162C=
ENST00000684466.1:n.1423C=
ENST00000684644.1:n.5104C=
ENST00000684761.1:n.1277C=
ENST00000306090.12:c.688C= ENSP00000304472.12:p.Gln230=
ENST00000354359.12:c.787C= ENSP00000346328.7:p.Gln263=
ENST00000371085.8:c.784C= MANE Select ENSP00000360126.3:p.Gln262=
ENST00000371100.9:c.2713C= MANE Plus Clinical ENSP00000360141.3:p.Gln905=
ENST00000656419.1:c.313C= ENSP00000499614.1:p.Gln105=
ENST00000657090.1:c.607C= ENSP00000499380.1:p.Gln203=
ENST00000667293.1:c.655C= ENSP00000499293.1:p.Gln219=
ENST00000265620.11:c.739C= ENSP00000265620.7:p.Gln247=
ENST00000306090.11:c.94-18C= ENSP00000304472.11:n.94-18C=
ENST00000313949.11:c.*687C= ENSP00000323571.7:n.*687C=
ENST00000354359.11:c.787C= ENSP00000346328.7:p.Gln263=
ENST00000371075.7:c.*690C= MANE Plus Clinical ENSP00000360115.3:n.*690C=
ENST00000371085.7:c.784C= ENSP00000360126.3:p.Gln262=
ENST00000371095.7:c.742C= ENSP00000360136.3:p.Gln248=
ENST00000371100.8:c.2713C= ENSP00000360141.3:p.Gln905=
ENST00000371102.8:c.2671C= ENSP00000360143.4:p.Gln891=
ENST00000464624.6:n.3000C=
ENST00000470512.5:n.858C=
ENST00000476196.5:n.1077C=
ENST00000476935.5:n.773C=
ENST00000477931.5:n.899C=
ENST00000480232.5:n.803C=
ENST00000480975.5:n.783C=
ENST00000481039.5:n.701C=
ENST00000487862.5:n.1018C=
ENST00000488546.5:n.643C=
ENST00000488652.5:n.874C=
ENST00000492907.5:n.735C=
ENST00000493958.5:n.507C=
ENST00000494081.5:n.339C=
ENST00000496934.5:n.2073C=
NM_000516.4:c.784C= NP_000507.1:p.Gln262=
NM_000516.5:c.784C= NP_000507.1:p.Gln262=
NM_001077488.2:c.787C= NP_001070956.1:p.Gln263=
NM_001077488.3:c.787C= NP_001070956.1:p.Gln263=
NM_001077489.2:c.739C= NP_001070957.1:p.Gln247=
NM_001077489.3:c.739C= NP_001070957.1:p.Gln247=
NM_001077490.1:c.*645C= NP_001070958.1:n.*645C=
NM_001077490.2:c.*645C= NP_001070958.1:n.*645C=
NM_001309840.1:c.607C= NP_001296769.1:p.Gln203=
NM_001309861.1:c.607C= NP_001296790.1:p.Gln203=
NM_016592.2:c.*690C= NP_057676.1:n.*690C=
NM_016592.3:c.*690C= NP_057676.1:n.*690C=
NM_080425.2:c.2713C= NP_536350.2:p.Gln905=
NM_080425.3:c.2713C= NP_536350.2:p.Gln905=
NM_080426.2:c.742C= NP_536351.1:p.Gln248=
NM_080426.3:c.742C= NP_536351.1:p.Gln248=
NR_003259.1:c.-4294966422C=
XM_017027812.2:c.2716C= XP_016883301.1:p.Gln906=
XM_017027813.2:c.2671C= XP_016883302.1:p.Gln891=
XM_017027814.2:c.2668C= XP_016883303.1:p.Gln890=
XM_017027815.1:c.643C= XP_016883304.1:p.Gln215=
XM_017027816.1:c.562C= XP_016883305.1:p.Gln188=
XM_017027817.1:c.562C= XP_016883306.1:p.Gln188=
XM_017027818.2:c.562C= XP_016883307.1:p.Gln188=
XM_017027819.1:c.562C= XP_016883308.1:p.Gln188=
XM_017027820.1:c.562C= XP_016883309.1:p.Gln188=
XM_024451872.1:c.688C= XP_024307640.1:p.Gln230=
XM_024451873.1:c.607C= XP_024307641.1:p.Gln203=
XM_024451874.1:c.607C= XP_024307642.1:p.Gln203=
XM_024451875.1:c.607C= XP_024307643.1:p.Gln203=
XR_002958471.1:n.1491C=
NM_000516.6:c.784C= NP_000507.1:p.Gln262=
NM_001077488.4:c.787C= NP_001070956.1:p.Gln263=
NM_001077489.4:c.739C= NP_001070957.1:p.Gln247=
NM_001309840.2:c.607C= NP_001296769.1:p.Gln203=
NM_001309861.2:c.607C= NP_001296790.1:p.Gln203=
NM_016592.4:c.*690C= NP_057676.1:n.*690C=
NM_080426.4:c.742C= NP_536351.1:p.Gln248=
NM_000516.7:c.784C= MANE Select NP_000507.1:p.Gln262=
NM_001077488.5:c.787C= NP_001070956.1:p.Gln263=
NM_001077490.3:c.*645C= NP_001070958.1:n.*645C=
NM_016592.5:c.*690C= MANE Plus Clinical NP_057676.1:n.*690C=
NM_080425.4:c.2713C= MANE Plus Clinical NP_536350.2:p.Gln905=