Canonical Allele Identifier: CA2577436733

Gene: GNAS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58909677G>T , CM000682.2:g.58909677G>T	GRCh38
NC_000020.10:g.57484732G>T , CM000682.1:g.57484732G>T	GRCh37
NC_000020.9:g.56918127G>T	NCBI36
NG_016194.1:g.74938G>T
NG_016194.2:g.74938G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349036.9:c.2603-7G>T	ENSP00000265621.6:n.2603-7G>T
ENST00000419558.7:c.*577-7G>T	ENSP00000416234.2:n.*577-7G>T
ENST00000453292.7:c.1318-7G>T	ENSP00000392000.2:n.1318-7G>T
ENST00000462499.6:c.500-7G>T	ENSP00000499758.2:n.500-7G>T
ENST00000464624.7:c.*561-7G>T	ENSP00000499607.2:n.*561-7G>T
ENST00000464788.6:c.542-7G>T	ENSP00000499239.2:n.542-7G>T
ENST00000467227.6:c.500-7G>T	ENSP00000499681.2:n.500-7G>T
ENST00000467321.6:c.542-7G>T	ENSP00000499523.2:n.542-7G>T
ENST00000468895.6:c.719-7G>T	ENSP00000499551.2:n.719-7G>T
ENST00000469431.6:c.542-7G>T	ENSP00000499654.2:n.542-7G>T
ENST00000470512.6:c.545-7G>T	ENSP00000499552.2:n.545-7G>T
ENST00000472183.6:c.542-7G>T	ENSP00000499673.2:n.542-7G>T
ENST00000475610.2:n.1225-7G>T
ENST00000476935.6:c.497-7G>T	ENSP00000499409.2:n.497-7G>T
ENST00000478585.6:c.500-7G>T	ENSP00000499762.2:n.500-7G>T
ENST00000480232.6:c.545-7G>T	ENSP00000499545.2:n.545-7G>T
ENST00000481039.6:c.500-7G>T	ENSP00000499767.2:n.500-7G>T
ENST00000482112.6:c.497-7G>T	ENSP00000499794.2:n.497-7G>T
ENST00000485673.6:c.500-7G>T	ENSP00000499334.2:n.500-7G>T
ENST00000488546.6:c.500-7G>T	ENSP00000499332.2:n.500-7G>T
ENST00000488652.6:c.542-7G>T	ENSP00000499435.2:n.542-7G>T
ENST00000492907.6:c.500-7G>T	ENSP00000499443.2:n.500-7G>T
ENST00000603546.2:c.542-7G>T	ENSP00000474802.2:n.542-7G>T
ENST00000604005.6:c.542-7G>T	ENSP00000474219.2:n.542-7G>T
ENST00000663479.2:c.545-7G>T	ENSP00000499353.2:n.545-7G>T
ENST00000667293.2:c.542-7G>T	ENSP00000499293.2:n.542-7G>T
ENST00000676826.2:c.2651-7G>T	ENSP00000504675.2:n.2651-7G>T
ENST00000682092.1:n.5003-7G>T
ENST00000682134.1:n.2645-7G>T
ENST00000682411.1:n.2814-7G>T
ENST00000682590.1:n.4906-7G>T
ENST00000682680.1:n.4920-7G>T
ENST00000682803.1:c.392-7G>T	ENSP00000507069.1:n.392-7G>T
ENST00000682829.1:n.3047-7G>T
ENST00000682917.1:n.1247-7G>T
ENST00000682986.1:n.5136-7G>T
ENST00000683015.1:c.1489-7G>T	ENSP00000506815.1:n.1489-7G>T
ENST00000683632.1:n.5242G>T
ENST00000683932.1:n.6495-7G>T
ENST00000684284.1:n.3097-7G>T
ENST00000684466.1:n.1358-7G>T
ENST00000684644.1:n.5039-7G>T
ENST00000684761.1:n.1212-7G>T
ENST00000306090.12:c.623-7G>T	ENSP00000304472.12:n.623-7G>T
ENST00000354359.12:c.722-7G>T	ENSP00000346328.7:n.722-7G>T
ENST00000371085.8:c.719-7G>T MANE Select	ENSP00000360126.3:n.719-7G>T
ENST00000371100.9:c.2648-7G>T MANE Plus Clinical	ENSP00000360141.3:n.2648-7G>T
ENST00000656419.1:c.248-7G>T	ENSP00000499614.1:n.248-7G>T
ENST00000657090.1:c.542-7G>T	ENSP00000499380.1:n.542-7G>T
ENST00000667293.1:c.590-7G>T	ENSP00000499293.1:n.590-7G>T
ENST00000265620.11:c.674-7G>T	ENSP00000265620.7:n.674-7G>T
ENST00000306090.11:c.94-90G>T	ENSP00000304472.11:n.94-90G>T
ENST00000313949.11:c.*622-7G>T	ENSP00000323571.7:n.*622-7G>T
ENST00000354359.11:c.722-7G>T	ENSP00000346328.7:n.722-7G>T
ENST00000371075.7:c.*625-7G>T MANE Plus Clinical	ENSP00000360115.3:n.*625-7G>T
ENST00000371085.7:c.719-7G>T	ENSP00000360126.3:n.719-7G>T
ENST00000371095.7:c.677-7G>T	ENSP00000360136.3:n.677-7G>T
ENST00000371100.8:c.2648-7G>T	ENSP00000360141.3:n.2648-7G>T
ENST00000371102.8:c.2606-7G>T	ENSP00000360143.4:n.2606-7G>T
ENST00000464624.6:n.2935-7G>T
ENST00000470512.5:n.793-7G>T
ENST00000476196.5:n.1012-7G>T
ENST00000476935.5:n.708-7G>T
ENST00000477931.5:n.834-7G>T
ENST00000479025.1:n.435-7G>T
ENST00000480232.5:n.738-7G>T
ENST00000480975.5:n.718-7G>T
ENST00000481039.5:n.636-7G>T
ENST00000487862.5:n.953-7G>T
ENST00000487981.5:n.553-7G>T
ENST00000488546.5:n.578-7G>T
ENST00000488652.5:n.809-7G>T
ENST00000492907.5:n.670-7G>T
ENST00000493958.5:n.435G>T
ENST00000494081.5:n.274-7G>T
ENST00000496934.5:n.2008-7G>T
NM_000516.4:c.719-7G>T	NP_000507.1:n.719-7G>T
NM_000516.5:c.719-7G>T	NP_000507.1:n.719-7G>T
NM_001077488.2:c.722-7G>T	NP_001070956.1:n.722-7G>T
NM_001077488.3:c.722-7G>T	NP_001070956.1:n.722-7G>T
NM_001077489.2:c.674-7G>T	NP_001070957.1:n.674-7G>T
NM_001077489.3:c.674-7G>T	NP_001070957.1:n.674-7G>T
NM_001077490.1:c.*580-7G>T	NP_001070958.1:n.*580-7G>T
NM_001077490.2:c.*580-7G>T	NP_001070958.1:n.*580-7G>T
NM_001309840.1:c.542-7G>T	NP_001296769.1:n.542-7G>T
NM_001309861.1:c.542-7G>T	NP_001296790.1:n.542-7G>T
NM_016592.2:c.*625-7G>T	NP_057676.1:n.*625-7G>T
NM_016592.3:c.*625-7G>T	NP_057676.1:n.*625-7G>T
NM_080425.2:c.2648-7G>T	NP_536350.2:n.2648-7G>T
NM_080425.3:c.2648-7G>T	NP_536350.2:n.2648-7G>T
NM_080426.2:c.677-7G>T	NP_536351.1:n.677-7G>T
NM_080426.3:c.677-7G>T	NP_536351.1:n.677-7G>T
NR_003259.1:c.-4294966487-7G>T
XM_017027812.2:c.2651-7G>T	XP_016883301.1:n.2651-7G>T
XM_017027813.2:c.2606-7G>T	XP_016883302.1:n.2606-7G>T
XM_017027814.2:c.2603-7G>T	XP_016883303.1:n.2603-7G>T
XM_017027815.1:c.578-7G>T	XP_016883304.1:n.578-7G>T
XM_017027816.1:c.497-7G>T	XP_016883305.1:n.497-7G>T
XM_017027817.1:c.497-7G>T	XP_016883306.1:n.497-7G>T
XM_017027818.2:c.497-7G>T	XP_016883307.1:n.497-7G>T
XM_017027819.1:c.497-7G>T	XP_016883308.1:n.497-7G>T
XM_017027820.1:c.497-7G>T	XP_016883309.1:n.497-7G>T
XM_024451872.1:c.623-7G>T	XP_024307640.1:n.623-7G>T
XM_024451873.1:c.542-7G>T	XP_024307641.1:n.542-7G>T
XM_024451874.1:c.542-7G>T	XP_024307642.1:n.542-7G>T
XM_024451875.1:c.542-7G>T	XP_024307643.1:n.542-7G>T
XR_002958471.1:n.1426-7G>T
NM_000516.6:c.719-7G>T	NP_000507.1:n.719-7G>T
NM_001077488.4:c.722-7G>T	NP_001070956.1:n.722-7G>T
NM_001077489.4:c.674-7G>T	NP_001070957.1:n.674-7G>T
NM_001309840.2:c.542-7G>T	NP_001296769.1:n.542-7G>T
NM_001309861.2:c.542-7G>T	NP_001296790.1:n.542-7G>T
NM_016592.4:c.*625-7G>T	NP_057676.1:n.*625-7G>T
NM_080426.4:c.677-7G>T	NP_536351.1:n.677-7G>T
NM_000516.7:c.719-7G>T MANE Select	NP_000507.1:n.719-7G>T
NM_001077488.5:c.722-7G>T	NP_001070956.1:n.722-7G>T
NM_001077490.3:c.*580-7G>T	NP_001070958.1:n.*580-7G>T
NM_016592.5:c.*625-7G>T MANE Plus Clinical	NP_057676.1:n.*625-7G>T
NM_080425.4:c.2648-7G>T MANE Plus Clinical	NP_536350.2:n.2648-7G>T