Canonical Allele Identifier: CA409452570

Gene: GNAS

Linked Data

• MyVariant Identifiers: chr20:g.57484786G>T (hg19) ; chr20:g.58909731G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58909731G>T , CM000682.2:g.58909731G>T	GRCh38
NC_000020.10:g.57484786G>T , CM000682.1:g.57484786G>T	GRCh37
NC_000020.9:g.56918181G>T	NCBI36
NG_016194.1:g.74992G>T
NG_016194.2:g.74992G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349036.9:c.2650G>T	ENSP00000265621.6:p.Val884Phe
ENST00000419558.7:c.*624G>T	ENSP00000416234.2:n.*624G>T
ENST00000453292.7:c.1365G>T	ENSP00000392000.2:n.1365G>T
ENST00000462499.6:c.547G>T	ENSP00000499758.2:p.Val183Phe
ENST00000464624.7:c.*608G>T	ENSP00000499607.2:n.*608G>T
ENST00000464788.6:c.589G>T	ENSP00000499239.2:p.Val197Phe
ENST00000467227.6:c.547G>T	ENSP00000499681.2:p.Val183Phe
ENST00000467321.6:c.589G>T	ENSP00000499523.2:p.Val197Phe
ENST00000468895.6:c.766G>T	ENSP00000499551.2:p.Val256Phe
ENST00000469431.6:c.589G>T	ENSP00000499654.2:p.Val197Phe
ENST00000470512.6:c.592G>T	ENSP00000499552.2:p.Val198Phe
ENST00000472183.6:c.589G>T	ENSP00000499673.2:p.Val197Phe
ENST00000475610.2:n.1272G>T
ENST00000476935.6:c.544G>T	ENSP00000499409.2:p.Val182Phe
ENST00000478585.6:c.547G>T	ENSP00000499762.2:p.Val183Phe
ENST00000480232.6:c.592G>T	ENSP00000499545.2:p.Val198Phe
ENST00000481039.6:c.547G>T	ENSP00000499767.2:p.Val183Phe
ENST00000482112.6:c.544G>T	ENSP00000499794.2:p.Val182Phe
ENST00000485673.6:c.547G>T	ENSP00000499334.2:p.Val183Phe
ENST00000488546.6:c.547G>T	ENSP00000499332.2:p.Val183Phe
ENST00000488652.6:c.589G>T	ENSP00000499435.2:p.Val197Phe
ENST00000492907.6:c.547G>T	ENSP00000499443.2:p.Val183Phe
ENST00000603546.2:c.589G>T	ENSP00000474802.2:p.Val197Phe
ENST00000604005.6:c.589G>T	ENSP00000474219.2:p.Val197Phe
ENST00000663479.2:c.592G>T	ENSP00000499353.2:p.Val198Phe
ENST00000667293.2:c.589G>T	ENSP00000499293.2:p.Val197Phe
ENST00000676826.2:c.2698G>T	ENSP00000504675.2:p.Val900Phe
ENST00000682092.1:n.5050G>T
ENST00000682134.1:n.2692G>T
ENST00000682411.1:n.2861G>T
ENST00000682590.1:n.4953G>T
ENST00000682680.1:n.4967G>T
ENST00000682803.1:c.439G>T	ENSP00000507069.1:p.Val147Phe
ENST00000682829.1:n.3094G>T
ENST00000682917.1:n.1294G>T
ENST00000682986.1:n.5183G>T
ENST00000683015.1:c.1536G>T	ENSP00000506815.1:n.1536G>T
ENST00000683632.1:n.5296G>T
ENST00000683932.1:n.6542G>T
ENST00000684284.1:n.3144G>T
ENST00000684466.1:n.1405G>T
ENST00000684644.1:n.5086G>T
ENST00000684761.1:n.1259G>T
ENST00000306090.12:c.670G>T	ENSP00000304472.12:p.Val224Phe
ENST00000354359.12:c.769G>T	ENSP00000346328.7:p.Val257Phe
ENST00000371085.8:c.766G>T MANE Select	ENSP00000360126.3:p.Val256Phe
ENST00000371100.9:c.2695G>T MANE Plus Clinical	ENSP00000360141.3:p.Val899Phe
ENST00000656419.1:c.295G>T	ENSP00000499614.1:p.Val99Phe
ENST00000657090.1:c.589G>T	ENSP00000499380.1:p.Val197Phe
ENST00000667293.1:c.637G>T	ENSP00000499293.1:p.Val213Phe
ENST00000265620.11:c.721G>T	ENSP00000265620.7:p.Val241Phe
ENST00000306090.11:c.94-36G>T	ENSP00000304472.11:n.94-36G>T
ENST00000313949.11:c.*669G>T	ENSP00000323571.7:n.*669G>T
ENST00000354359.11:c.769G>T	ENSP00000346328.7:p.Val257Phe
ENST00000371075.7:c.*672G>T MANE Plus Clinical	ENSP00000360115.3:n.*672G>T
ENST00000371085.7:c.766G>T	ENSP00000360126.3:p.Val256Phe
ENST00000371095.7:c.724G>T	ENSP00000360136.3:p.Val242Phe
ENST00000371100.8:c.2695G>T	ENSP00000360141.3:p.Val899Phe
ENST00000371102.8:c.2653G>T	ENSP00000360143.4:p.Val885Phe
ENST00000464624.6:n.2982G>T
ENST00000470512.5:n.840G>T
ENST00000476196.5:n.1059G>T
ENST00000476935.5:n.755G>T
ENST00000477931.5:n.881G>T
ENST00000480232.5:n.785G>T
ENST00000480975.5:n.765G>T
ENST00000481039.5:n.683G>T
ENST00000487862.5:n.1000G>T
ENST00000488546.5:n.625G>T
ENST00000488652.5:n.856G>T
ENST00000492907.5:n.717G>T
ENST00000493958.5:n.489G>T
ENST00000494081.5:n.321G>T
ENST00000496934.5:n.2055G>T
NM_000516.4:c.766G>T	NP_000507.1:p.Val256Phe
NM_000516.5:c.766G>T	NP_000507.1:p.Val256Phe
NM_001077488.2:c.769G>T	NP_001070956.1:p.Val257Phe
NM_001077488.3:c.769G>T	NP_001070956.1:p.Val257Phe
NM_001077489.2:c.721G>T	NP_001070957.1:p.Val241Phe
NM_001077489.3:c.721G>T	NP_001070957.1:p.Val241Phe
NM_001077490.1:c.*627G>T	NP_001070958.1:n.*627G>T
NM_001077490.2:c.*627G>T	NP_001070958.1:n.*627G>T
NM_001309840.1:c.589G>T	NP_001296769.1:p.Val197Phe
NM_001309861.1:c.589G>T	NP_001296790.1:p.Val197Phe
NM_016592.2:c.*672G>T	NP_057676.1:n.*672G>T
NM_016592.3:c.*672G>T	NP_057676.1:n.*672G>T
NM_080425.2:c.2695G>T	NP_536350.2:p.Val899Phe
NM_080425.3:c.2695G>T	NP_536350.2:p.Val899Phe
NM_080426.2:c.724G>T	NP_536351.1:p.Val242Phe
NM_080426.3:c.724G>T	NP_536351.1:p.Val242Phe
NR_003259.1:c.-4294966440G>T
XM_017027812.2:c.2698G>T	XP_016883301.1:p.Val900Phe
XM_017027813.2:c.2653G>T	XP_016883302.1:p.Val885Phe
XM_017027814.2:c.2650G>T	XP_016883303.1:p.Val884Phe
XM_017027815.1:c.625G>T	XP_016883304.1:p.Val209Phe
XM_017027816.1:c.544G>T	XP_016883305.1:p.Val182Phe
XM_017027817.1:c.544G>T	XP_016883306.1:p.Val182Phe
XM_017027818.2:c.544G>T	XP_016883307.1:p.Val182Phe
XM_017027819.1:c.544G>T	XP_016883308.1:p.Val182Phe
XM_017027820.1:c.544G>T	XP_016883309.1:p.Val182Phe
XM_024451872.1:c.670G>T	XP_024307640.1:p.Val224Phe
XM_024451873.1:c.589G>T	XP_024307641.1:p.Val197Phe
XM_024451874.1:c.589G>T	XP_024307642.1:p.Val197Phe
XM_024451875.1:c.589G>T	XP_024307643.1:p.Val197Phe
XR_002958471.1:n.1473G>T
NM_000516.6:c.766G>T	NP_000507.1:p.Val256Phe
NM_001077488.4:c.769G>T	NP_001070956.1:p.Val257Phe
NM_001077489.4:c.721G>T	NP_001070957.1:p.Val241Phe
NM_001309840.2:c.589G>T	NP_001296769.1:p.Val197Phe
NM_001309861.2:c.589G>T	NP_001296790.1:p.Val197Phe
NM_016592.4:c.*672G>T	NP_057676.1:n.*672G>T
NM_080426.4:c.724G>T	NP_536351.1:p.Val242Phe
NM_000516.7:c.766G>T MANE Select	NP_000507.1:p.Val256Phe
NM_001077488.5:c.769G>T	NP_001070956.1:p.Val257Phe
NM_001077490.3:c.*627G>T	NP_001070958.1:n.*627G>T
NM_016592.5:c.*672G>T MANE Plus Clinical	NP_057676.1:n.*672G>T
NM_080425.4:c.2695G>T MANE Plus Clinical	NP_536350.2:p.Val899Phe