Canonical Allele Identifier: CA511087399

Gene: GNAS

Linked Data

• MyVariant Identifiers: chr20:g.57484815C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58909760C>G , CM000682.2:g.58909760C>G	GRCh38
NC_000020.10:g.57484815C>G , CM000682.1:g.57484815C>G	GRCh37
NC_000020.9:g.56918210C>G	NCBI36
NG_016194.1:g.75021C>G
NG_016194.2:g.75021C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349036.9:c.2679C>G	ENSP00000265621.6:p.Arg893=
ENST00000419558.7:c.*653C>G	ENSP00000416234.2:n.*653C>G
ENST00000453292.7:c.1394C>G	ENSP00000392000.2:n.1394C>G
ENST00000462499.6:c.576C>G	ENSP00000499758.2:p.Arg192=
ENST00000464624.7:c.*637C>G	ENSP00000499607.2:n.*637C>G
ENST00000464788.6:c.618C>G	ENSP00000499239.2:p.Arg206=
ENST00000467227.6:c.576C>G	ENSP00000499681.2:p.Arg192=
ENST00000467321.6:c.618C>G	ENSP00000499523.2:p.Arg206=
ENST00000468895.6:c.795C>G	ENSP00000499551.2:p.Arg265=
ENST00000469431.6:c.618C>G	ENSP00000499654.2:p.Arg206=
ENST00000470512.6:c.621C>G	ENSP00000499552.2:p.Arg207=
ENST00000472183.6:c.618C>G	ENSP00000499673.2:p.Arg206=
ENST00000475610.2:n.1301C>G
ENST00000476935.6:c.573C>G	ENSP00000499409.2:p.Arg191=
ENST00000478585.6:c.576C>G	ENSP00000499762.2:p.Arg192=
ENST00000480232.6:c.621C>G	ENSP00000499545.2:p.Arg207=
ENST00000481039.6:c.576C>G	ENSP00000499767.2:p.Arg192=
ENST00000482112.6:c.573C>G	ENSP00000499794.2:p.Arg191=
ENST00000485673.6:c.576C>G	ENSP00000499334.2:p.Arg192=
ENST00000488546.6:c.576C>G	ENSP00000499332.2:p.Arg192=
ENST00000488652.6:c.618C>G	ENSP00000499435.2:p.Arg206=
ENST00000492907.6:c.576C>G	ENSP00000499443.2:p.Arg192=
ENST00000603546.2:c.618C>G	ENSP00000474802.2:p.Arg206=
ENST00000604005.6:c.618C>G	ENSP00000474219.2:p.Arg206=
ENST00000663479.2:c.621C>G	ENSP00000499353.2:p.Arg207=
ENST00000667293.2:c.618C>G	ENSP00000499293.2:p.Arg206=
ENST00000676826.2:c.2727C>G	ENSP00000504675.2:p.Arg909=
ENST00000682092.1:n.5079C>G
ENST00000682134.1:n.2721C>G
ENST00000682411.1:n.2890C>G
ENST00000682590.1:n.4982C>G
ENST00000682680.1:n.4996C>G
ENST00000682803.1:c.468C>G	ENSP00000507069.1:p.Arg156=
ENST00000682829.1:n.3123C>G
ENST00000682917.1:n.1323C>G
ENST00000682986.1:n.5212C>G
ENST00000683015.1:c.1565C>G	ENSP00000506815.1:n.1565C>G
ENST00000683632.1:n.5325C>G
ENST00000683932.1:n.6571C>G
ENST00000684284.1:n.3173C>G
ENST00000684466.1:n.1434C>G
ENST00000684644.1:n.5115C>G
ENST00000684761.1:n.1288C>G
ENST00000306090.12:c.699C>G	ENSP00000304472.12:p.Arg233=
ENST00000354359.12:c.798C>G	ENSP00000346328.7:p.Arg266=
ENST00000371085.8:c.795C>G MANE Select	ENSP00000360126.3:p.Arg265=
ENST00000371100.9:c.2724C>G MANE Plus Clinical	ENSP00000360141.3:p.Arg908=
ENST00000656419.1:c.324C>G	ENSP00000499614.1:p.Arg108=
ENST00000657090.1:c.618C>G	ENSP00000499380.1:p.Arg206=
ENST00000667293.1:c.666C>G	ENSP00000499293.1:p.Arg222=
ENST00000265620.11:c.750C>G	ENSP00000265620.7:p.Arg250=
ENST00000306090.11:c.94-7C>G	ENSP00000304472.11:n.94-7C>G
ENST00000313949.11:c.*698C>G	ENSP00000323571.7:n.*698C>G
ENST00000354359.11:c.798C>G	ENSP00000346328.7:p.Arg266=
ENST00000371075.7:c.*701C>G MANE Plus Clinical	ENSP00000360115.3:n.*701C>G
ENST00000371085.7:c.795C>G	ENSP00000360126.3:p.Arg265=
ENST00000371095.7:c.753C>G	ENSP00000360136.3:p.Arg251=
ENST00000371100.8:c.2724C>G	ENSP00000360141.3:p.Arg908=
ENST00000371102.8:c.2682C>G	ENSP00000360143.4:p.Arg894=
ENST00000464624.6:n.3011C>G
ENST00000470512.5:n.869C>G
ENST00000476196.5:n.1088C>G
ENST00000476935.5:n.784C>G
ENST00000477931.5:n.910C>G
ENST00000480232.5:n.814C>G
ENST00000480975.5:n.794C>G
ENST00000481039.5:n.712C>G
ENST00000487862.5:n.1029C>G
ENST00000488546.5:n.654C>G
ENST00000488652.5:n.885C>G
ENST00000492907.5:n.746C>G
ENST00000493958.5:n.518C>G
ENST00000494081.5:n.350C>G
ENST00000496934.5:n.2084C>G
NM_000516.4:c.795C>G	NP_000507.1:p.Arg265=
NM_000516.5:c.795C>G	NP_000507.1:p.Arg265=
NM_001077488.2:c.798C>G	NP_001070956.1:p.Arg266=
NM_001077488.3:c.798C>G	NP_001070956.1:p.Arg266=
NM_001077489.2:c.750C>G	NP_001070957.1:p.Arg250=
NM_001077489.3:c.750C>G	NP_001070957.1:p.Arg250=
NM_001077490.1:c.*656C>G	NP_001070958.1:n.*656C>G
NM_001077490.2:c.*656C>G	NP_001070958.1:n.*656C>G
NM_001309840.1:c.618C>G	NP_001296769.1:p.Arg206=
NM_001309861.1:c.618C>G	NP_001296790.1:p.Arg206=
NM_016592.2:c.*701C>G	NP_057676.1:n.*701C>G
NM_016592.3:c.*701C>G	NP_057676.1:n.*701C>G
NM_080425.2:c.2724C>G	NP_536350.2:p.Arg908=
NM_080425.3:c.2724C>G	NP_536350.2:p.Arg908=
NM_080426.2:c.753C>G	NP_536351.1:p.Arg251=
NM_080426.3:c.753C>G	NP_536351.1:p.Arg251=
NR_003259.1:c.-4294966411C>G
XM_017027812.2:c.2727C>G	XP_016883301.1:p.Arg909=
XM_017027813.2:c.2682C>G	XP_016883302.1:p.Arg894=
XM_017027814.2:c.2679C>G	XP_016883303.1:p.Arg893=
XM_017027815.1:c.654C>G	XP_016883304.1:p.Arg218=
XM_017027816.1:c.573C>G	XP_016883305.1:p.Arg191=
XM_017027817.1:c.573C>G	XP_016883306.1:p.Arg191=
XM_017027818.2:c.573C>G	XP_016883307.1:p.Arg191=
XM_017027819.1:c.573C>G	XP_016883308.1:p.Arg191=
XM_017027820.1:c.573C>G	XP_016883309.1:p.Arg191=
XM_024451872.1:c.699C>G	XP_024307640.1:p.Arg233=
XM_024451873.1:c.618C>G	XP_024307641.1:p.Arg206=
XM_024451874.1:c.618C>G	XP_024307642.1:p.Arg206=
XM_024451875.1:c.618C>G	XP_024307643.1:p.Arg206=
XR_002958471.1:n.1502C>G
NM_000516.6:c.795C>G	NP_000507.1:p.Arg265=
NM_001077488.4:c.798C>G	NP_001070956.1:p.Arg266=
NM_001077489.4:c.750C>G	NP_001070957.1:p.Arg250=
NM_001309840.2:c.618C>G	NP_001296769.1:p.Arg206=
NM_001309861.2:c.618C>G	NP_001296790.1:p.Arg206=
NM_016592.4:c.*701C>G	NP_057676.1:n.*701C>G
NM_080426.4:c.753C>G	NP_536351.1:p.Arg251=
NM_000516.7:c.795C>G MANE Select	NP_000507.1:p.Arg265=
NM_001077488.5:c.798C>G	NP_001070956.1:p.Arg266=
NM_001077490.3:c.*656C>G	NP_001070958.1:n.*656C>G
NM_016592.5:c.*701C>G MANE Plus Clinical	NP_057676.1:n.*701C>G
NM_080425.4:c.2724C>G MANE Plus Clinical	NP_536350.2:p.Arg908=