Canonical Allele Identifier: CA2372529385
Gene: GNAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.58909795G= , CM000682.2:g.58909795G= GRCh38
NC_000020.10:g.57484850G= , CM000682.1:g.57484850G= GRCh37
NC_000020.9:g.56918245G= NCBI36
NG_016194.1:g.75056G=
NG_016194.2:g.75056G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000349036.9:c.2714G= ENSP00000265621.6:p.Trp905=
ENST00000419558.7:c.*688G= ENSP00000416234.2:n.*688G=
ENST00000453292.7:c.1429G= ENSP00000392000.2:n.1429G=
ENST00000462499.6:c.611G= ENSP00000499758.2:p.Trp204=
ENST00000464624.7:c.*672G= ENSP00000499607.2:n.*672G=
ENST00000464788.6:c.653G= ENSP00000499239.2:p.Trp218=
ENST00000467227.6:c.611G= ENSP00000499681.2:p.Trp204=
ENST00000467321.6:c.653G= ENSP00000499523.2:p.Trp218=
ENST00000468895.6:c.830G= ENSP00000499551.2:p.Trp277=
ENST00000469431.6:c.653G= ENSP00000499654.2:p.Trp218=
ENST00000470512.6:c.656G= ENSP00000499552.2:p.Trp219=
ENST00000472183.6:c.653G= ENSP00000499673.2:p.Trp218=
ENST00000475610.2:n.1336G=
ENST00000476935.6:c.608G= ENSP00000499409.2:p.Trp203=
ENST00000478585.6:c.611G= ENSP00000499762.2:p.Trp204=
ENST00000480232.6:c.656G= ENSP00000499545.2:p.Trp219=
ENST00000481039.6:c.611G= ENSP00000499767.2:p.Trp204=
ENST00000482112.6:c.608G= ENSP00000499794.2:p.Trp203=
ENST00000485673.6:c.611G= ENSP00000499334.2:p.Trp204=
ENST00000488546.6:c.611G= ENSP00000499332.2:p.Trp204=
ENST00000488652.6:c.653G= ENSP00000499435.2:p.Trp218=
ENST00000492907.6:c.611G= ENSP00000499443.2:p.Trp204=
ENST00000603546.2:c.653G= ENSP00000474802.2:p.Trp218=
ENST00000604005.6:c.653G= ENSP00000474219.2:p.Trp218=
ENST00000663479.2:c.656G= ENSP00000499353.2:p.Trp219=
ENST00000667293.2:c.653G= ENSP00000499293.2:p.Trp218=
ENST00000676826.2:c.2762G= ENSP00000504675.2:p.Trp921=
ENST00000682092.1:n.5114G=
ENST00000682134.1:n.2756G=
ENST00000682411.1:n.2925G=
ENST00000682590.1:n.5017G=
ENST00000682680.1:n.5031G=
ENST00000682803.1:c.503G= ENSP00000507069.1:p.Trp168=
ENST00000682829.1:n.3158G=
ENST00000682917.1:n.1358G=
ENST00000682986.1:n.5247G=
ENST00000683015.1:c.1600G= ENSP00000506815.1:n.1600G=
ENST00000683632.1:n.5360G=
ENST00000683932.1:n.6606G=
ENST00000684284.1:n.3208G=
ENST00000684466.1:n.1469G=
ENST00000684644.1:n.5150G=
ENST00000684761.1:n.1323G=
ENST00000306090.12:c.734G= ENSP00000304472.12:p.Trp245=
ENST00000354359.12:c.833G= ENSP00000346328.7:p.Trp278=
ENST00000371085.8:c.830G= MANE Select ENSP00000360126.3:p.Trp277=
ENST00000371100.9:c.2759G= MANE Plus Clinical ENSP00000360141.3:p.Trp920=
ENST00000656419.1:c.359G= ENSP00000499614.1:p.Trp120=
ENST00000657090.1:c.653G= ENSP00000499380.1:p.Trp218=
ENST00000667293.1:c.701G= ENSP00000499293.1:p.Trp234=
ENST00000265620.11:c.785G= ENSP00000265620.7:p.Trp262=
ENST00000306090.11:c.122G= ENSP00000304472.11:p.Trp41=
ENST00000313949.11:c.*733G= ENSP00000323571.7:n.*733G=
ENST00000354359.11:c.833G= ENSP00000346328.7:p.Trp278=
ENST00000371075.7:c.*736G= MANE Plus Clinical ENSP00000360115.3:n.*736G=
ENST00000371085.7:c.830G= ENSP00000360126.3:p.Trp277=
ENST00000371095.7:c.788G= ENSP00000360136.3:p.Trp263=
ENST00000371100.8:c.2759G= ENSP00000360141.3:p.Trp920=
ENST00000371102.8:c.2717G= ENSP00000360143.4:p.Trp906=
ENST00000464624.6:n.3046G=
ENST00000470512.5:n.904G=
ENST00000476196.5:n.1123G=
ENST00000476935.5:n.819G=
ENST00000477931.5:n.945G=
ENST00000480232.5:n.849G=
ENST00000480975.5:n.829G=
ENST00000481039.5:n.747G=
ENST00000487862.5:n.1064G=
ENST00000488546.5:n.689G=
ENST00000488652.5:n.920G=
ENST00000492907.5:n.781G=
ENST00000494081.5:n.385G=
ENST00000496934.5:n.2119G=
NM_000516.4:c.830G= NP_000507.1:p.Trp277=
NM_000516.5:c.830G= NP_000507.1:p.Trp277=
NM_001077488.2:c.833G= NP_001070956.1:p.Trp278=
NM_001077488.3:c.833G= NP_001070956.1:p.Trp278=
NM_001077489.2:c.785G= NP_001070957.1:p.Trp262=
NM_001077489.3:c.785G= NP_001070957.1:p.Trp262=
NM_001077490.1:c.*691G= NP_001070958.1:n.*691G=
NM_001077490.2:c.*691G= NP_001070958.1:n.*691G=
NM_001309840.1:c.653G= NP_001296769.1:p.Trp218=
NM_001309861.1:c.653G= NP_001296790.1:p.Trp218=
NM_016592.2:c.*736G= NP_057676.1:n.*736G=
NM_016592.3:c.*736G= NP_057676.1:n.*736G=
NM_080425.2:c.2759G= NP_536350.2:p.Trp920=
NM_080425.3:c.2759G= NP_536350.2:p.Trp920=
NM_080426.2:c.788G= NP_536351.1:p.Trp263=
NM_080426.3:c.788G= NP_536351.1:p.Trp263=
NR_003259.1:c.-4294966376G=
XM_017027812.2:c.2762G= XP_016883301.1:p.Trp921=
XM_017027813.2:c.2717G= XP_016883302.1:p.Trp906=
XM_017027814.2:c.2714G= XP_016883303.1:p.Trp905=
XM_017027815.1:c.689G= XP_016883304.1:p.Trp230=
XM_017027816.1:c.608G= XP_016883305.1:p.Trp203=
XM_017027817.1:c.608G= XP_016883306.1:p.Trp203=
XM_017027818.2:c.608G= XP_016883307.1:p.Trp203=
XM_017027819.1:c.608G= XP_016883308.1:p.Trp203=
XM_017027820.1:c.608G= XP_016883309.1:p.Trp203=
XM_024451872.1:c.734G= XP_024307640.1:p.Trp245=
XM_024451873.1:c.653G= XP_024307641.1:p.Trp218=
XM_024451874.1:c.653G= XP_024307642.1:p.Trp218=
XM_024451875.1:c.653G= XP_024307643.1:p.Trp218=
XR_002958471.1:n.1537G=
NM_000516.6:c.830G= NP_000507.1:p.Trp277=
NM_001077488.4:c.833G= NP_001070956.1:p.Trp278=
NM_001077489.4:c.785G= NP_001070957.1:p.Trp262=
NM_001309840.2:c.653G= NP_001296769.1:p.Trp218=
NM_001309861.2:c.653G= NP_001296790.1:p.Trp218=
NM_016592.4:c.*736G= NP_057676.1:n.*736G=
NM_080426.4:c.788G= NP_536351.1:p.Trp263=
NM_000516.7:c.830G= MANE Select NP_000507.1:p.Trp277=
NM_001077488.5:c.833G= NP_001070956.1:p.Trp278=
NM_001077490.3:c.*691G= NP_001070958.1:n.*691G=
NM_016592.5:c.*736G= MANE Plus Clinical NP_057676.1:n.*736G=
NM_080425.4:c.2759G= MANE Plus Clinical NP_536350.2:p.Trp920=