Canonical Allele Identifier: CA409452730

Gene: GNAS

Linked Data

• MyVariant Identifiers: chr20:g.57484831A>T (hg19) ; chr20:g.58909776A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58909776A>T , CM000682.2:g.58909776A>T	GRCh38
NC_000020.10:g.57484831A>T , CM000682.1:g.57484831A>T	GRCh37
NC_000020.9:g.56918226A>T	NCBI36
NG_016194.1:g.75037A>T
NG_016194.2:g.75037A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349036.9:c.2695A>T	ENSP00000265621.6:p.Asn899Tyr
ENST00000419558.7:c.*669A>T	ENSP00000416234.2:n.*669A>T
ENST00000453292.7:c.1410A>T	ENSP00000392000.2:n.1410A>T
ENST00000462499.6:c.592A>T	ENSP00000499758.2:p.Asn198Tyr
ENST00000464624.7:c.*653A>T	ENSP00000499607.2:n.*653A>T
ENST00000464788.6:c.634A>T	ENSP00000499239.2:p.Asn212Tyr
ENST00000467227.6:c.592A>T	ENSP00000499681.2:p.Asn198Tyr
ENST00000467321.6:c.634A>T	ENSP00000499523.2:p.Asn212Tyr
ENST00000468895.6:c.811A>T	ENSP00000499551.2:p.Asn271Tyr
ENST00000469431.6:c.634A>T	ENSP00000499654.2:p.Asn212Tyr
ENST00000470512.6:c.637A>T	ENSP00000499552.2:p.Asn213Tyr
ENST00000472183.6:c.634A>T	ENSP00000499673.2:p.Asn212Tyr
ENST00000475610.2:n.1317A>T
ENST00000476935.6:c.589A>T	ENSP00000499409.2:p.Asn197Tyr
ENST00000478585.6:c.592A>T	ENSP00000499762.2:p.Asn198Tyr
ENST00000480232.6:c.637A>T	ENSP00000499545.2:p.Asn213Tyr
ENST00000481039.6:c.592A>T	ENSP00000499767.2:p.Asn198Tyr
ENST00000482112.6:c.589A>T	ENSP00000499794.2:p.Asn197Tyr
ENST00000485673.6:c.592A>T	ENSP00000499334.2:p.Asn198Tyr
ENST00000488546.6:c.592A>T	ENSP00000499332.2:p.Asn198Tyr
ENST00000488652.6:c.634A>T	ENSP00000499435.2:p.Asn212Tyr
ENST00000492907.6:c.592A>T	ENSP00000499443.2:p.Asn198Tyr
ENST00000603546.2:c.634A>T	ENSP00000474802.2:p.Asn212Tyr
ENST00000604005.6:c.634A>T	ENSP00000474219.2:p.Asn212Tyr
ENST00000663479.2:c.637A>T	ENSP00000499353.2:p.Asn213Tyr
ENST00000667293.2:c.634A>T	ENSP00000499293.2:p.Asn212Tyr
ENST00000676826.2:c.2743A>T	ENSP00000504675.2:p.Asn915Tyr
ENST00000682092.1:n.5095A>T
ENST00000682134.1:n.2737A>T
ENST00000682411.1:n.2906A>T
ENST00000682590.1:n.4998A>T
ENST00000682680.1:n.5012A>T
ENST00000682803.1:c.484A>T	ENSP00000507069.1:p.Asn162Tyr
ENST00000682829.1:n.3139A>T
ENST00000682917.1:n.1339A>T
ENST00000682986.1:n.5228A>T
ENST00000683015.1:c.1581A>T	ENSP00000506815.1:n.1581A>T
ENST00000683632.1:n.5341A>T
ENST00000683932.1:n.6587A>T
ENST00000684284.1:n.3189A>T
ENST00000684466.1:n.1450A>T
ENST00000684644.1:n.5131A>T
ENST00000684761.1:n.1304A>T
ENST00000306090.12:c.715A>T	ENSP00000304472.12:p.Asn239Tyr
ENST00000354359.12:c.814A>T	ENSP00000346328.7:p.Asn272Tyr
ENST00000371085.8:c.811A>T MANE Select	ENSP00000360126.3:p.Asn271Tyr
ENST00000371100.9:c.2740A>T MANE Plus Clinical	ENSP00000360141.3:p.Asn914Tyr
ENST00000656419.1:c.340A>T	ENSP00000499614.1:p.Asn114Tyr
ENST00000657090.1:c.634A>T	ENSP00000499380.1:p.Asn212Tyr
ENST00000667293.1:c.682A>T	ENSP00000499293.1:p.Asn228Tyr
ENST00000265620.11:c.766A>T	ENSP00000265620.7:p.Asn256Tyr
ENST00000306090.11:c.103A>T	ENSP00000304472.11:p.Asn35Tyr
ENST00000313949.11:c.*714A>T	ENSP00000323571.7:n.*714A>T
ENST00000354359.11:c.814A>T	ENSP00000346328.7:p.Asn272Tyr
ENST00000371075.7:c.*717A>T MANE Plus Clinical	ENSP00000360115.3:n.*717A>T
ENST00000371085.7:c.811A>T	ENSP00000360126.3:p.Asn271Tyr
ENST00000371095.7:c.769A>T	ENSP00000360136.3:p.Asn257Tyr
ENST00000371100.8:c.2740A>T	ENSP00000360141.3:p.Asn914Tyr
ENST00000371102.8:c.2698A>T	ENSP00000360143.4:p.Asn900Tyr
ENST00000464624.6:n.3027A>T
ENST00000470512.5:n.885A>T
ENST00000476196.5:n.1104A>T
ENST00000476935.5:n.800A>T
ENST00000477931.5:n.926A>T
ENST00000480232.5:n.830A>T
ENST00000480975.5:n.810A>T
ENST00000481039.5:n.728A>T
ENST00000487862.5:n.1045A>T
ENST00000488546.5:n.670A>T
ENST00000488652.5:n.901A>T
ENST00000492907.5:n.762A>T
ENST00000493958.5:n.534A>T
ENST00000494081.5:n.366A>T
ENST00000496934.5:n.2100A>T
NM_000516.4:c.811A>T	NP_000507.1:p.Asn271Tyr
NM_000516.5:c.811A>T	NP_000507.1:p.Asn271Tyr
NM_001077488.2:c.814A>T	NP_001070956.1:p.Asn272Tyr
NM_001077488.3:c.814A>T	NP_001070956.1:p.Asn272Tyr
NM_001077489.2:c.766A>T	NP_001070957.1:p.Asn256Tyr
NM_001077489.3:c.766A>T	NP_001070957.1:p.Asn256Tyr
NM_001077490.1:c.*672A>T	NP_001070958.1:n.*672A>T
NM_001077490.2:c.*672A>T	NP_001070958.1:n.*672A>T
NM_001309840.1:c.634A>T	NP_001296769.1:p.Asn212Tyr
NM_001309861.1:c.634A>T	NP_001296790.1:p.Asn212Tyr
NM_016592.2:c.*717A>T	NP_057676.1:n.*717A>T
NM_016592.3:c.*717A>T	NP_057676.1:n.*717A>T
NM_080425.2:c.2740A>T	NP_536350.2:p.Asn914Tyr
NM_080425.3:c.2740A>T	NP_536350.2:p.Asn914Tyr
NM_080426.2:c.769A>T	NP_536351.1:p.Asn257Tyr
NM_080426.3:c.769A>T	NP_536351.1:p.Asn257Tyr
NR_003259.1:c.-4294966395A>T
XM_017027812.2:c.2743A>T	XP_016883301.1:p.Asn915Tyr
XM_017027813.2:c.2698A>T	XP_016883302.1:p.Asn900Tyr
XM_017027814.2:c.2695A>T	XP_016883303.1:p.Asn899Tyr
XM_017027815.1:c.670A>T	XP_016883304.1:p.Asn224Tyr
XM_017027816.1:c.589A>T	XP_016883305.1:p.Asn197Tyr
XM_017027817.1:c.589A>T	XP_016883306.1:p.Asn197Tyr
XM_017027818.2:c.589A>T	XP_016883307.1:p.Asn197Tyr
XM_017027819.1:c.589A>T	XP_016883308.1:p.Asn197Tyr
XM_017027820.1:c.589A>T	XP_016883309.1:p.Asn197Tyr
XM_024451872.1:c.715A>T	XP_024307640.1:p.Asn239Tyr
XM_024451873.1:c.634A>T	XP_024307641.1:p.Asn212Tyr
XM_024451874.1:c.634A>T	XP_024307642.1:p.Asn212Tyr
XM_024451875.1:c.634A>T	XP_024307643.1:p.Asn212Tyr
XR_002958471.1:n.1518A>T
NM_000516.6:c.811A>T	NP_000507.1:p.Asn271Tyr
NM_001077488.4:c.814A>T	NP_001070956.1:p.Asn272Tyr
NM_001077489.4:c.766A>T	NP_001070957.1:p.Asn256Tyr
NM_001309840.2:c.634A>T	NP_001296769.1:p.Asn212Tyr
NM_001309861.2:c.634A>T	NP_001296790.1:p.Asn212Tyr
NM_016592.4:c.*717A>T	NP_057676.1:n.*717A>T
NM_080426.4:c.769A>T	NP_536351.1:p.Asn257Tyr
NM_000516.7:c.811A>T MANE Select	NP_000507.1:p.Asn271Tyr
NM_001077488.5:c.814A>T	NP_001070956.1:p.Asn272Tyr
NM_001077490.3:c.*672A>T	NP_001070958.1:n.*672A>T
NM_016592.5:c.*717A>T MANE Plus Clinical	NP_057676.1:n.*717A>T
NM_080425.4:c.2740A>T MANE Plus Clinical	NP_536350.2:p.Asn914Tyr