Canonical Allele Identifier: CA409452735

Gene: GNAS

Linked Data

• MyVariant Identifiers: chr20:g.57484832A>G (hg19) ; chr20:g.58909777A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58909777A>G , CM000682.2:g.58909777A>G	GRCh38
NC_000020.10:g.57484832A>G , CM000682.1:g.57484832A>G	GRCh37
NC_000020.9:g.56918227A>G	NCBI36
NG_016194.1:g.75038A>G
NG_016194.2:g.75038A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349036.9:c.2696A>G	ENSP00000265621.6:p.Asn899Ser
ENST00000419558.7:c.*670A>G	ENSP00000416234.2:n.*670A>G
ENST00000453292.7:c.1411A>G	ENSP00000392000.2:n.1411A>G
ENST00000462499.6:c.593A>G	ENSP00000499758.2:p.Asn198Ser
ENST00000464624.7:c.*654A>G	ENSP00000499607.2:n.*654A>G
ENST00000464788.6:c.635A>G	ENSP00000499239.2:p.Asn212Ser
ENST00000467227.6:c.593A>G	ENSP00000499681.2:p.Asn198Ser
ENST00000467321.6:c.635A>G	ENSP00000499523.2:p.Asn212Ser
ENST00000468895.6:c.812A>G	ENSP00000499551.2:p.Asn271Ser
ENST00000469431.6:c.635A>G	ENSP00000499654.2:p.Asn212Ser
ENST00000470512.6:c.638A>G	ENSP00000499552.2:p.Asn213Ser
ENST00000472183.6:c.635A>G	ENSP00000499673.2:p.Asn212Ser
ENST00000475610.2:n.1318A>G
ENST00000476935.6:c.590A>G	ENSP00000499409.2:p.Asn197Ser
ENST00000478585.6:c.593A>G	ENSP00000499762.2:p.Asn198Ser
ENST00000480232.6:c.638A>G	ENSP00000499545.2:p.Asn213Ser
ENST00000481039.6:c.593A>G	ENSP00000499767.2:p.Asn198Ser
ENST00000482112.6:c.590A>G	ENSP00000499794.2:p.Asn197Ser
ENST00000485673.6:c.593A>G	ENSP00000499334.2:p.Asn198Ser
ENST00000488546.6:c.593A>G	ENSP00000499332.2:p.Asn198Ser
ENST00000488652.6:c.635A>G	ENSP00000499435.2:p.Asn212Ser
ENST00000492907.6:c.593A>G	ENSP00000499443.2:p.Asn198Ser
ENST00000603546.2:c.635A>G	ENSP00000474802.2:p.Asn212Ser
ENST00000604005.6:c.635A>G	ENSP00000474219.2:p.Asn212Ser
ENST00000663479.2:c.638A>G	ENSP00000499353.2:p.Asn213Ser
ENST00000667293.2:c.635A>G	ENSP00000499293.2:p.Asn212Ser
ENST00000676826.2:c.2744A>G	ENSP00000504675.2:p.Asn915Ser
ENST00000682092.1:n.5096A>G
ENST00000682134.1:n.2738A>G
ENST00000682411.1:n.2907A>G
ENST00000682590.1:n.4999A>G
ENST00000682680.1:n.5013A>G
ENST00000682803.1:c.485A>G	ENSP00000507069.1:p.Asn162Ser
ENST00000682829.1:n.3140A>G
ENST00000682917.1:n.1340A>G
ENST00000682986.1:n.5229A>G
ENST00000683015.1:c.1582A>G	ENSP00000506815.1:n.1582A>G
ENST00000683632.1:n.5342A>G
ENST00000683932.1:n.6588A>G
ENST00000684284.1:n.3190A>G
ENST00000684466.1:n.1451A>G
ENST00000684644.1:n.5132A>G
ENST00000684761.1:n.1305A>G
ENST00000306090.12:c.716A>G	ENSP00000304472.12:p.Asn239Ser
ENST00000354359.12:c.815A>G	ENSP00000346328.7:p.Asn272Ser
ENST00000371085.8:c.812A>G MANE Select	ENSP00000360126.3:p.Asn271Ser
ENST00000371100.9:c.2741A>G MANE Plus Clinical	ENSP00000360141.3:p.Asn914Ser
ENST00000656419.1:c.341A>G	ENSP00000499614.1:p.Asn114Ser
ENST00000657090.1:c.635A>G	ENSP00000499380.1:p.Asn212Ser
ENST00000667293.1:c.683A>G	ENSP00000499293.1:p.Asn228Ser
ENST00000265620.11:c.767A>G	ENSP00000265620.7:p.Asn256Ser
ENST00000306090.11:c.104A>G	ENSP00000304472.11:p.Asn35Ser
ENST00000313949.11:c.*715A>G	ENSP00000323571.7:n.*715A>G
ENST00000354359.11:c.815A>G	ENSP00000346328.7:p.Asn272Ser
ENST00000371075.7:c.*718A>G MANE Plus Clinical	ENSP00000360115.3:n.*718A>G
ENST00000371085.7:c.812A>G	ENSP00000360126.3:p.Asn271Ser
ENST00000371095.7:c.770A>G	ENSP00000360136.3:p.Asn257Ser
ENST00000371100.8:c.2741A>G	ENSP00000360141.3:p.Asn914Ser
ENST00000371102.8:c.2699A>G	ENSP00000360143.4:p.Asn900Ser
ENST00000464624.6:n.3028A>G
ENST00000470512.5:n.886A>G
ENST00000476196.5:n.1105A>G
ENST00000476935.5:n.801A>G
ENST00000477931.5:n.927A>G
ENST00000480232.5:n.831A>G
ENST00000480975.5:n.811A>G
ENST00000481039.5:n.729A>G
ENST00000487862.5:n.1046A>G
ENST00000488546.5:n.671A>G
ENST00000488652.5:n.902A>G
ENST00000492907.5:n.763A>G
ENST00000494081.5:n.367A>G
ENST00000496934.5:n.2101A>G
NM_000516.4:c.812A>G	NP_000507.1:p.Asn271Ser
NM_000516.5:c.812A>G	NP_000507.1:p.Asn271Ser
NM_001077488.2:c.815A>G	NP_001070956.1:p.Asn272Ser
NM_001077488.3:c.815A>G	NP_001070956.1:p.Asn272Ser
NM_001077489.2:c.767A>G	NP_001070957.1:p.Asn256Ser
NM_001077489.3:c.767A>G	NP_001070957.1:p.Asn256Ser
NM_001077490.1:c.*673A>G	NP_001070958.1:n.*673A>G
NM_001077490.2:c.*673A>G	NP_001070958.1:n.*673A>G
NM_001309840.1:c.635A>G	NP_001296769.1:p.Asn212Ser
NM_001309861.1:c.635A>G	NP_001296790.1:p.Asn212Ser
NM_016592.2:c.*718A>G	NP_057676.1:n.*718A>G
NM_016592.3:c.*718A>G	NP_057676.1:n.*718A>G
NM_080425.2:c.2741A>G	NP_536350.2:p.Asn914Ser
NM_080425.3:c.2741A>G	NP_536350.2:p.Asn914Ser
NM_080426.2:c.770A>G	NP_536351.1:p.Asn257Ser
NM_080426.3:c.770A>G	NP_536351.1:p.Asn257Ser
NR_003259.1:c.-4294966394A>G
XM_017027812.2:c.2744A>G	XP_016883301.1:p.Asn915Ser
XM_017027813.2:c.2699A>G	XP_016883302.1:p.Asn900Ser
XM_017027814.2:c.2696A>G	XP_016883303.1:p.Asn899Ser
XM_017027815.1:c.671A>G	XP_016883304.1:p.Asn224Ser
XM_017027816.1:c.590A>G	XP_016883305.1:p.Asn197Ser
XM_017027817.1:c.590A>G	XP_016883306.1:p.Asn197Ser
XM_017027818.2:c.590A>G	XP_016883307.1:p.Asn197Ser
XM_017027819.1:c.590A>G	XP_016883308.1:p.Asn197Ser
XM_017027820.1:c.590A>G	XP_016883309.1:p.Asn197Ser
XM_024451872.1:c.716A>G	XP_024307640.1:p.Asn239Ser
XM_024451873.1:c.635A>G	XP_024307641.1:p.Asn212Ser
XM_024451874.1:c.635A>G	XP_024307642.1:p.Asn212Ser
XM_024451875.1:c.635A>G	XP_024307643.1:p.Asn212Ser
XR_002958471.1:n.1519A>G
NM_000516.6:c.812A>G	NP_000507.1:p.Asn271Ser
NM_001077488.4:c.815A>G	NP_001070956.1:p.Asn272Ser
NM_001077489.4:c.767A>G	NP_001070957.1:p.Asn256Ser
NM_001309840.2:c.635A>G	NP_001296769.1:p.Asn212Ser
NM_001309861.2:c.635A>G	NP_001296790.1:p.Asn212Ser
NM_016592.4:c.*718A>G	NP_057676.1:n.*718A>G
NM_080426.4:c.770A>G	NP_536351.1:p.Asn257Ser
NM_000516.7:c.812A>G MANE Select	NP_000507.1:p.Asn271Ser
NM_001077488.5:c.815A>G	NP_001070956.1:p.Asn272Ser
NM_001077490.3:c.*673A>G	NP_001070958.1:n.*673A>G
NM_016592.5:c.*718A>G MANE Plus Clinical	NP_057676.1:n.*718A>G
NM_080425.4:c.2741A>G MANE Plus Clinical	NP_536350.2:p.Asn914Ser