Canonical Allele Identifier: CA409455990

Gene: GNAS

Linked Data

• ClinVar Variation Id: 431104
• ClinVar RCV Id: RCV003313085
• dbSNP Id: rs1135401777
• gnomAD v3: 20-58853740-G-A
• gnomAD v4: 20-58853740-G-A
• MyVariant Identifiers: chr20:g.57428795G>A (hg19) ; chr20:g.58853740G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58853740G>A , CM000682.2:g.58853740G>A	GRCh38
NC_000020.10:g.57428795G>A , CM000682.1:g.57428795G>A	GRCh37
NC_000020.9:g.56862190G>A	NCBI36
NG_016194.1:g.19001G>A
NG_021433.1:g.2164C>T
NG_016194.2:g.19001G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000349036.9:c.475G>A	ENSP00000265621.6:p.Glu159Lys
ENST00000419558.7:c.*42+12854G>A	ENSP00000416234.2:n.*42+12854G>A
ENST00000423897.7:c.475G>A	ENSP00000412356.2:p.Glu159Lys
ENST00000453292.7:c.780+12854G>A	ENSP00000392000.2:n.780+12854G>A
ENST00000462499.6:c.-39+11865G>A	ENSP00000499758.2:n.-39+11865G>A
ENST00000464624.7:c.475G>A	ENSP00000499607.2:p.Glu159Lys
ENST00000467227.6:c.-39+9666G>A	ENSP00000499681.2:n.-39+9666G>A
ENST00000472183.6:c.-39+11865G>A	ENSP00000499673.2:n.-39+11865G>A
ENST00000482112.6:c.-39+11865G>A	ENSP00000499794.2:n.-39+11865G>A
ENST00000663479.2:c.-39+11865G>A	ENSP00000499353.2:n.-39+11865G>A
ENST00000676826.2:c.475G>A	ENSP00000504675.2:p.Glu159Lys
ENST00000306090.12:c.43+12854G>A	ENSP00000304472.12:n.43+12854G>A
ENST00000306120.4:c.480G>A	ENSP00000302237.4:p.Gln160=
ENST00000349036.8:c.475G>A	ENSP00000265621.5:p.Glu159Lys
ENST00000371100.9:c.475G>A MANE Plus Clinical	ENSP00000360141.3:p.Glu159Lys
ENST00000419558.6:c.*42+12854G>A	ENSP00000416234.2:n.*42+12854G>A
ENST00000423897.6:c.475G>A	ENSP00000412356.2:p.Glu159Lys
ENST00000453292.6:c.*42+12854G>A	ENSP00000392000.2:n.*42+12854G>A
ENST00000481768.6:c.475G>A	ENSP00000499644.2:p.Glu159Lys
ENST00000490374.6:n.222+11865G>A
ENST00000657090.1:c.-39+13800G>A	ENSP00000499380.1:n.-39+13800G>A
ENST00000663479.1:c.-39+11865G>A	ENSP00000499353.1:n.-39+11865G>A
ENST00000667293.1:c.10+12854G>A	ENSP00000499293.1:n.10+12854G>A
ENST00000676826.1:c.475G>A	ENSP00000504675.1:p.Glu159Lys
ENST00000306120.3:c.285G>A	ENSP00000302237.3:p.Gln95=
ENST00000313949.11:c.*42+12854G>A	ENSP00000323571.7:n.*42+12854G>A
ENST00000371075.7:c.*42+12854G>A MANE Plus Clinical	ENSP00000360115.3:n.*42+12854G>A
ENST00000371098.6:c.*42+12854G>A	ENSP00000360139.2:n.*42+12854G>A
ENST00000371099.6:c.475G>A	ENSP00000360140.2:p.Glu159Lys
ENST00000371100.8:c.475G>A	ENSP00000360141.3:p.Glu159Lys
ENST00000371102.8:c.475G>A	ENSP00000360143.4:p.Glu159Lys
ENST00000419558.5:c.383+12854G>A
ENST00000453292.5:c.543+12854G>A	ENSP00000392000.1:n.543+12854G>A
ENST00000462499.5:n.258+11865G>A
ENST00000464624.6:n.478G>A
ENST00000467227.5:n.122+9666G>A
ENST00000472183.5:n.391+11865G>A
ENST00000482112.5:n.258+11865G>A
ENST00000490374.5:n.254+11865G>A
ENST00000491348.5:n.533+11865G>A
ENST00000493744.5:n.232+11865G>A
NM_001077490.1:c.288G>A	NP_001070958.1:p.Gln96=
NM_001077490.2:c.288G>A	NP_001070958.1:p.Gln96=
NM_001309861.1:c.-39+11865G>A	NP_001296790.1:n.-39+11865G>A
NM_001309883.1:c.288G>A	NP_001296812.1:p.Gln96=
NM_016592.2:c.*42+12854G>A	NP_057676.1:n.*42+12854G>A
NM_016592.3:c.*42+12854G>A	NP_057676.1:n.*42+12854G>A
NM_080425.2:c.475G>A	NP_536350.2:p.Glu159Lys
NM_080425.3:c.475G>A	NP_536350.2:p.Glu159Lys
XM_017027812.2:c.475G>A	XP_016883301.1:p.Glu159Lys
XM_017027813.2:c.475G>A	XP_016883302.1:p.Glu159Lys
XM_017027814.2:c.475G>A	XP_016883303.1:p.Glu159Lys
XM_017027815.1:c.43+12854G>A	XP_016883304.1:n.43+12854G>A
XM_017027821.1:c.*42+12854G>A	XP_016883310.1:n.*42+12854G>A
XM_017027822.1:c.*42+12854G>A	XP_016883311.1:n.*42+12854G>A
XM_024451872.1:c.43+12854G>A	XP_024307640.1:n.43+12854G>A
NM_001309861.2:c.-39+11865G>A	NP_001296790.1:n.-39+11865G>A
NM_016592.4:c.*42+12854G>A	NP_057676.1:n.*42+12854G>A
NM_001077490.3:c.288G>A	NP_001070958.1:p.Gln96=
NM_016592.5:c.*42+12854G>A MANE Plus Clinical	NP_057676.1:n.*42+12854G>A
NM_080425.4:c.475G>A MANE Plus Clinical	NP_536350.2:p.Glu159Lys