Canonical Allele Identifier: CA2372495490
Gene: GNAS HGNC NCBI
GNAS-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.58840724G= , CM000682.2:g.58840724G= GRCh38
NC_000020.10:g.57415779G= , CM000682.1:g.57415779G= GRCh37
NC_000020.9:g.56849174G= NCBI36
NG_016194.1:g.5985G=
NG_021433.1:g.15180C=
NG_016194.2:g.5985G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419558.7:c.618G= (GNAS) ENSP00000416234.2:p.Glu206=
ENST00000453292.7:c.618G= (GNAS) ENSP00000392000.2:p.Glu206=
ENST00000419558.6:c.618G= (GNAS) ENSP00000416234.2:p.Glu206=
ENST00000453292.6:c.618G= (GNAS) ENSP00000392000.2:p.Glu206=
ENST00000657090.1:c.-39+784G= (GNAS) ENSP00000499380.1:n.-39+784G=
ENST00000667293.1:c.-27-126G= (GNAS) ENSP00000499293.1:n.-27-126G=
ENST00000313949.11:c.618G= (GNAS) ENSP00000323571.7:p.Glu206=
ENST00000371075.7:c.618G= (GNAS) MANE Plus Clinical ENSP00000360115.3:p.Glu206=
ENST00000371098.6:c.618G= (GNAS) ENSP00000360139.2:p.Glu206=
ENST00000419558.5:c.221G= (GNAS)
ENST00000453292.5:c.381G= (GNAS) ENSP00000392000.1:p.Glu127=
NM_016592.2:c.618G= (GNAS) NP_057676.1:p.Glu206=
NM_016592.3:c.618G= (GNAS) NP_057676.1:p.Glu206=
NR_002785.2:n.819+1213C= (GNAS-AS1)
XM_017027821.1:c.618G= (GNAS) XP_016883310.1:p.Glu206=
XM_017027822.1:c.618G= (GNAS) XP_016883311.1:p.Glu206=
XM_024451872.1:c.-120G= (GNAS) XP_024307640.1:n.-120G=
NM_016592.4:c.618G= (GNAS) NP_057676.1:p.Glu206=
NM_016592.5:c.618G= (GNAS) MANE Plus Clinical NP_057676.1:p.Glu206=