Canonical Allele Identifier: CA2372495361

Gene: GNAS GNAS-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58840480_58840516delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC , CM000682.2:g.58840480_58840516delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC	GRCh38
NC_000020.10:g.57415535_57415571delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC , CM000682.1:g.57415535_57415571delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC	GRCh37
NC_000020.9:g.56848930_56848966delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC	NCBI36
NG_016194.1:g.5741_5777delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC
NG_021433.1:g.15388_15424delinsGGCTCAGTGGTGGGGGCGGTCTCAGGCTCGGTCTCGA
NG_016194.2:g.5741_5777delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419558.7:c.374_410delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	ENSP00000416234.2:p.Phe125=
ENST00000453292.7:c.374_410delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	ENSP00000392000.2:p.Phe125=
ENST00000419558.6:c.374_410delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	ENSP00000416234.2:p.Phe125=
ENST00000453292.6:c.374_410delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	ENSP00000392000.2:p.Phe125=
ENST00000657090.1:c.-39+540_-39+576delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	ENSP00000499380.1:n.-39+540_-39+576delinsTCGAGACCGAGCCTGAGACC...
ENST00000667293.1:c.-27-370_-27-334delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	ENSP00000499293.1:n.-27-370_-27-334delinsTCGAGACCGAGCCTGAGACC...
ENST00000313949.11:c.374_410delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	ENSP00000323571.7:p.Phe125=
ENST00000371075.7:c.374_410delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS) MANE Plus Clinical	ENSP00000360115.3:p.Phe125=
ENST00000371098.6:c.374_410delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	ENSP00000360139.2:p.Phe125=
ENST00000453292.5:c.137_173delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	ENSP00000392000.1:p.Phe46=
NM_016592.2:c.374_410delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	NP_057676.1:p.Phe125=
NM_016592.3:c.374_410delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	NP_057676.1:p.Phe125=
NR_002785.2:n.819+1421_819+1457delinsGGCTCAGTGGTGGGGGCGGTCTCAGGCTCGGTCTCGA (GNAS-AS1)
XM_017027821.1:c.374_410delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	XP_016883310.1:p.Phe125=
XM_017027822.1:c.374_410delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	XP_016883311.1:p.Phe125=
XM_024451872.1:c.-364_-328delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	XP_024307640.1:n.-364_-328delinsTCGAGACCGAGCCTGAGACCGCCCCCACC...
NM_016592.4:c.374_410delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS)	NP_057676.1:p.Phe125=
NM_016592.5:c.374_410delinsTCGAGACCGAGCCTGAGACCGCCCCCACCACTGAGCC (GNAS) MANE Plus Clinical	NP_057676.1:p.Phe125=