Canonical Allele Identifier: CA2372495402

Gene: GNAS GNAS-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58840553G= , CM000682.2:g.58840553G=	GRCh38
NC_000020.10:g.57415608G= , CM000682.1:g.57415608G=	GRCh37
NC_000020.9:g.56849003G=	NCBI36
NG_016194.1:g.5814G=
NG_021433.1:g.15351C=
NG_016194.2:g.5814G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419558.7:c.447G= (GNAS)	ENSP00000416234.2:p.Val149=
ENST00000453292.7:c.447G= (GNAS)	ENSP00000392000.2:p.Val149=
ENST00000419558.6:c.447G= (GNAS)	ENSP00000416234.2:p.Val149=
ENST00000453292.6:c.447G= (GNAS)	ENSP00000392000.2:p.Val149=
ENST00000657090.1:c.-39+613G= (GNAS)	ENSP00000499380.1:n.-39+613G=
ENST00000667293.1:c.-27-297G= (GNAS)	ENSP00000499293.1:n.-27-297G=
ENST00000313949.11:c.447G= (GNAS)	ENSP00000323571.7:p.Val149=
ENST00000371075.7:c.447G= (GNAS) MANE Plus Clinical	ENSP00000360115.3:p.Val149=
ENST00000371098.6:c.447G= (GNAS)	ENSP00000360139.2:p.Val149=
ENST00000419558.5:c.50G= (GNAS)
ENST00000453292.5:c.210G= (GNAS)	ENSP00000392000.1:p.Val70=
NM_016592.2:c.447G= (GNAS)	NP_057676.1:p.Val149=
NM_016592.3:c.447G= (GNAS)	NP_057676.1:p.Val149=
NR_002785.2:n.819+1384C= (GNAS-AS1)
XM_017027821.1:c.447G= (GNAS)	XP_016883310.1:p.Val149=
XM_017027822.1:c.447G= (GNAS)	XP_016883311.1:p.Val149=
XM_024451872.1:c.-291G= (GNAS)	XP_024307640.1:n.-291G=
NM_016592.4:c.447G= (GNAS)	NP_057676.1:p.Val149=
NM_016592.5:c.447G= (GNAS) MANE Plus Clinical	NP_057676.1:p.Val149=