Canonical Allele Identifier: CA2372495575

Gene: GNAS GNAS-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58840886G= , CM000682.2:g.58840886G=	GRCh38
NC_000020.10:g.57415941G= , CM000682.1:g.57415941G=	GRCh37
NC_000020.9:g.56849336G=	NCBI36
NG_016194.1:g.6147G=
NG_021433.1:g.15018C=
NG_016194.2:g.6147G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419558.7:c.*42G= (GNAS)	ENSP00000416234.2:n.*42G=
ENST00000453292.7:c.780G= (GNAS)	ENSP00000392000.2:n.780G=
ENST00000306090.12:c.43G= (GNAS)	ENSP00000304472.12:p.Gly15=
ENST00000419558.6:c.*42G= (GNAS)	ENSP00000416234.2:n.*42G=
ENST00000453292.6:c.*42G= (GNAS)	ENSP00000392000.2:n.*42G=
ENST00000657090.1:c.-39+946G= (GNAS)	ENSP00000499380.1:n.-39+946G=
ENST00000667293.1:c.10G= (GNAS)	ENSP00000499293.1:p.Gly4=
ENST00000313949.11:c.*42G= (GNAS)	ENSP00000323571.7:n.*42G=
ENST00000371075.7:c.*42G= (GNAS) MANE Plus Clinical	ENSP00000360115.3:n.*42G=
ENST00000371098.6:c.*42G= (GNAS)	ENSP00000360139.2:n.*42G=
ENST00000419558.5:c.383G= (GNAS)
ENST00000453292.5:c.543G= (GNAS)	ENSP00000392000.1:n.543G=
NM_016592.2:c.*42G= (GNAS)	NP_057676.1:n.*42G=
NM_016592.3:c.*42G= (GNAS)	NP_057676.1:n.*42G=
NR_002785.2:n.819+1051C= (GNAS-AS1)
XM_017027815.1:c.43G= (GNAS)	XP_016883304.1:p.Gly15=
XM_017027821.1:c.*42G= (GNAS)	XP_016883310.1:n.*42G=
XM_017027822.1:c.*42G= (GNAS)	XP_016883311.1:n.*42G=
XM_024451872.1:c.43G= (GNAS)	XP_024307640.1:p.Gly15=
NM_016592.4:c.*42G= (GNAS)	NP_057676.1:n.*42G=
NM_016592.5:c.*42G= (GNAS) MANE Plus Clinical	NP_057676.1:n.*42G=