Canonical Allele Identifier: CA2372495506
Gene: GNAS HGNC NCBI
GNAS-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.58840752C= , CM000682.2:g.58840752C= GRCh38
NC_000020.10:g.57415807C= , CM000682.1:g.57415807C= GRCh37
NC_000020.9:g.56849202C= NCBI36
NG_016194.1:g.6013C=
NG_021433.1:g.15152G=
NG_016194.2:g.6013C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419558.7:c.646C= (GNAS) ENSP00000416234.2:p.Arg216=
ENST00000453292.7:c.646C= (GNAS) ENSP00000392000.2:p.Arg216=
ENST00000419558.6:c.646C= (GNAS) ENSP00000416234.2:p.Arg216=
ENST00000453292.6:c.646C= (GNAS) ENSP00000392000.2:p.Arg216=
ENST00000657090.1:c.-39+812C= (GNAS) ENSP00000499380.1:n.-39+812C=
ENST00000667293.1:c.-27-98C= (GNAS) ENSP00000499293.1:n.-27-98C=
ENST00000313949.11:c.646C= (GNAS) ENSP00000323571.7:p.Arg216=
ENST00000371075.7:c.646C= (GNAS) MANE Plus Clinical ENSP00000360115.3:p.Arg216=
ENST00000371098.6:c.646C= (GNAS) ENSP00000360139.2:p.Arg216=
ENST00000419558.5:c.249C= (GNAS)
ENST00000453292.5:c.409C= (GNAS) ENSP00000392000.1:p.Arg137=
NM_016592.2:c.646C= (GNAS) NP_057676.1:p.Arg216=
NM_016592.3:c.646C= (GNAS) NP_057676.1:p.Arg216=
NR_002785.2:n.819+1185G= (GNAS-AS1)
XM_017027821.1:c.646C= (GNAS) XP_016883310.1:p.Arg216=
XM_017027822.1:c.646C= (GNAS) XP_016883311.1:p.Arg216=
XM_024451872.1:c.-92C= (GNAS) XP_024307640.1:n.-92C=
NM_016592.4:c.646C= (GNAS) NP_057676.1:p.Arg216=
NM_016592.5:c.646C= (GNAS) MANE Plus Clinical NP_057676.1:p.Arg216=