Canonical Allele Identifier: CA2372495571
Gene: GNAS HGNC NCBI
GNAS-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.58840880G= , CM000682.2:g.58840880G= GRCh38
NC_000020.10:g.57415935G= , CM000682.1:g.57415935G= GRCh37
NC_000020.9:g.56849330G= NCBI36
NG_016194.1:g.6141G=
NG_021433.1:g.15024C=
NG_016194.2:g.6141G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419558.7:c.*36G= (GNAS) ENSP00000416234.2:n.*36G=
ENST00000453292.7:c.774G= (GNAS) ENSP00000392000.2:n.774G=
ENST00000306090.12:c.37G= (GNAS) ENSP00000304472.12:p.Asp13=
ENST00000419558.6:c.*36G= (GNAS) ENSP00000416234.2:n.*36G=
ENST00000453292.6:c.*36G= (GNAS) ENSP00000392000.2:n.*36G=
ENST00000657090.1:c.-39+940G= (GNAS) ENSP00000499380.1:n.-39+940G=
ENST00000667293.1:c.4G= (GNAS) ENSP00000499293.1:p.Asp2=
ENST00000313949.11:c.*36G= (GNAS) ENSP00000323571.7:n.*36G=
ENST00000371075.7:c.*36G= (GNAS) MANE Plus Clinical ENSP00000360115.3:n.*36G=
ENST00000371098.6:c.*36G= (GNAS) ENSP00000360139.2:n.*36G=
ENST00000419558.5:c.377G= (GNAS)
ENST00000453292.5:c.537G= (GNAS) ENSP00000392000.1:n.537G=
NM_016592.2:c.*36G= (GNAS) NP_057676.1:n.*36G=
NM_016592.3:c.*36G= (GNAS) NP_057676.1:n.*36G=
NR_002785.2:n.819+1057C= (GNAS-AS1)
XM_017027815.1:c.37G= (GNAS) XP_016883304.1:p.Asp13=
XM_017027821.1:c.*36G= (GNAS) XP_016883310.1:n.*36G=
XM_017027822.1:c.*36G= (GNAS) XP_016883311.1:n.*36G=
XM_024451872.1:c.37G= (GNAS) XP_024307640.1:p.Asp13=
NM_016592.4:c.*36G= (GNAS) NP_057676.1:n.*36G=
NM_016592.5:c.*36G= (GNAS) MANE Plus Clinical NP_057676.1:n.*36G=