Canonical Allele Identifier: CA2372495553
Gene: GNAS HGNC NCBI
GNAS-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.58840852C= , CM000682.2:g.58840852C= GRCh38
NC_000020.10:g.57415907C= , CM000682.1:g.57415907C= GRCh37
NC_000020.9:g.56849302C= NCBI36
NG_016194.1:g.6113C=
NG_021433.1:g.15052G=
NG_016194.2:g.6113C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419558.7:c.*8C= (GNAS) ENSP00000416234.2:n.*8C=
ENST00000453292.7:c.746C= (GNAS) ENSP00000392000.2:n.746C=
ENST00000306090.12:c.9C= (GNAS) ENSP00000304472.12:p.Asp3=
ENST00000419558.6:c.*8C= (GNAS) ENSP00000416234.2:n.*8C=
ENST00000453292.6:c.*8C= (GNAS) ENSP00000392000.2:n.*8C=
ENST00000657090.1:c.-39+912C= (GNAS) ENSP00000499380.1:n.-39+912C=
ENST00000667293.1:c.-25C= (GNAS) ENSP00000499293.1:n.-25C=
ENST00000313949.11:c.*8C= (GNAS) ENSP00000323571.7:n.*8C=
ENST00000371075.7:c.*8C= (GNAS) MANE Plus Clinical ENSP00000360115.3:n.*8C=
ENST00000371098.6:c.*8C= (GNAS) ENSP00000360139.2:n.*8C=
ENST00000419558.5:c.349C= (GNAS)
ENST00000453292.5:c.509C= (GNAS) ENSP00000392000.1:n.509C=
NM_016592.2:c.*8C= (GNAS) NP_057676.1:n.*8C=
NM_016592.3:c.*8C= (GNAS) NP_057676.1:n.*8C=
NR_002785.2:n.819+1085G= (GNAS-AS1)
XM_017027815.1:c.9C= (GNAS) XP_016883304.1:p.Asp3=
XM_017027821.1:c.*8C= (GNAS) XP_016883310.1:n.*8C=
XM_017027822.1:c.*8C= (GNAS) XP_016883311.1:n.*8C=
XM_024451872.1:c.9C= (GNAS) XP_024307640.1:p.Asp3=
NM_016592.4:c.*8C= (GNAS) NP_057676.1:n.*8C=
NM_016592.5:c.*8C= (GNAS) MANE Plus Clinical NP_057676.1:n.*8C=