Canonical Allele Identifier: CA2372495681
Gene: GNAS HGNC NCBI
GNAS-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.58841088_58841089delinsAG , CM000682.2:g.58841088_58841089delinsAG GRCh38
NC_000020.10:g.57416143_57416144delinsAG , CM000682.1:g.57416143_57416144delinsAG GRCh37
NC_000020.9:g.56849538_56849539delinsAG NCBI36
NG_016194.1:g.6349_6350delinsAG
NG_021433.1:g.14815_14816delinsCT
NG_016194.2:g.6349_6350delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000419558.7:c.*42+202_*42+203delinsAG (GNAS) ENSP00000416234.2:n.*42+202_*42+203delinsAG
ENST00000453292.7:c.780+202_780+203delinsAG (GNAS) ENSP00000392000.2:n.780+202_780+203delinsAG
ENST00000306090.12:c.43+202_43+203delinsAG (GNAS) ENSP00000304472.12:n.43+202_43+203delinsAG
ENST00000419558.6:c.*42+202_*42+203delinsAG (GNAS) ENSP00000416234.2:n.*42+202_*42+203delinsAG
ENST00000453292.6:c.*42+202_*42+203delinsAG (GNAS) ENSP00000392000.2:n.*42+202_*42+203delinsAG
ENST00000657090.1:c.-39+1148_-39+1149delinsAG (GNAS) ENSP00000499380.1:n.-39+1148_-39+1149delinsAG
ENST00000667293.1:c.10+202_10+203delinsAG (GNAS) ENSP00000499293.1:n.10+202_10+203delinsAG
ENST00000313949.11:c.*42+202_*42+203delinsAG (GNAS) ENSP00000323571.7:n.*42+202_*42+203delinsAG
ENST00000371075.7:c.*42+202_*42+203delinsAG (GNAS) MANE Plus Clinical ENSP00000360115.3:n.*42+202_*42+203delinsAG
ENST00000371098.6:c.*42+202_*42+203delinsAG (GNAS) ENSP00000360139.2:n.*42+202_*42+203delinsAG
ENST00000419558.5:c.383+202_383+203delinsAG (GNAS)
ENST00000453292.5:c.543+202_543+203delinsAG (GNAS) ENSP00000392000.1:n.543+202_543+203delinsAG
NM_016592.2:c.*42+202_*42+203delinsAG (GNAS) NP_057676.1:n.*42+202_*42+203delinsAG
NM_016592.3:c.*42+202_*42+203delinsAG (GNAS) NP_057676.1:n.*42+202_*42+203delinsAG
NR_002785.2:n.819+848_819+849delinsCT (GNAS-AS1)
XM_017027815.1:c.43+202_43+203delinsAG (GNAS) XP_016883304.1:n.43+202_43+203delinsAG
XM_017027821.1:c.*42+202_*42+203delinsAG (GNAS) XP_016883310.1:n.*42+202_*42+203delinsAG
XM_017027822.1:c.*42+202_*42+203delinsAG (GNAS) XP_016883311.1:n.*42+202_*42+203delinsAG
XM_024451872.1:c.43+202_43+203delinsAG (GNAS) XP_024307640.1:n.43+202_43+203delinsAG
NM_016592.4:c.*42+202_*42+203delinsAG (GNAS) NP_057676.1:n.*42+202_*42+203delinsAG
NM_016592.5:c.*42+202_*42+203delinsAG (GNAS) MANE Plus Clinical NP_057676.1:n.*42+202_*42+203delinsAG