Canonical Allele Identifier: CA2372495418

Gene: GNAS GNAS-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58840582_58840620delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG , CM000682.2:g.58840582_58840620delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG	GRCh38
NC_000020.10:g.57415637_57415675delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG , CM000682.1:g.57415637_57415675delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG	GRCh37
NC_000020.9:g.56849032_56849070delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG	NCBI36
NG_016194.1:g.5843_5881delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG
NG_021433.1:g.15284_15322delinsCGGGGCTTCGCAACTTGAGAGCGTGCAGACGCTGGGTGA
NG_016194.2:g.5843_5881delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419558.7:c.476_514delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	ENSP00000416234.2:p.Leu159=
ENST00000453292.7:c.476_514delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	ENSP00000392000.2:p.Leu159=
ENST00000419558.6:c.476_514delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	ENSP00000416234.2:p.Leu159=
ENST00000453292.6:c.476_514delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	ENSP00000392000.2:p.Leu159=
ENST00000657090.1:c.-39+642_-39+680delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	ENSP00000499380.1:n.-39+642_-39+680delinsTCACCCAGCGTCTGCACGCT...
ENST00000667293.1:c.-27-268_-27-230delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	ENSP00000499293.1:n.-27-268_-27-230delinsTCACCCAGCGTCTGCACGCT...
ENST00000313949.11:c.476_514delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	ENSP00000323571.7:p.Leu159=
ENST00000371075.7:c.476_514delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS) MANE Plus Clinical	ENSP00000360115.3:p.Leu159=
ENST00000371098.6:c.476_514delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	ENSP00000360139.2:p.Leu159=
ENST00000419558.5:c.79_117delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)
ENST00000453292.5:c.239_277delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	ENSP00000392000.1:p.Leu80=
NM_016592.2:c.476_514delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	NP_057676.1:p.Leu159=
NM_016592.3:c.476_514delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	NP_057676.1:p.Leu159=
NR_002785.2:n.819+1317_819+1355delinsCGGGGCTTCGCAACTTGAGAGCGTGCAGACGCTGGGTGA (GNAS-AS1)
XM_017027821.1:c.476_514delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	XP_016883310.1:p.Leu159=
XM_017027822.1:c.476_514delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	XP_016883311.1:p.Leu159=
XM_024451872.1:c.-262_-224delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	XP_024307640.1:n.-262_-224delinsTCACCCAGCGTCTGCACGCTCTCAAGTTG...
NM_016592.4:c.476_514delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS)	NP_057676.1:p.Leu159=
NM_016592.5:c.476_514delinsTCACCCAGCGTCTGCACGCTCTCAAGTTGCGAAGCCCCG (GNAS) MANE Plus Clinical	NP_057676.1:p.Leu159=