Canonical Allele Identifier: CA316327328

Gene: GNAS GNAS-AS1

Linked Data

• dbSNP Id: rs35706121
• MyVariant Identifiers: chr20:g.57415645_57415646insT (hg19) ; chr20:g.58840590_58840591insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58840590_58840591insT , CM000682.2:g.58840590_58840591insT	GRCh38
NC_000020.10:g.57415645_57415646insT , CM000682.1:g.57415645_57415646insT	GRCh37
NC_000020.9:g.56849040_56849041insT	NCBI36
NG_016194.1:g.5851_5852insT
NG_021433.1:g.15313_15314insA
NG_016194.2:g.5851_5852insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419558.7:c.484_485insT (GNAS)	ENSP00000416234.2:p.Arg162LeufsTer?
ENST00000453292.7:c.484_485insT (GNAS)	ENSP00000392000.2:p.Arg162LeufsTer?
ENST00000419558.6:c.484_485insT (GNAS)	ENSP00000416234.2:p.Arg162LeufsTer?
ENST00000453292.6:c.484_485insT (GNAS)	ENSP00000392000.2:p.Arg162LeufsTer?
ENST00000657090.1:c.-39+650_-39+651insT (GNAS)	ENSP00000499380.1:n.-39+650_-39+651insT
ENST00000667293.1:c.-27-260_-27-259insT (GNAS)	ENSP00000499293.1:n.-27-260_-27-259insT
ENST00000313949.11:c.484_485insT (GNAS)	ENSP00000323571.7:p.Arg162LeufsTer?
ENST00000371075.7:c.484_485insT (GNAS) MANE Plus Clinical	ENSP00000360115.3:p.Arg162LeufsTer?
ENST00000371098.6:c.484_485insT (GNAS)	ENSP00000360139.2:p.Arg162LeufsTer?
ENST00000419558.5:c.87_88insT (GNAS)
ENST00000453292.5:c.247_248insT (GNAS)	ENSP00000392000.1:p.Arg83LeufsTer?
NM_016592.2:c.484_485insT (GNAS)	NP_057676.1:p.Arg162LeufsTer?
NM_016592.3:c.484_485insT (GNAS)	NP_057676.1:p.Arg162LeufsTer?
NR_002785.2:n.819+1346_819+1347insA (GNAS-AS1)
XM_017027821.1:c.484_485insT (GNAS)	XP_016883310.1:p.Arg162LeufsTer?
XM_017027822.1:c.484_485insT (GNAS)	XP_016883311.1:p.Arg162LeufsTer?
XM_024451872.1:c.-254_-253insT (GNAS)	XP_024307640.1:n.-254_-253insT
NM_016592.4:c.484_485insT (GNAS)	NP_057676.1:p.Arg162LeufsTer?
NM_016592.5:c.484_485insT (GNAS) MANE Plus Clinical	NP_057676.1:p.Arg162LeufsTer?