Canonical Allele Identifier: CA409453137

Gene: GNAS GNAS-AS1

Linked Data

• MyVariant Identifiers: chr20:g.57415799A>T (hg19) ; chr20:g.58840744A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58840744A>T , CM000682.2:g.58840744A>T	GRCh38
NC_000020.10:g.57415799A>T , CM000682.1:g.57415799A>T	GRCh37
NC_000020.9:g.56849194A>T	NCBI36
NG_016194.1:g.6005A>T
NG_021433.1:g.15160T>A
NG_016194.2:g.6005A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419558.7:c.638A>T (GNAS)	ENSP00000416234.2:p.Glu213Val
ENST00000453292.7:c.638A>T (GNAS)	ENSP00000392000.2:p.Glu213Val
ENST00000419558.6:c.638A>T (GNAS)	ENSP00000416234.2:p.Glu213Val
ENST00000453292.6:c.638A>T (GNAS)	ENSP00000392000.2:p.Glu213Val
ENST00000657090.1:c.-39+804A>T (GNAS)	ENSP00000499380.1:n.-39+804A>T
ENST00000667293.1:c.-27-106A>T (GNAS)	ENSP00000499293.1:n.-27-106A>T
ENST00000313949.11:c.638A>T (GNAS)	ENSP00000323571.7:p.Glu213Val
ENST00000371075.7:c.638A>T (GNAS) MANE Plus Clinical	ENSP00000360115.3:p.Glu213Val
ENST00000371098.6:c.638A>T (GNAS)	ENSP00000360139.2:p.Glu213Val
ENST00000419558.5:c.241A>T (GNAS)
ENST00000453292.5:c.401A>T (GNAS)	ENSP00000392000.1:p.Glu134Val
NM_016592.2:c.638A>T (GNAS)	NP_057676.1:p.Glu213Val
NM_016592.3:c.638A>T (GNAS)	NP_057676.1:p.Glu213Val
NR_002785.2:n.819+1193T>A (GNAS-AS1)
XM_017027821.1:c.638A>T (GNAS)	XP_016883310.1:p.Glu213Val
XM_017027822.1:c.638A>T (GNAS)	XP_016883311.1:p.Glu213Val
XM_024451872.1:c.-100A>T (GNAS)	XP_024307640.1:n.-100A>T
NM_016592.4:c.638A>T (GNAS)	NP_057676.1:p.Glu213Val
NM_016592.5:c.638A>T (GNAS) MANE Plus Clinical	NP_057676.1:p.Glu213Val