Canonical Allele Identifier: CA511316110

Gene: GNAS GNAS-AS1

Linked Data

• MyVariant Identifiers: chr20:g.57415854G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58840799G>A , CM000682.2:g.58840799G>A	GRCh38
NC_000020.10:g.57415854G>A , CM000682.1:g.57415854G>A	GRCh37
NC_000020.9:g.56849249G>A	NCBI36
NG_016194.1:g.6060G>A
NG_021433.1:g.15105C>T
NG_016194.2:g.6060G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419558.7:c.693G>A (GNAS)	ENSP00000416234.2:p.Pro231=
ENST00000453292.7:c.693G>A (GNAS)	ENSP00000392000.2:p.Pro231=
ENST00000419558.6:c.693G>A (GNAS)	ENSP00000416234.2:p.Pro231=
ENST00000453292.6:c.693G>A (GNAS)	ENSP00000392000.2:p.Pro231=
ENST00000657090.1:c.-39+859G>A (GNAS)	ENSP00000499380.1:n.-39+859G>A
ENST00000667293.1:c.-27-51G>A (GNAS)	ENSP00000499293.1:n.-27-51G>A
ENST00000313949.11:c.693G>A (GNAS)	ENSP00000323571.7:p.Pro231=
ENST00000371075.7:c.693G>A (GNAS) MANE Plus Clinical	ENSP00000360115.3:p.Pro231=
ENST00000371098.6:c.693G>A (GNAS)	ENSP00000360139.2:p.Pro231=
ENST00000419558.5:c.296G>A (GNAS)
ENST00000453292.5:c.456G>A (GNAS)	ENSP00000392000.1:p.Pro152=
NM_016592.2:c.693G>A (GNAS)	NP_057676.1:p.Pro231=
NM_016592.3:c.693G>A (GNAS)	NP_057676.1:p.Pro231=
NR_002785.2:n.819+1138C>T (GNAS-AS1)
XM_017027815.1:c.-45G>A (GNAS)	XP_016883304.1:n.-45G>A
XM_017027821.1:c.693G>A (GNAS)	XP_016883310.1:p.Pro231=
XM_017027822.1:c.693G>A (GNAS)	XP_016883311.1:p.Pro231=
XM_024451872.1:c.-45G>A (GNAS)	XP_024307640.1:n.-45G>A
NM_016592.4:c.693G>A (GNAS)	NP_057676.1:p.Pro231=
NM_016592.5:c.693G>A (GNAS) MANE Plus Clinical	NP_057676.1:p.Pro231=