Canonical Allele Identifier: CA511315994

Gene: GNAS GNAS-AS1

Linked Data

• MyVariant Identifiers: chr20:g.57415608G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58840553G>T , CM000682.2:g.58840553G>T	GRCh38
NC_000020.10:g.57415608G>T , CM000682.1:g.57415608G>T	GRCh37
NC_000020.9:g.56849003G>T	NCBI36
NG_016194.1:g.5814G>T
NG_021433.1:g.15351C>A
NG_016194.2:g.5814G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419558.7:c.447G>T (GNAS)	ENSP00000416234.2:p.Val149=
ENST00000453292.7:c.447G>T (GNAS)	ENSP00000392000.2:p.Val149=
ENST00000419558.6:c.447G>T (GNAS)	ENSP00000416234.2:p.Val149=
ENST00000453292.6:c.447G>T (GNAS)	ENSP00000392000.2:p.Val149=
ENST00000657090.1:c.-39+613G>T (GNAS)	ENSP00000499380.1:n.-39+613G>T
ENST00000667293.1:c.-27-297G>T (GNAS)	ENSP00000499293.1:n.-27-297G>T
ENST00000313949.11:c.447G>T (GNAS)	ENSP00000323571.7:p.Val149=
ENST00000371075.7:c.447G>T (GNAS) MANE Plus Clinical	ENSP00000360115.3:p.Val149=
ENST00000371098.6:c.447G>T (GNAS)	ENSP00000360139.2:p.Val149=
ENST00000419558.5:c.50G>T (GNAS)
ENST00000453292.5:c.210G>T (GNAS)	ENSP00000392000.1:p.Val70=
NM_016592.2:c.447G>T (GNAS)	NP_057676.1:p.Val149=
NM_016592.3:c.447G>T (GNAS)	NP_057676.1:p.Val149=
NR_002785.2:n.819+1384C>A (GNAS-AS1)
XM_017027821.1:c.447G>T (GNAS)	XP_016883310.1:p.Val149=
XM_017027822.1:c.447G>T (GNAS)	XP_016883311.1:p.Val149=
XM_024451872.1:c.-291G>T (GNAS)	XP_024307640.1:n.-291G>T
NM_016592.4:c.447G>T (GNAS)	NP_057676.1:p.Val149=
NM_016592.5:c.447G>T (GNAS) MANE Plus Clinical	NP_057676.1:p.Val149=