Canonical Allele Identifier: CA409451886

Gene: GNAS GNAS-AS1

Linked Data

• MyVariant Identifiers: chr20:g.57415644G>C (hg19) ; chr20:g.58840589G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58840589G>C , CM000682.2:g.58840589G>C	GRCh38
NC_000020.10:g.57415644G>C , CM000682.1:g.57415644G>C	GRCh37
NC_000020.9:g.56849039G>C	NCBI36
NG_016194.1:g.5850G>C
NG_021433.1:g.15315C>G
NG_016194.2:g.5850G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419558.7:c.483G>C (GNAS)	ENSP00000416234.2:p.Gln161His
ENST00000453292.7:c.483G>C (GNAS)	ENSP00000392000.2:p.Gln161His
ENST00000419558.6:c.483G>C (GNAS)	ENSP00000416234.2:p.Gln161His
ENST00000453292.6:c.483G>C (GNAS)	ENSP00000392000.2:p.Gln161His
ENST00000657090.1:c.-39+649G>C (GNAS)	ENSP00000499380.1:n.-39+649G>C
ENST00000667293.1:c.-27-261G>C (GNAS)	ENSP00000499293.1:n.-27-261G>C
ENST00000313949.11:c.483G>C (GNAS)	ENSP00000323571.7:p.Gln161His
ENST00000371075.7:c.483G>C (GNAS) MANE Plus Clinical	ENSP00000360115.3:p.Gln161His
ENST00000371098.6:c.483G>C (GNAS)	ENSP00000360139.2:p.Gln161His
ENST00000419558.5:c.86G>C (GNAS)
ENST00000453292.5:c.246G>C (GNAS)	ENSP00000392000.1:p.Gln82His
NM_016592.2:c.483G>C (GNAS)	NP_057676.1:p.Gln161His
NM_016592.3:c.483G>C (GNAS)	NP_057676.1:p.Gln161His
NR_002785.2:n.819+1348C>G (GNAS-AS1)
XM_017027821.1:c.483G>C (GNAS)	XP_016883310.1:p.Gln161His
XM_017027822.1:c.483G>C (GNAS)	XP_016883311.1:p.Gln161His
XM_024451872.1:c.-255G>C (GNAS)	XP_024307640.1:n.-255G>C
NM_016592.4:c.483G>C (GNAS)	NP_057676.1:p.Gln161His
NM_016592.5:c.483G>C (GNAS) MANE Plus Clinical	NP_057676.1:p.Gln161His