Canonical Allele Identifier: CA409453432

Gene: GNAS GNAS-AS1

Linked Data

• MyVariant Identifiers: chr20:g.57415862C>A (hg19) ; chr20:g.58840807C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58840807C>A , CM000682.2:g.58840807C>A	GRCh38
NC_000020.10:g.57415862C>A , CM000682.1:g.57415862C>A	GRCh37
NC_000020.9:g.56849257C>A	NCBI36
NG_016194.1:g.6068C>A
NG_021433.1:g.15097G>T
NG_016194.2:g.6068C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419558.7:c.701C>A (GNAS)	ENSP00000416234.2:p.Pro234His
ENST00000453292.7:c.701C>A (GNAS)	ENSP00000392000.2:p.Pro234His
ENST00000419558.6:c.701C>A (GNAS)	ENSP00000416234.2:p.Pro234His
ENST00000453292.6:c.701C>A (GNAS)	ENSP00000392000.2:p.Pro234His
ENST00000657090.1:c.-39+867C>A (GNAS)	ENSP00000499380.1:n.-39+867C>A
ENST00000667293.1:c.-27-43C>A (GNAS)	ENSP00000499293.1:n.-27-43C>A
ENST00000313949.11:c.701C>A (GNAS)	ENSP00000323571.7:p.Pro234His
ENST00000371075.7:c.701C>A (GNAS) MANE Plus Clinical	ENSP00000360115.3:p.Pro234His
ENST00000371098.6:c.701C>A (GNAS)	ENSP00000360139.2:p.Pro234His
ENST00000419558.5:c.304C>A (GNAS)
ENST00000453292.5:c.464C>A (GNAS)	ENSP00000392000.1:p.Pro155His
NM_016592.2:c.701C>A (GNAS)	NP_057676.1:p.Pro234His
NM_016592.3:c.701C>A (GNAS)	NP_057676.1:p.Pro234His
NR_002785.2:n.819+1130G>T (GNAS-AS1)
XM_017027815.1:c.-37C>A (GNAS)	XP_016883304.1:n.-37C>A
XM_017027821.1:c.701C>A (GNAS)	XP_016883310.1:p.Pro234His
XM_017027822.1:c.701C>A (GNAS)	XP_016883311.1:p.Pro234His
XM_024451872.1:c.-37C>A (GNAS)	XP_024307640.1:n.-37C>A
NM_016592.4:c.701C>A (GNAS)	NP_057676.1:p.Pro234His
NM_016592.5:c.701C>A (GNAS) MANE Plus Clinical	NP_057676.1:p.Pro234His