Canonical Allele Identifier: CA2577436196

Gene: GNAS GNAS-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58840859C>T , CM000682.2:g.58840859C>T	GRCh38
NC_000020.10:g.57415914C>T , CM000682.1:g.57415914C>T	GRCh37
NC_000020.9:g.56849309C>T	NCBI36
NG_016194.1:g.6120C>T
NG_021433.1:g.15045G>A
NG_016194.2:g.6120C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419558.7:c.*15C>T (GNAS)	ENSP00000416234.2:n.*15C>T
ENST00000453292.7:c.753C>T (GNAS)	ENSP00000392000.2:n.753C>T
ENST00000306090.12:c.16C>T (GNAS)	ENSP00000304472.12:p.Gln6Ter
ENST00000419558.6:c.*15C>T (GNAS)	ENSP00000416234.2:n.*15C>T
ENST00000453292.6:c.*15C>T (GNAS)	ENSP00000392000.2:n.*15C>T
ENST00000657090.1:c.-39+919C>T (GNAS)	ENSP00000499380.1:n.-39+919C>T
ENST00000667293.1:c.-18C>T (GNAS)	ENSP00000499293.1:n.-18C>T
ENST00000313949.11:c.*15C>T (GNAS)	ENSP00000323571.7:n.*15C>T
ENST00000371075.7:c.*15C>T (GNAS) MANE Plus Clinical	ENSP00000360115.3:n.*15C>T
ENST00000371098.6:c.*15C>T (GNAS)	ENSP00000360139.2:n.*15C>T
ENST00000419558.5:c.356C>T (GNAS)
ENST00000453292.5:c.516C>T (GNAS)	ENSP00000392000.1:n.516C>T
NM_016592.2:c.*15C>T (GNAS)	NP_057676.1:n.*15C>T
NM_016592.3:c.*15C>T (GNAS)	NP_057676.1:n.*15C>T
NR_002785.2:n.819+1078G>A (GNAS-AS1)
XM_017027815.1:c.16C>T (GNAS)	XP_016883304.1:p.Gln6Ter
XM_017027821.1:c.*15C>T (GNAS)	XP_016883310.1:n.*15C>T
XM_017027822.1:c.*15C>T (GNAS)	XP_016883311.1:n.*15C>T
XM_024451872.1:c.16C>T (GNAS)	XP_024307640.1:p.Gln6Ter
NM_016592.4:c.*15C>T (GNAS)	NP_057676.1:n.*15C>T
NM_016592.5:c.*15C>T (GNAS) MANE Plus Clinical	NP_057676.1:n.*15C>T