Canonical Allele Identifier: CA409451802
Gene: GNAS HGNC NCBI
GNAS-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.58840549T>C , CM000682.2:g.58840549T>C GRCh38
NC_000020.10:g.57415604T>C , CM000682.1:g.57415604T>C GRCh37
NC_000020.9:g.56848999T>C NCBI36
NG_016194.1:g.5810T>C
NG_021433.1:g.15355A>G
NG_016194.2:g.5810T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000419558.7:c.443T>C (GNAS) ENSP00000416234.2:p.Val148Ala
ENST00000453292.7:c.443T>C (GNAS) ENSP00000392000.2:p.Val148Ala
ENST00000419558.6:c.443T>C (GNAS) ENSP00000416234.2:p.Val148Ala
ENST00000453292.6:c.443T>C (GNAS) ENSP00000392000.2:p.Val148Ala
ENST00000657090.1:c.-39+609T>C (GNAS) ENSP00000499380.1:n.-39+609T>C
ENST00000667293.1:c.-27-301T>C (GNAS) ENSP00000499293.1:n.-27-301T>C
ENST00000313949.11:c.443T>C (GNAS) ENSP00000323571.7:p.Val148Ala
ENST00000371075.7:c.443T>C (GNAS) MANE Plus Clinical ENSP00000360115.3:p.Val148Ala
ENST00000371098.6:c.443T>C (GNAS) ENSP00000360139.2:p.Val148Ala
ENST00000419558.5:c.46T>C (GNAS)
ENST00000453292.5:c.206T>C (GNAS) ENSP00000392000.1:p.Val69Ala
NM_016592.2:c.443T>C (GNAS) NP_057676.1:p.Val148Ala
NM_016592.3:c.443T>C (GNAS) NP_057676.1:p.Val148Ala
NR_002785.2:n.819+1388A>G (GNAS-AS1)
XM_017027821.1:c.443T>C (GNAS) XP_016883310.1:p.Val148Ala
XM_017027822.1:c.443T>C (GNAS) XP_016883311.1:p.Val148Ala
XM_024451872.1:c.-295T>C (GNAS) XP_024307640.1:n.-295T>C
NM_016592.4:c.443T>C (GNAS) NP_057676.1:p.Val148Ala
NM_016592.5:c.443T>C (GNAS) MANE Plus Clinical NP_057676.1:p.Val148Ala