Canonical Allele Identifier: CA395952283

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370708C>G (hg19) ; chr16:g.56336796C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336796C>G , CM000678.2:g.56336796C>G	GRCh38
NC_000016.9:g.56370708C>G , CM000678.1:g.56370708C>G	GRCh37
NC_000016.8:g.54928209C>G	NCBI36
NG_042800.1:g.150458C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.659C>G	ENSP00000262494.7:p.Thr220Arg
ENST00000262493.12:c.659C>G MANE Select	ENSP00000262493.6:p.Thr220Arg
ENST00000262494.12:c.659C>G	ENSP00000262494.7:p.Thr220Arg
ENST00000562316.6:c.326C>G	ENSP00000457238.2:p.Thr109Arg
ENST00000568375.2:c.51C>G
ENST00000638185.1:n.874C>G
ENST00000638210.1:n.959C>G
ENST00000638705.1:c.659C>G	ENSP00000491223.1:p.Thr220Arg
ENST00000638836.1:n.569C>G
ENST00000639055.1:n.1380C>G
ENST00000639251.1:n.560C>G
ENST00000639268.1:c.294C>G
ENST00000639341.1:c.184C>G
ENST00000639770.1:c.697C>G	ENSP00000491999.1:n.697C>G
ENST00000640390.1:n.589C>G
ENST00000640469.1:c.23C>G	ENSP00000491875.1:p.Thr8Arg
ENST00000640560.1:n.435C>G
ENST00000640893.1:c.*57C>G	ENSP00000492677.1:n.*57C>G
ENST00000262493.10:c.659C>G	ENSP00000262493.6:p.Thr220Arg
ENST00000262494.11:c.659C>G	ENSP00000262494.7:p.Thr220Arg
ENST00000568375.1:n.51C>G
NM_020988.2:c.659C>G	NP_066268.1:p.Thr220Arg
NM_138736.2:c.659C>G	NP_620073.2:p.Thr220Arg
XM_011523003.1:c.533C>G	XP_011521305.1:p.Thr178Arg
XM_011523003.3:c.533C>G	XP_011521305.1:p.Thr178Arg
NM_020988.3:c.659C>G MANE Select	NP_066268.1:p.Thr220Arg
NM_138736.3:c.659C>G	NP_620073.2:p.Thr220Arg