Canonical Allele Identifier: CA395952370

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370747A>G (hg19) ; chr16:g.56336835A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336835A>G , CM000678.2:g.56336835A>G	GRCh38
NC_000016.9:g.56370747A>G , CM000678.1:g.56370747A>G	GRCh37
NC_000016.8:g.54928248A>G	NCBI36
NG_042800.1:g.150497A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.698A>G	ENSP00000262494.7:p.Gln233Arg
ENST00000262493.12:c.698A>G MANE Select	ENSP00000262493.6:p.Gln233Arg
ENST00000262494.12:c.698A>G	ENSP00000262494.7:p.Gln233Arg
ENST00000562316.6:c.365A>G	ENSP00000457238.2:p.Gln122Arg
ENST00000564727.2:c.2A>G	ENSP00000454971.2:p.Gln1Arg
ENST00000568375.2:c.90A>G
ENST00000638185.1:n.913A>G
ENST00000638210.1:n.998A>G
ENST00000638705.1:c.698A>G	ENSP00000491223.1:p.Gln233Arg
ENST00000638836.1:n.608A>G
ENST00000639055.1:n.1419A>G
ENST00000639251.1:n.599A>G
ENST00000639268.1:c.333A>G
ENST00000639341.1:c.223A>G
ENST00000639770.1:c.736A>G	ENSP00000491999.1:n.736A>G
ENST00000640390.1:n.628A>G
ENST00000640469.1:c.62A>G	ENSP00000491875.1:p.Gln21Arg
ENST00000640560.1:n.474A>G
ENST00000640893.1:c.*96A>G	ENSP00000492677.1:n.*96A>G
ENST00000262493.10:c.698A>G	ENSP00000262493.6:p.Gln233Arg
ENST00000262494.11:c.698A>G	ENSP00000262494.7:p.Gln233Arg
ENST00000568375.1:n.90A>G
NM_020988.2:c.698A>G	NP_066268.1:p.Gln233Arg
NM_138736.2:c.698A>G	NP_620073.2:p.Gln233Arg
XM_011523003.1:c.572A>G	XP_011521305.1:p.Gln191Arg
XM_011523003.3:c.572A>G	XP_011521305.1:p.Gln191Arg
NM_020988.3:c.698A>G MANE Select	NP_066268.1:p.Gln233Arg
NM_138736.3:c.698A>G	NP_620073.2:p.Gln233Arg