Canonical Allele Identifier: CA495573594

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370676C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336764C>G , CM000678.2:g.56336764C>G	GRCh38
NC_000016.9:g.56370676C>G , CM000678.1:g.56370676C>G	GRCh37
NC_000016.8:g.54928177C>G	NCBI36
NG_042800.1:g.150426C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.627C>G	ENSP00000262494.7:p.Arg209=
ENST00000262493.12:c.627C>G MANE Select	ENSP00000262493.6:p.Arg209=
ENST00000262494.12:c.627C>G	ENSP00000262494.7:p.Arg209=
ENST00000562316.6:c.294C>G	ENSP00000457238.2:p.Arg98=
ENST00000568375.2:c.19C>G
ENST00000638185.1:n.842C>G
ENST00000638210.1:n.927C>G
ENST00000638705.1:c.627C>G	ENSP00000491223.1:p.Arg209=
ENST00000638836.1:n.537C>G
ENST00000639055.1:n.1348C>G
ENST00000639251.1:n.528C>G
ENST00000639268.1:c.262C>G
ENST00000639341.1:c.152C>G
ENST00000639770.1:c.665C>G	ENSP00000491999.1:n.665C>G
ENST00000640390.1:n.557C>G
ENST00000640560.1:n.403C>G
ENST00000640893.1:c.*25C>G	ENSP00000492677.1:n.*25C>G
ENST00000262493.10:c.627C>G	ENSP00000262493.6:p.Arg209=
ENST00000262494.11:c.627C>G	ENSP00000262494.7:p.Arg209=
ENST00000568375.1:n.19C>G
NM_020988.2:c.627C>G	NP_066268.1:p.Arg209=
NM_138736.2:c.627C>G	NP_620073.2:p.Arg209=
XM_011523003.1:c.501C>G	XP_011521305.1:p.Arg167=
XM_011523003.3:c.501C>G	XP_011521305.1:p.Arg167=
NM_020988.3:c.627C>G MANE Select	NP_066268.1:p.Arg209=
NM_138736.3:c.627C>G	NP_620073.2:p.Arg209=