Canonical Allele Identifier: CA495573502

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56368707A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334795A>G , CM000678.2:g.56334795A>G	GRCh38
NC_000016.9:g.56368707A>G , CM000678.1:g.56368707A>G	GRCh37
NC_000016.8:g.54926208A>G	NCBI36
NG_042800.1:g.148457A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.531A>G	ENSP00000262494.7:p.Arg177=
ENST00000262493.12:c.531A>G MANE Select	ENSP00000262493.6:p.Arg177=
ENST00000262494.12:c.531A>G	ENSP00000262494.7:p.Arg177=
ENST00000562316.6:c.198A>G	ENSP00000457238.2:p.Arg66=
ENST00000638185.1:n.746A>G
ENST00000638210.1:n.831A>G
ENST00000638705.1:c.531A>G	ENSP00000491223.1:p.Arg177=
ENST00000638836.1:n.441A>G
ENST00000639055.1:n.1252A>G
ENST00000639251.1:n.432A>G
ENST00000639268.1:c.229-1936A>G
ENST00000639341.1:c.56A>G
ENST00000639770.1:c.569A>G	ENSP00000491999.1:n.569A>G
ENST00000640390.1:n.461A>G
ENST00000640893.1:c.370A>G	ENSP00000492677.1:p.Asn124Asp
ENST00000262493.10:c.531A>G	ENSP00000262493.6:p.Arg177=
ENST00000262494.11:c.531A>G	ENSP00000262494.7:p.Arg177=
ENST00000562316.5:c.270A>G	ENSP00000457238.1:p.Arg90=
NM_020988.2:c.531A>G	NP_066268.1:p.Arg177=
NM_138736.2:c.531A>G	NP_620073.2:p.Arg177=
XM_011523003.1:c.405A>G	XP_011521305.1:p.Arg135=
XM_011523003.3:c.405A>G	XP_011521305.1:p.Arg135=
NM_020988.3:c.531A>G MANE Select	NP_066268.1:p.Arg177=
NM_138736.3:c.531A>G	NP_620073.2:p.Arg177=