Canonical Allele Identifier: CA495573511

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56368722C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334810C>G , CM000678.2:g.56334810C>G	GRCh38
NC_000016.9:g.56368722C>G , CM000678.1:g.56368722C>G	GRCh37
NC_000016.8:g.54926223C>G	NCBI36
NG_042800.1:g.148472C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.546C>G	ENSP00000262494.7:p.Thr182=
ENST00000262493.12:c.546C>G MANE Select	ENSP00000262493.6:p.Thr182=
ENST00000262494.12:c.546C>G	ENSP00000262494.7:p.Thr182=
ENST00000562316.6:c.213C>G	ENSP00000457238.2:p.Thr71=
ENST00000638185.1:n.761C>G
ENST00000638210.1:n.846C>G
ENST00000638705.1:c.546C>G	ENSP00000491223.1:p.Thr182=
ENST00000638836.1:n.456C>G
ENST00000639055.1:n.1267C>G
ENST00000639251.1:n.447C>G
ENST00000639268.1:c.229-1921C>G
ENST00000639341.1:c.71C>G
ENST00000639770.1:c.584C>G	ENSP00000491999.1:n.584C>G
ENST00000640390.1:n.476C>G
ENST00000640893.1:c.385C>G	ENSP00000492677.1:p.His129Asp
ENST00000262493.10:c.546C>G	ENSP00000262493.6:p.Thr182=
ENST00000262494.11:c.546C>G	ENSP00000262494.7:p.Thr182=
ENST00000562316.5:c.285C>G	ENSP00000457238.1:p.Thr95=
NM_020988.2:c.546C>G	NP_066268.1:p.Thr182=
NM_138736.2:c.546C>G	NP_620073.2:p.Thr182=
XM_011523003.1:c.420C>G	XP_011521305.1:p.Thr140=
XM_011523003.3:c.420C>G	XP_011521305.1:p.Thr140=
NM_020988.3:c.546C>G MANE Select	NP_066268.1:p.Thr182=
NM_138736.3:c.546C>G	NP_620073.2:p.Thr182=