Canonical Allele Identifier: CA495573564

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370643G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336731G>A , CM000678.2:g.56336731G>A	GRCh38
NC_000016.9:g.56370643G>A , CM000678.1:g.56370643G>A	GRCh37
NC_000016.8:g.54928144G>A	NCBI36
NG_042800.1:g.150393G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262494.13:c.594G>A	ENSP00000262494.7:p.Arg198=
ENST00000262493.12:c.594G>A MANE Select	ENSP00000262493.6:p.Arg198=
ENST00000262494.12:c.594G>A	ENSP00000262494.7:p.Arg198=
ENST00000562316.6:c.261G>A	ENSP00000457238.2:p.Arg87=
ENST00000638185.1:n.809G>A
ENST00000638210.1:n.894G>A
ENST00000638705.1:c.594G>A	ENSP00000491223.1:p.Arg198=
ENST00000638836.1:n.504G>A
ENST00000639055.1:n.1315G>A
ENST00000639251.1:n.495G>A
ENST00000639268.1:c.229G>A
ENST00000639341.1:c.119G>A
ENST00000639770.1:c.632G>A	ENSP00000491999.1:n.632G>A
ENST00000640390.1:n.524G>A
ENST00000640560.1:n.370G>A
ENST00000640893.1:c.433G>A	ENSP00000492677.1:p.Ala145Thr
ENST00000262493.10:c.594G>A	ENSP00000262493.6:p.Arg198=
ENST00000262494.11:c.594G>A	ENSP00000262494.7:p.Arg198=
NM_020988.2:c.594G>A	NP_066268.1:p.Arg198=
NM_138736.2:c.594G>A	NP_620073.2:p.Arg198=
XM_011523003.1:c.468G>A	XP_011521305.1:p.Arg156=
XM_011523003.3:c.468G>A	XP_011521305.1:p.Arg156=
NM_020988.3:c.594G>A MANE Select	NP_066268.1:p.Arg198=
NM_138736.3:c.594G>A	NP_620073.2:p.Arg198=