Canonical Allele Identifier: CA2224102493

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336754G= , CM000678.2:g.56336754G=	GRCh38
NC_000016.9:g.56370666G= , CM000678.1:g.56370666G=	GRCh37
NC_000016.8:g.54928167G=	NCBI36
NG_042800.1:g.150416G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.617G=	ENSP00000262494.7:p.Arg206=
ENST00000262493.12:c.617G= MANE Select	ENSP00000262493.6:p.Arg206=
ENST00000262494.12:c.617G=	ENSP00000262494.7:p.Arg206=
ENST00000562316.6:c.284G=	ENSP00000457238.2:p.Arg95=
ENST00000568375.2:c.9G=
ENST00000638185.1:n.832G=
ENST00000638210.1:n.917G=
ENST00000638705.1:c.617G=	ENSP00000491223.1:p.Arg206=
ENST00000638836.1:n.527G=
ENST00000639055.1:n.1338G=
ENST00000639251.1:n.518G=
ENST00000639268.1:c.252G=
ENST00000639341.1:c.142G=
ENST00000639770.1:c.655G=	ENSP00000491999.1:n.655G=
ENST00000640390.1:n.547G=
ENST00000640560.1:n.393G=
ENST00000640893.1:c.*15G=	ENSP00000492677.1:n.*15G=
ENST00000262493.10:c.617G=	ENSP00000262493.6:p.Arg206=
ENST00000262494.11:c.617G=	ENSP00000262494.7:p.Arg206=
ENST00000568375.1:n.9G=
NM_020988.2:c.617G=	NP_066268.1:p.Arg206=
NM_138736.2:c.617G=	NP_620073.2:p.Arg206=
XM_011523003.1:c.491G=	XP_011521305.1:p.Arg164=
XM_011523003.3:c.491G=	XP_011521305.1:p.Arg164=
NM_020988.3:c.617G= MANE Select	NP_066268.1:p.Arg206=
NM_138736.3:c.617G=	NP_620073.2:p.Arg206=