Canonical Allele Identifier: CA2224102507

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336817C= , CM000678.2:g.56336817C=	GRCh38
NC_000016.9:g.56370729C= , CM000678.1:g.56370729C=	GRCh37
NC_000016.8:g.54928230C=	NCBI36
NG_042800.1:g.150479C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.680C=	ENSP00000262494.7:p.Ala227=
ENST00000262493.12:c.680C= MANE Select	ENSP00000262493.6:p.Ala227=
ENST00000262494.12:c.680C=	ENSP00000262494.7:p.Ala227=
ENST00000562316.6:c.347C=	ENSP00000457238.2:p.Ala116=
ENST00000568375.2:c.72C=
ENST00000638185.1:n.895C=
ENST00000638210.1:n.980C=
ENST00000638705.1:c.680C=	ENSP00000491223.1:p.Ala227=
ENST00000638836.1:n.590C=
ENST00000639055.1:n.1401C=
ENST00000639251.1:n.581C=
ENST00000639268.1:c.315C=
ENST00000639341.1:c.205C=
ENST00000639770.1:c.718C=	ENSP00000491999.1:n.718C=
ENST00000640390.1:n.610C=
ENST00000640469.1:c.44C=	ENSP00000491875.1:p.Ala15=
ENST00000640560.1:n.456C=
ENST00000640893.1:c.*78C=	ENSP00000492677.1:n.*78C=
ENST00000262493.10:c.680C=	ENSP00000262493.6:p.Ala227=
ENST00000262494.11:c.680C=	ENSP00000262494.7:p.Ala227=
ENST00000568375.1:n.72C=
NM_020988.2:c.680C=	NP_066268.1:p.Ala227=
NM_138736.2:c.680C=	NP_620073.2:p.Ala227=
XM_011523003.1:c.554C=	XP_011521305.1:p.Ala185=
XM_011523003.3:c.554C=	XP_011521305.1:p.Ala185=
NM_020988.3:c.680C= MANE Select	NP_066268.1:p.Ala227=
NM_138736.3:c.680C=	NP_620073.2:p.Ala227=