Canonical Allele Identifier: CA2224108763

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351518C= , CM000678.2:g.56351518C=	GRCh38
NC_000016.9:g.56385430C= , CM000678.1:g.56385430C=	GRCh37
NC_000016.8:g.54942931C=	NCBI36
NG_042800.1:g.165180C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.858C= MANE Select	ENSP00000262493.6:p.Ile286=
ENST00000562316.6:c.525C=	ENSP00000457238.2:p.Ile175=
ENST00000564727.2:c.162C=	ENSP00000454971.2:p.Ile54=
ENST00000568375.2:c.116-3348C=
ENST00000638185.1:n.1073C=
ENST00000638210.1:n.1158C=
ENST00000638705.1:c.858C=	ENSP00000491223.1:p.Ile286=
ENST00000638836.1:n.768C=
ENST00000639055.1:n.1579C=
ENST00000639251.1:n.759C=
ENST00000639268.1:c.493C=
ENST00000639341.1:c.383C=
ENST00000639770.1:c.896C=	ENSP00000491999.1:n.896C=
ENST00000640390.1:n.788C=
ENST00000640469.1:c.222C=	ENSP00000491875.1:p.Ile74=
ENST00000640560.1:n.634C=
ENST00000640893.1:c.*256C=	ENSP00000492677.1:n.*256C=
ENST00000262493.10:c.858C=	ENSP00000262493.6:p.Ile286=
ENST00000564727.1:c.78C=	ENSP00000454971.1:p.Ile26=
ENST00000568375.1:n.116-3348C=
NM_020988.2:c.858C=	NP_066268.1:p.Ile286=
XM_011523003.1:c.732C=	XP_011521305.1:p.Ile244=
XM_011523003.3:c.732C=	XP_011521305.1:p.Ile244=
NM_020988.3:c.858C= MANE Select	NP_066268.1:p.Ile286=