Canonical Allele Identifier: CA2224110127

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354935A= , CM000678.2:g.56354935A=	GRCh38
NC_000016.9:g.56388847A= , CM000678.1:g.56388847A=	GRCh37
NC_000016.8:g.54946348A=	NCBI36
NG_042800.1:g.168597A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.947A= MANE Select	ENSP00000262493.6:p.Asn316=
ENST00000562316.6:c.545-1168A=	ENSP00000457238.2:n.545-1168A=
ENST00000564727.2:c.251A=	ENSP00000454971.2:p.Asn84=
ENST00000568375.2:c.185A=
ENST00000638185.1:n.1162A=
ENST00000638210.1:n.1247A=
ENST00000638705.1:c.947A=	ENSP00000491223.1:p.Asn316=
ENST00000638836.1:n.857A=
ENST00000639055.1:n.1668A=
ENST00000639251.1:n.848A=
ENST00000639268.1:c.582A=
ENST00000639341.1:c.472A=
ENST00000639770.1:c.985A=	ENSP00000491999.1:n.985A=
ENST00000640390.1:n.877A=
ENST00000640469.1:c.311A=	ENSP00000491875.1:p.Asn104=
ENST00000640560.1:n.723A=
ENST00000640893.1:c.*345A=	ENSP00000492677.1:n.*345A=
ENST00000262493.10:c.947A=	ENSP00000262493.6:p.Asn316=
ENST00000564727.1:c.167A=	ENSP00000454971.1:p.Asn56=
ENST00000568375.1:n.185A=
NM_020988.2:c.947A=	NP_066268.1:p.Asn316=
XM_011523003.1:c.821A=	XP_011521305.1:p.Asn274=
XM_011523003.3:c.821A=	XP_011521305.1:p.Asn274=
NM_020988.3:c.947A= MANE Select	NP_066268.1:p.Asn316=