Canonical Allele Identifier: CA2224108762

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351516A= , CM000678.2:g.56351516A=	GRCh38
NC_000016.9:g.56385428A= , CM000678.1:g.56385428A=	GRCh37
NC_000016.8:g.54942929A=	NCBI36
NG_042800.1:g.165178A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.856A= MANE Select	ENSP00000262493.6:p.Ile286=
ENST00000562316.6:c.523A=	ENSP00000457238.2:p.Ile175=
ENST00000564727.2:c.160A=	ENSP00000454971.2:p.Ile54=
ENST00000568375.2:c.116-3350A=
ENST00000638185.1:n.1071A=
ENST00000638210.1:n.1156A=
ENST00000638705.1:c.856A=	ENSP00000491223.1:p.Ile286=
ENST00000638836.1:n.766A=
ENST00000639055.1:n.1577A=
ENST00000639251.1:n.757A=
ENST00000639268.1:c.491A=
ENST00000639341.1:c.381A=
ENST00000639770.1:c.894A=	ENSP00000491999.1:n.894A=
ENST00000640390.1:n.786A=
ENST00000640469.1:c.220A=	ENSP00000491875.1:p.Ile74=
ENST00000640560.1:n.632A=
ENST00000640893.1:c.*254A=	ENSP00000492677.1:n.*254A=
ENST00000262493.10:c.856A=	ENSP00000262493.6:p.Ile286=
ENST00000564727.1:c.76A=	ENSP00000454971.1:p.Ile26=
ENST00000568375.1:n.116-3350A=
NM_020988.2:c.856A=	NP_066268.1:p.Ile286=
XM_011523003.1:c.730A=	XP_011521305.1:p.Ile244=
XM_011523003.3:c.730A=	XP_011521305.1:p.Ile244=
NM_020988.3:c.856A= MANE Select	NP_066268.1:p.Ile286=