Canonical Allele Identifier: CA2224108748

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351469A= , CM000678.2:g.56351469A=	GRCh38
NC_000016.9:g.56385381A= , CM000678.1:g.56385381A=	GRCh37
NC_000016.8:g.54942882A=	NCBI36
NG_042800.1:g.165131A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.809A= MANE Select	ENSP00000262493.6:p.Asn270=
ENST00000562316.6:c.476A=	ENSP00000457238.2:p.Asn159=
ENST00000564727.2:c.113A=	ENSP00000454971.2:p.Asn38=
ENST00000568375.2:c.116-3397A=
ENST00000638185.1:n.1024A=
ENST00000638210.1:n.1109A=
ENST00000638705.1:c.809A=	ENSP00000491223.1:p.Asn270=
ENST00000638836.1:n.719A=
ENST00000639055.1:n.1530A=
ENST00000639251.1:n.710A=
ENST00000639268.1:c.444A=
ENST00000639341.1:c.334A=
ENST00000639770.1:c.847A=	ENSP00000491999.1:n.847A=
ENST00000640390.1:n.739A=
ENST00000640469.1:c.173A=	ENSP00000491875.1:p.Asn58=
ENST00000640560.1:n.585A=
ENST00000640893.1:c.*207A=	ENSP00000492677.1:n.*207A=
ENST00000262493.10:c.809A=	ENSP00000262493.6:p.Asn270=
ENST00000564727.1:c.29A=	ENSP00000454971.1:p.Asn10=
ENST00000568375.1:n.116-3397A=
NM_020988.2:c.809A=	NP_066268.1:p.Asn270=
XM_011523003.1:c.683A=	XP_011521305.1:p.Asn228=
XM_011523003.3:c.683A=	XP_011521305.1:p.Asn228=
NM_020988.3:c.809A= MANE Select	NP_066268.1:p.Asn270=