Canonical Allele Identifier: CA2224110148

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56355037G= , CM000678.2:g.56355037G=	GRCh38
NC_000016.9:g.56388949G= , CM000678.1:g.56388949G=	GRCh37
NC_000016.8:g.54946450G=	NCBI36
NG_042800.1:g.168699G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.1049G= MANE Select	ENSP00000262493.6:p.Gly350=
ENST00000562316.6:c.545-1066G=	ENSP00000457238.2:n.545-1066G=
ENST00000564727.2:c.303+50G=	ENSP00000454971.2:n.303+50G=
ENST00000568375.2:c.287G=
ENST00000638210.1:n.1349G=
ENST00000638705.1:c.1049G=	ENSP00000491223.1:p.Gly350=
ENST00000638836.1:n.959G=
ENST00000639251.1:n.950G=
ENST00000639268.1:c.684G=
ENST00000639341.1:c.574G=
ENST00000639770.1:c.1087G=	ENSP00000491999.1:n.1087G=
ENST00000640390.1:n.979G=
ENST00000640469.1:c.413G=	ENSP00000491875.1:p.Gly138=
ENST00000640560.1:n.825G=
ENST00000640893.1:c.*447G=	ENSP00000492677.1:n.*447G=
ENST00000262493.10:c.1049G=	ENSP00000262493.6:p.Gly350=
ENST00000564727.1:c.269G=	ENSP00000454971.1:p.Gly90=
ENST00000568375.1:n.287G=
NM_020988.2:c.1049G=	NP_066268.1:p.Gly350=
XM_011523003.1:c.923G=	XP_011521305.1:p.Gly308=
XM_011523003.3:c.923G=	XP_011521305.1:p.Gly308=
NM_020988.3:c.1049G= MANE Select	NP_066268.1:p.Gly350=