Canonical Allele Identifier: CA2224108757

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351499A= , CM000678.2:g.56351499A=	GRCh38
NC_000016.9:g.56385411A= , CM000678.1:g.56385411A=	GRCh37
NC_000016.8:g.54942912A=	NCBI36
NG_042800.1:g.165161A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.839A= MANE Select	ENSP00000262493.6:p.Lys280=
ENST00000562316.6:c.506A=	ENSP00000457238.2:p.Lys169=
ENST00000564727.2:c.143A=	ENSP00000454971.2:p.Lys48=
ENST00000568375.2:c.116-3367A=
ENST00000638185.1:n.1054A=
ENST00000638210.1:n.1139A=
ENST00000638705.1:c.839A=	ENSP00000491223.1:p.Lys280=
ENST00000638836.1:n.749A=
ENST00000639055.1:n.1560A=
ENST00000639251.1:n.740A=
ENST00000639268.1:c.474A=
ENST00000639341.1:c.364A=
ENST00000639770.1:c.877A=	ENSP00000491999.1:n.877A=
ENST00000640390.1:n.769A=
ENST00000640469.1:c.203A=	ENSP00000491875.1:p.Lys68=
ENST00000640560.1:n.615A=
ENST00000640893.1:c.*237A=	ENSP00000492677.1:n.*237A=
ENST00000262493.10:c.839A=	ENSP00000262493.6:p.Lys280=
ENST00000564727.1:c.59A=	ENSP00000454971.1:p.Lys20=
ENST00000568375.1:n.116-3367A=
NM_020988.2:c.839A=	NP_066268.1:p.Lys280=
XM_011523003.1:c.713A=	XP_011521305.1:p.Lys238=
XM_011523003.3:c.713A=	XP_011521305.1:p.Lys238=
NM_020988.3:c.839A= MANE Select	NP_066268.1:p.Lys280=