Canonical Allele Identifier: CA2224108755

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351494G= , CM000678.2:g.56351494G=	GRCh38
NC_000016.9:g.56385406G= , CM000678.1:g.56385406G=	GRCh37
NC_000016.8:g.54942907G=	NCBI36
NG_042800.1:g.165156G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.834G= MANE Select	ENSP00000262493.6:p.Lys278=
ENST00000562316.6:c.501G=	ENSP00000457238.2:p.Lys167=
ENST00000564727.2:c.138G=	ENSP00000454971.2:p.Lys46=
ENST00000568375.2:c.116-3372G=
ENST00000638185.1:n.1049G=
ENST00000638210.1:n.1134G=
ENST00000638705.1:c.834G=	ENSP00000491223.1:p.Lys278=
ENST00000638836.1:n.744G=
ENST00000639055.1:n.1555G=
ENST00000639251.1:n.735G=
ENST00000639268.1:c.469G=
ENST00000639341.1:c.359G=
ENST00000639770.1:c.872G=	ENSP00000491999.1:n.872G=
ENST00000640390.1:n.764G=
ENST00000640469.1:c.198G=	ENSP00000491875.1:p.Lys66=
ENST00000640560.1:n.610G=
ENST00000640893.1:c.*232G=	ENSP00000492677.1:n.*232G=
ENST00000262493.10:c.834G=	ENSP00000262493.6:p.Lys278=
ENST00000564727.1:c.54G=	ENSP00000454971.1:p.Lys18=
ENST00000568375.1:n.116-3372G=
NM_020988.2:c.834G=	NP_066268.1:p.Lys278=
XM_011523003.1:c.708G=	XP_011521305.1:p.Lys236=
XM_011523003.3:c.708G=	XP_011521305.1:p.Lys236=
NM_020988.3:c.834G= MANE Select	NP_066268.1:p.Lys278=