Canonical Allele Identifier: CA2224110132

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354971A= , CM000678.2:g.56354971A=	GRCh38
NC_000016.9:g.56388883A= , CM000678.1:g.56388883A=	GRCh37
NC_000016.8:g.54946384A=	NCBI36
NG_042800.1:g.168633A=

Transcript Alleles

HGVS	Amino-acid Change
NM_020988.3:c.983A= MANE Select	NP_066268.1:p.Asp328=
ENST00000262493.12:c.983A= MANE Select	ENSP00000262493.6:p.Asp328=
NM_020988.2:c.983A=	NP_066268.1:p.Asp328=
ENST00000262493.10:c.983A=	ENSP00000262493.6:p.Asp328=
ENST00000562316.6:c.545-1132A=	ENSP00000457238.2:n.545-1132A=
ENST00000564727.1:c.203A=	ENSP00000454971.1:p.Asp68=
ENST00000564727.2:c.287A=	ENSP00000454971.2:p.Asp96=
ENST00000568375.1:n.221A=
ENST00000568375.2:c.221A=
ENST00000638210.1:n.1283A=
ENST00000638705.1:c.983A=	ENSP00000491223.1:p.Asp328=
ENST00000638836.1:n.893A=
ENST00000639251.1:n.884A=
ENST00000639268.1:c.618A=
ENST00000639341.1:c.508A=
ENST00000639770.1:c.1021A=	ENSP00000491999.1:n.1021A=
ENST00000640390.1:n.913A=
ENST00000640469.1:c.347A=	ENSP00000491875.1:p.Asp116=
ENST00000640560.1:n.759A=
ENST00000640893.1:c.*381A=	ENSP00000492677.1:n.*381A=
XM_011523003.1:c.857A=	XP_011521305.1:p.Asp286=
XM_011523003.3:c.857A=	XP_011521305.1:p.Asp286=