Canonical Allele Identifier: CA2224110157

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56355062C= , CM000678.2:g.56355062C=	GRCh38
NC_000016.9:g.56388974C= , CM000678.1:g.56388974C=	GRCh37
NC_000016.8:g.54946475C=	NCBI36
NG_042800.1:g.168724C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.*9C= MANE Select	ENSP00000262493.6:n.*9C=
ENST00000562316.6:c.545-1041C=	ENSP00000457238.2:n.545-1041C=
ENST00000564727.2:c.303+75C=	ENSP00000454971.2:n.303+75C=
ENST00000568375.2:c.312C=
ENST00000638210.1:n.1374C=
ENST00000638705.1:c.*9C=	ENSP00000491223.1:n.*9C=
ENST00000638836.1:n.984C=
ENST00000639251.1:n.975C=
ENST00000639268.1:c.709C=
ENST00000639341.1:c.599C=
ENST00000639770.1:c.1112C=	ENSP00000491999.1:n.1112C=
ENST00000640390.1:n.1004C=
ENST00000640469.1:c.438C=	ENSP00000491875.1:n.438C=
ENST00000640560.1:n.850C=
ENST00000640893.1:c.*472C=	ENSP00000492677.1:n.*472C=
ENST00000262493.10:c.*9C=	ENSP00000262493.6:n.*9C=
ENST00000564727.1:c.294C=	ENSP00000454971.1:n.294C=
ENST00000568375.1:n.312C=
NM_020988.2:c.*9C=	NP_066268.1:n.*9C=
XM_011523003.1:c.*9C=	XP_011521305.1:n.*9C=
XM_011523003.3:c.*9C=	XP_011521305.1:n.*9C=
NM_020988.3:c.*9C= MANE Select	NP_066268.1:n.*9C=