Canonical Allele Identifier: CA2224108751

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351478A= , CM000678.2:g.56351478A=	GRCh38
NC_000016.9:g.56385390A= , CM000678.1:g.56385390A=	GRCh37
NC_000016.8:g.54942891A=	NCBI36
NG_042800.1:g.165140A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.818A= MANE Select	ENSP00000262493.6:p.Asp273=
ENST00000562316.6:c.485A=	ENSP00000457238.2:p.Asp162=
ENST00000564727.2:c.122A=	ENSP00000454971.2:p.Asp41=
ENST00000568375.2:c.116-3388A=
ENST00000638185.1:n.1033A=
ENST00000638210.1:n.1118A=
ENST00000638705.1:c.818A=	ENSP00000491223.1:p.Asp273=
ENST00000638836.1:n.728A=
ENST00000639055.1:n.1539A=
ENST00000639251.1:n.719A=
ENST00000639268.1:c.453A=
ENST00000639341.1:c.343A=
ENST00000639770.1:c.856A=	ENSP00000491999.1:n.856A=
ENST00000640390.1:n.748A=
ENST00000640469.1:c.182A=	ENSP00000491875.1:p.Asp61=
ENST00000640560.1:n.594A=
ENST00000640893.1:c.*216A=	ENSP00000492677.1:n.*216A=
ENST00000262493.10:c.818A=	ENSP00000262493.6:p.Asp273=
ENST00000564727.1:c.38A=	ENSP00000454971.1:p.Asp13=
ENST00000568375.1:n.116-3388A=
NM_020988.2:c.818A=	NP_066268.1:p.Asp273=
XM_011523003.1:c.692A=	XP_011521305.1:p.Asp231=
XM_011523003.3:c.692A=	XP_011521305.1:p.Asp231=
NM_020988.3:c.818A= MANE Select	NP_066268.1:p.Asp273=