Canonical Allele Identifier: CA2224110147

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56355025A= , CM000678.2:g.56355025A=	GRCh38
NC_000016.9:g.56388937A= , CM000678.1:g.56388937A=	GRCh37
NC_000016.8:g.54946438A=	NCBI36
NG_042800.1:g.168687A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.1037A= MANE Select	ENSP00000262493.6:p.Asn346=
ENST00000562316.6:c.545-1078A=	ENSP00000457238.2:n.545-1078A=
ENST00000564727.2:c.303+38A=	ENSP00000454971.2:n.303+38A=
ENST00000568375.2:c.275A=
ENST00000638210.1:n.1337A=
ENST00000638705.1:c.1037A=	ENSP00000491223.1:p.Asn346=
ENST00000638836.1:n.947A=
ENST00000639251.1:n.938A=
ENST00000639268.1:c.672A=
ENST00000639341.1:c.562A=
ENST00000639770.1:c.1075A=	ENSP00000491999.1:n.1075A=
ENST00000640390.1:n.967A=
ENST00000640469.1:c.401A=	ENSP00000491875.1:p.Asn134=
ENST00000640560.1:n.813A=
ENST00000640893.1:c.*435A=	ENSP00000492677.1:n.*435A=
ENST00000262493.10:c.1037A=	ENSP00000262493.6:p.Asn346=
ENST00000564727.1:c.257A=	ENSP00000454971.1:p.Asn86=
ENST00000568375.1:n.275A=
NM_020988.2:c.1037A=	NP_066268.1:p.Asn346=
XM_011523003.1:c.911A=	XP_011521305.1:p.Asn304=
XM_011523003.3:c.911A=	XP_011521305.1:p.Asn304=
NM_020988.3:c.1037A= MANE Select	NP_066268.1:p.Asn346=