Canonical Allele Identifier: CA2224108756

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351496T= , CM000678.2:g.56351496T=	GRCh38
NC_000016.9:g.56385408T= , CM000678.1:g.56385408T=	GRCh37
NC_000016.8:g.54942909T=	NCBI36
NG_042800.1:g.165158T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.836T= MANE Select	ENSP00000262493.6:p.Ile279=
ENST00000562316.6:c.503T=	ENSP00000457238.2:p.Ile168=
ENST00000564727.2:c.140T=	ENSP00000454971.2:p.Ile47=
ENST00000568375.2:c.116-3370T=
ENST00000638185.1:n.1051T=
ENST00000638210.1:n.1136T=
ENST00000638705.1:c.836T=	ENSP00000491223.1:p.Ile279=
ENST00000638836.1:n.746T=
ENST00000639055.1:n.1557T=
ENST00000639251.1:n.737T=
ENST00000639268.1:c.471T=
ENST00000639341.1:c.361T=
ENST00000639770.1:c.874T=	ENSP00000491999.1:n.874T=
ENST00000640390.1:n.766T=
ENST00000640469.1:c.200T=	ENSP00000491875.1:p.Ile67=
ENST00000640560.1:n.612T=
ENST00000640893.1:c.*234T=	ENSP00000492677.1:n.*234T=
ENST00000262493.10:c.836T=	ENSP00000262493.6:p.Ile279=
ENST00000564727.1:c.56T=	ENSP00000454971.1:p.Ile19=
ENST00000568375.1:n.116-3370T=
NM_020988.2:c.836T=	NP_066268.1:p.Ile279=
XM_011523003.1:c.710T=	XP_011521305.1:p.Ile237=
XM_011523003.3:c.710T=	XP_011521305.1:p.Ile237=
NM_020988.3:c.836T= MANE Select	NP_066268.1:p.Ile279=