Canonical Allele Identifier: CA2224102495

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336762C= , CM000678.2:g.56336762C=	GRCh38
NC_000016.9:g.56370674C= , CM000678.1:g.56370674C=	GRCh37
NC_000016.8:g.54928175C=	NCBI36
NG_042800.1:g.150424C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.625C=	ENSP00000262494.7:p.Arg209=
ENST00000262493.12:c.625C= MANE Select	ENSP00000262493.6:p.Arg209=
ENST00000262494.12:c.625C=	ENSP00000262494.7:p.Arg209=
ENST00000562316.6:c.292C=	ENSP00000457238.2:p.Arg98=
ENST00000568375.2:c.17C=
ENST00000638185.1:n.840C=
ENST00000638210.1:n.925C=
ENST00000638705.1:c.625C=	ENSP00000491223.1:p.Arg209=
ENST00000638836.1:n.535C=
ENST00000639055.1:n.1346C=
ENST00000639251.1:n.526C=
ENST00000639268.1:c.260C=
ENST00000639341.1:c.150C=
ENST00000639770.1:c.663C=	ENSP00000491999.1:n.663C=
ENST00000640390.1:n.555C=
ENST00000640560.1:n.401C=
ENST00000640893.1:c.*23C=	ENSP00000492677.1:n.*23C=
ENST00000262493.10:c.625C=	ENSP00000262493.6:p.Arg209=
ENST00000262494.11:c.625C=	ENSP00000262494.7:p.Arg209=
ENST00000568375.1:n.17C=
NM_020988.2:c.625C=	NP_066268.1:p.Arg209=
NM_138736.2:c.625C=	NP_620073.2:p.Arg209=
XM_011523003.1:c.499C=	XP_011521305.1:p.Arg167=
XM_011523003.3:c.499C=	XP_011521305.1:p.Arg167=
NM_020988.3:c.625C= MANE Select	NP_066268.1:p.Arg209=
NM_138736.3:c.625C=	NP_620073.2:p.Arg209=