Canonical Allele Identifier: CA2224102496

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336763G= , CM000678.2:g.56336763G=	GRCh38
NC_000016.9:g.56370675G= , CM000678.1:g.56370675G=	GRCh37
NC_000016.8:g.54928176G=	NCBI36
NG_042800.1:g.150425G=

Transcript Alleles

HGVS	Amino-acid Change
NM_020988.3:c.626G= MANE Select	NP_066268.1:p.Arg209=
ENST00000262493.12:c.626G= MANE Select	ENSP00000262493.6:p.Arg209=
NM_020988.2:c.626G=	NP_066268.1:p.Arg209=
NM_138736.2:c.626G=	NP_620073.2:p.Arg209=
NM_138736.3:c.626G=	NP_620073.2:p.Arg209=
ENST00000262493.10:c.626G=	ENSP00000262493.6:p.Arg209=
ENST00000262494.11:c.626G=	ENSP00000262494.7:p.Arg209=
ENST00000262494.12:c.626G=	ENSP00000262494.7:p.Arg209=
ENST00000262494.13:c.626G=	ENSP00000262494.7:p.Arg209=
ENST00000562316.6:c.293G=	ENSP00000457238.2:p.Arg98=
ENST00000568375.1:n.18G=
ENST00000568375.2:c.18G=
ENST00000638185.1:n.841G=
ENST00000638210.1:n.926G=
ENST00000638705.1:c.626G=	ENSP00000491223.1:p.Arg209=
ENST00000638836.1:n.536G=
ENST00000639055.1:n.1347G=
ENST00000639251.1:n.527G=
ENST00000639268.1:c.261G=
ENST00000639341.1:c.151G=
ENST00000639770.1:c.664G=	ENSP00000491999.1:n.664G=
ENST00000640390.1:n.556G=
ENST00000640560.1:n.402G=
ENST00000640893.1:c.*24G=	ENSP00000492677.1:n.*24G=
XM_011523003.1:c.500G=	XP_011521305.1:p.Arg167=
XM_011523003.3:c.500G=	XP_011521305.1:p.Arg167=