Canonical Allele Identifier: CA2224102485

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336738G= , CM000678.2:g.56336738G=	GRCh38
NC_000016.9:g.56370650G= , CM000678.1:g.56370650G=	GRCh37
NC_000016.8:g.54928151G=	NCBI36
NG_042800.1:g.150400G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.601G=	ENSP00000262494.7:p.Asp201=
ENST00000262493.12:c.601G= MANE Select	ENSP00000262493.6:p.Asp201=
ENST00000262494.12:c.601G=	ENSP00000262494.7:p.Asp201=
ENST00000562316.6:c.268G=	ENSP00000457238.2:p.Asp90=
ENST00000638185.1:n.816G=
ENST00000638210.1:n.901G=
ENST00000638705.1:c.601G=	ENSP00000491223.1:p.Asp201=
ENST00000638836.1:n.511G=
ENST00000639055.1:n.1322G=
ENST00000639251.1:n.502G=
ENST00000639268.1:c.236G=
ENST00000639341.1:c.126G=
ENST00000639770.1:c.639G=	ENSP00000491999.1:n.639G=
ENST00000640390.1:n.531G=
ENST00000640560.1:n.377G=
ENST00000640893.1:c.440G=	ENSP00000492677.1:p.Ter147=
ENST00000262493.10:c.601G=	ENSP00000262493.6:p.Asp201=
ENST00000262494.11:c.601G=	ENSP00000262494.7:p.Asp201=
NM_020988.2:c.601G=	NP_066268.1:p.Asp201=
NM_138736.2:c.601G=	NP_620073.2:p.Asp201=
XM_011523003.1:c.475G=	XP_011521305.1:p.Asp159=
XM_011523003.3:c.475G=	XP_011521305.1:p.Asp159=
NM_020988.3:c.601G= MANE Select	NP_066268.1:p.Asp201=
NM_138736.3:c.601G=	NP_620073.2:p.Asp201=