Canonical Allele Identifier: CA2224101464

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334758C= , CM000678.2:g.56334758C=	GRCh38
NC_000016.9:g.56368670C= , CM000678.1:g.56368670C=	GRCh37
NC_000016.8:g.54926171C=	NCBI36
NG_042800.1:g.148420C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.494C=	ENSP00000262494.7:p.Ala165=
ENST00000262493.12:c.494C= MANE Select	ENSP00000262493.6:p.Ala165=
ENST00000262494.12:c.494C=	ENSP00000262494.7:p.Ala165=
ENST00000562316.6:c.161C=	ENSP00000457238.2:p.Ala54=
ENST00000638185.1:n.709C=
ENST00000638210.1:n.794C=
ENST00000638705.1:c.494C=	ENSP00000491223.1:p.Ala165=
ENST00000638836.1:n.404C=
ENST00000639055.1:n.1215C=
ENST00000639251.1:n.395C=
ENST00000639268.1:c.229-1973C=
ENST00000639341.1:c.19C=
ENST00000639770.1:c.532C=	ENSP00000491999.1:n.532C=
ENST00000640390.1:n.424C=
ENST00000640893.1:c.333C=	ENSP00000492677.1:p.Gly111=
ENST00000262493.10:c.494C=	ENSP00000262493.6:p.Ala165=
ENST00000262494.11:c.494C=	ENSP00000262494.7:p.Ala165=
ENST00000562316.5:c.233C=	ENSP00000457238.1:p.Ala78=
ENST00000563440.1:c.233C=	ENSP00000455774.1:p.Ala78=
ENST00000565363.5:c.368C=	ENSP00000454728.1:p.Ala123=
NM_020988.2:c.494C=	NP_066268.1:p.Ala165=
NM_138736.2:c.494C=	NP_620073.2:p.Ala165=
XM_011523003.1:c.368C=	XP_011521305.1:p.Ala123=
XM_011523003.3:c.368C=	XP_011521305.1:p.Ala123=
NM_020988.3:c.494C= MANE Select	NP_066268.1:p.Ala165=
NM_138736.3:c.494C=	NP_620073.2:p.Ala165=