Canonical Allele Identifier: CA2224110109

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354868C= , CM000678.2:g.56354868C=	GRCh38
NC_000016.9:g.56388780C= , CM000678.1:g.56388780C=	GRCh37
NC_000016.8:g.54946281C=	NCBI36
NG_042800.1:g.168530C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.880C= MANE Select	ENSP00000262493.6:p.Pro294=
ENST00000562316.6:c.545-1235C=	ENSP00000457238.2:n.545-1235C=
ENST00000564727.2:c.184C=	ENSP00000454971.2:p.Pro62=
ENST00000568375.2:c.118C=
ENST00000638185.1:n.1095C=
ENST00000638210.1:n.1180C=
ENST00000638705.1:c.880C=	ENSP00000491223.1:p.Pro294=
ENST00000638836.1:n.790C=
ENST00000639055.1:n.1601C=
ENST00000639251.1:n.781C=
ENST00000639268.1:c.515C=
ENST00000639341.1:c.405C=
ENST00000639770.1:c.918C=	ENSP00000491999.1:n.918C=
ENST00000640390.1:n.810C=
ENST00000640469.1:c.244C=	ENSP00000491875.1:p.Pro82=
ENST00000640560.1:n.656C=
ENST00000640893.1:c.*278C=	ENSP00000492677.1:n.*278C=
ENST00000262493.10:c.880C=	ENSP00000262493.6:p.Pro294=
ENST00000564727.1:c.100C=	ENSP00000454971.1:p.Pro34=
ENST00000568375.1:n.118C=
NM_020988.2:c.880C=	NP_066268.1:p.Pro294=
XM_011523003.1:c.754C=	XP_011521305.1:p.Pro252=
XM_011523003.3:c.754C=	XP_011521305.1:p.Pro252=
NM_020988.3:c.880C= MANE Select	NP_066268.1:p.Pro294=