Canonical Allele Identifier: CA2224102484

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336732C= , CM000678.2:g.56336732C=	GRCh38
NC_000016.9:g.56370644C= , CM000678.1:g.56370644C=	GRCh37
NC_000016.8:g.54928145C=	NCBI36
NG_042800.1:g.150394C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.595C=	ENSP00000262494.7:p.Leu199=
ENST00000262493.12:c.595C= MANE Select	ENSP00000262493.6:p.Leu199=
ENST00000262494.12:c.595C=	ENSP00000262494.7:p.Leu199=
ENST00000562316.6:c.262C=	ENSP00000457238.2:p.Leu88=
ENST00000638185.1:n.810C=
ENST00000638210.1:n.895C=
ENST00000638705.1:c.595C=	ENSP00000491223.1:p.Leu199=
ENST00000638836.1:n.505C=
ENST00000639055.1:n.1316C=
ENST00000639251.1:n.496C=
ENST00000639268.1:c.230C=
ENST00000639341.1:c.120C=
ENST00000639770.1:c.633C=	ENSP00000491999.1:n.633C=
ENST00000640390.1:n.525C=
ENST00000640560.1:n.371C=
ENST00000640893.1:c.434C=	ENSP00000492677.1:p.Ala145=
ENST00000262493.10:c.595C=	ENSP00000262493.6:p.Leu199=
ENST00000262494.11:c.595C=	ENSP00000262494.7:p.Leu199=
NM_020988.2:c.595C=	NP_066268.1:p.Leu199=
NM_138736.2:c.595C=	NP_620073.2:p.Leu199=
XM_011523003.1:c.469C=	XP_011521305.1:p.Leu157=
XM_011523003.3:c.469C=	XP_011521305.1:p.Leu157=
NM_020988.3:c.595C= MANE Select	NP_066268.1:p.Leu199=
NM_138736.3:c.595C=	NP_620073.2:p.Leu199=