Canonical Allele Identifier: CA2224102518

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336855A= , CM000678.2:g.56336855A=	GRCh38
NC_000016.9:g.56370767A= , CM000678.1:g.56370767A=	GRCh37
NC_000016.8:g.54928268A=	NCBI36
NG_042800.1:g.150517A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.718A=	ENSP00000262494.7:p.Thr240=
ENST00000262493.12:c.718A= MANE Select	ENSP00000262493.6:p.Thr240=
ENST00000262494.12:c.718A=	ENSP00000262494.7:p.Thr240=
ENST00000562316.6:c.385A=	ENSP00000457238.2:p.Thr129=
ENST00000564727.2:c.22A=	ENSP00000454971.2:p.Thr8=
ENST00000568375.2:c.110A=
ENST00000638185.1:n.933A=
ENST00000638210.1:n.1018A=
ENST00000638705.1:c.718A=	ENSP00000491223.1:p.Thr240=
ENST00000638836.1:n.628A=
ENST00000639055.1:n.1439A=
ENST00000639251.1:n.619A=
ENST00000639268.1:c.353A=
ENST00000639341.1:c.243A=
ENST00000639770.1:c.756A=	ENSP00000491999.1:n.756A=
ENST00000640390.1:n.648A=
ENST00000640469.1:c.82A=	ENSP00000491875.1:p.Thr28=
ENST00000640560.1:n.494A=
ENST00000640893.1:c.*116A=	ENSP00000492677.1:n.*116A=
ENST00000262493.10:c.718A=	ENSP00000262493.6:p.Thr240=
ENST00000262494.11:c.718A=	ENSP00000262494.7:p.Thr240=
ENST00000568375.1:n.110A=
NM_020988.2:c.718A=	NP_066268.1:p.Thr240=
NM_138736.2:c.718A=	NP_620073.2:p.Thr240=
XM_011523003.1:c.592A=	XP_011521305.1:p.Thr198=
XM_011523003.3:c.592A=	XP_011521305.1:p.Thr198=
NM_020988.3:c.718A= MANE Select	NP_066268.1:p.Thr240=
NM_138736.3:c.718A=	NP_620073.2:p.Thr240=