Canonical Allele Identifier: CA2224110166

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56355073A= , CM000678.2:g.56355073A=	GRCh38
NC_000016.9:g.56388985A= , CM000678.1:g.56388985A=	GRCh37
NC_000016.8:g.54946486A=	NCBI36
NG_042800.1:g.168735A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.*20A= MANE Select	ENSP00000262493.6:n.*20A=
ENST00000562316.6:c.545-1030A=	ENSP00000457238.2:n.545-1030A=
ENST00000564727.2:c.303+86A=	ENSP00000454971.2:n.303+86A=
ENST00000568375.2:c.323A=
ENST00000638210.1:n.1385A=
ENST00000638705.1:c.*20A=	ENSP00000491223.1:n.*20A=
ENST00000638836.1:n.995A=
ENST00000639251.1:n.986A=
ENST00000639268.1:c.720A=
ENST00000639341.1:c.610A=
ENST00000639770.1:c.1123A=	ENSP00000491999.1:n.1123A=
ENST00000640390.1:n.1015A=
ENST00000640469.1:c.449A=	ENSP00000491875.1:n.449A=
ENST00000640560.1:n.861A=
ENST00000640893.1:c.*483A=	ENSP00000492677.1:n.*483A=
ENST00000262493.10:c.*20A=	ENSP00000262493.6:n.*20A=
ENST00000564727.1:c.305A=	ENSP00000454971.1:n.305A=
ENST00000568375.1:n.323A=
NM_020988.2:c.*20A=	NP_066268.1:n.*20A=
XM_011523003.1:c.*20A=	XP_011521305.1:n.*20A=
XM_011523003.3:c.*20A=	XP_011521305.1:n.*20A=
NM_020988.3:c.*20A= MANE Select	NP_066268.1:n.*20A=