Canonical Allele Identifier: CA2633321926

Gene: GNAO1

Linked Data

• gnomAD v4: 16-56351536-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351536A>G , CM000678.2:g.56351536A>G	GRCh38
NC_000016.9:g.56385448A>G , CM000678.1:g.56385448A>G	GRCh37
NC_000016.8:g.54942949A>G	NCBI36
NG_042800.1:g.165198A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262493.12:c.876A>G MANE Select	ENSP00000262493.6:p.Thr292=
ENST00000562316.6:c.543A>G	ENSP00000457238.2:p.Thr181=
ENST00000564727.2:c.180A>G	ENSP00000454971.2:p.Thr60=
ENST00000568375.2:c.116-3330A>G
ENST00000638185.1:n.1091A>G
ENST00000638210.1:n.1176A>G
ENST00000638705.1:c.876A>G	ENSP00000491223.1:p.Thr292=
ENST00000638836.1:n.786A>G
ENST00000639055.1:n.1597A>G
ENST00000639251.1:n.777A>G
ENST00000639268.1:c.511A>G
ENST00000639341.1:c.401A>G
ENST00000639770.1:c.914A>G	ENSP00000491999.1:n.914A>G
ENST00000640390.1:n.806A>G
ENST00000640469.1:c.240A>G	ENSP00000491875.1:p.Thr80=
ENST00000640560.1:n.652A>G
ENST00000640893.1:c.*274A>G	ENSP00000492677.1:n.*274A>G
ENST00000262493.10:c.876A>G	ENSP00000262493.6:p.Thr292=
ENST00000564727.1:c.96A>G	ENSP00000454971.1:p.Thr32=
ENST00000568375.1:n.116-3330A>G
NM_020988.2:c.876A>G	NP_066268.1:p.Thr292=
XM_011523003.1:c.750A>G	XP_011521305.1:p.Thr250=
XM_011523003.3:c.750A>G	XP_011521305.1:p.Thr250=
NM_020988.3:c.876A>G MANE Select	NP_066268.1:p.Thr292=