Canonical Allele Identifier: CA395954968

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388786A>G (hg19) ; chr16:g.56354874A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354874A>G , CM000678.2:g.56354874A>G	GRCh38
NC_000016.9:g.56388786A>G , CM000678.1:g.56388786A>G	GRCh37
NC_000016.8:g.54946287A>G	NCBI36
NG_042800.1:g.168536A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262493.12:c.886A>G MANE Select	ENSP00000262493.6:p.Thr296Ala
ENST00000562316.6:c.545-1229A>G	ENSP00000457238.2:n.545-1229A>G
ENST00000564727.2:c.190A>G	ENSP00000454971.2:p.Thr64Ala
ENST00000568375.2:c.124A>G
ENST00000638185.1:n.1101A>G
ENST00000638210.1:n.1186A>G
ENST00000638705.1:c.886A>G	ENSP00000491223.1:p.Thr296Ala
ENST00000638836.1:n.796A>G
ENST00000639055.1:n.1607A>G
ENST00000639251.1:n.787A>G
ENST00000639268.1:c.521A>G
ENST00000639341.1:c.411A>G
ENST00000639770.1:c.924A>G	ENSP00000491999.1:n.924A>G
ENST00000640390.1:n.816A>G
ENST00000640469.1:c.250A>G	ENSP00000491875.1:p.Thr84Ala
ENST00000640560.1:n.662A>G
ENST00000640893.1:c.*284A>G	ENSP00000492677.1:n.*284A>G
ENST00000262493.10:c.886A>G	ENSP00000262493.6:p.Thr296Ala
ENST00000564727.1:c.106A>G	ENSP00000454971.1:p.Thr36Ala
ENST00000568375.1:n.124A>G
NM_020988.2:c.886A>G	NP_066268.1:p.Thr296Ala
XM_011523003.1:c.760A>G	XP_011521305.1:p.Thr254Ala
XM_011523003.3:c.760A>G	XP_011521305.1:p.Thr254Ala
NM_020988.3:c.886A>G MANE Select	NP_066268.1:p.Thr296Ala