Canonical Allele Identifier: CA395954748

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385368A>G (hg19) ; chr16:g.56351456A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351456A>G , CM000678.2:g.56351456A>G	GRCh38
NC_000016.9:g.56385368A>G , CM000678.1:g.56385368A>G	GRCh37
NC_000016.8:g.54942869A>G	NCBI36
NG_042800.1:g.165118A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.796A>G MANE Select	ENSP00000262493.6:p.Ile266Val
ENST00000562316.6:c.463A>G	ENSP00000457238.2:p.Ile155Val
ENST00000564727.2:c.100A>G	ENSP00000454971.2:p.Ile34Val
ENST00000568375.2:c.116-3410A>G
ENST00000638185.1:n.1011A>G
ENST00000638210.1:n.1096A>G
ENST00000638705.1:c.796A>G	ENSP00000491223.1:p.Ile266Val
ENST00000638836.1:n.706A>G
ENST00000639055.1:n.1517A>G
ENST00000639251.1:n.697A>G
ENST00000639268.1:c.431A>G
ENST00000639341.1:c.321A>G
ENST00000639770.1:c.834A>G	ENSP00000491999.1:n.834A>G
ENST00000640390.1:n.726A>G
ENST00000640469.1:c.160A>G	ENSP00000491875.1:p.Ile54Val
ENST00000640560.1:n.572A>G
ENST00000640893.1:c.*194A>G	ENSP00000492677.1:n.*194A>G
ENST00000262493.10:c.796A>G	ENSP00000262493.6:p.Ile266Val
ENST00000564727.1:c.16A>G	ENSP00000454971.1:p.Ile6Val
ENST00000568375.1:n.116-3410A>G
NM_020988.2:c.796A>G	NP_066268.1:p.Ile266Val
XM_011523003.1:c.670A>G	XP_011521305.1:p.Ile224Val
XM_011523003.3:c.670A>G	XP_011521305.1:p.Ile224Val
NM_020988.3:c.796A>G MANE Select	NP_066268.1:p.Ile266Val