Canonical Allele Identifier: CA395955107

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388846A>G (hg19) ; chr16:g.56354934A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354934A>G , CM000678.2:g.56354934A>G	GRCh38
NC_000016.9:g.56388846A>G , CM000678.1:g.56388846A>G	GRCh37
NC_000016.8:g.54946347A>G	NCBI36
NG_042800.1:g.168596A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.946A>G MANE Select	ENSP00000262493.6:p.Asn316Asp
ENST00000562316.6:c.545-1169A>G	ENSP00000457238.2:n.545-1169A>G
ENST00000564727.2:c.250A>G	ENSP00000454971.2:p.Asn84Asp
ENST00000568375.2:c.184A>G
ENST00000638185.1:n.1161A>G
ENST00000638210.1:n.1246A>G
ENST00000638705.1:c.946A>G	ENSP00000491223.1:p.Asn316Asp
ENST00000638836.1:n.856A>G
ENST00000639055.1:n.1667A>G
ENST00000639251.1:n.847A>G
ENST00000639268.1:c.581A>G
ENST00000639341.1:c.471A>G
ENST00000639770.1:c.984A>G	ENSP00000491999.1:n.984A>G
ENST00000640390.1:n.876A>G
ENST00000640469.1:c.310A>G	ENSP00000491875.1:p.Asn104Asp
ENST00000640560.1:n.722A>G
ENST00000640893.1:c.*344A>G	ENSP00000492677.1:n.*344A>G
ENST00000262493.10:c.946A>G	ENSP00000262493.6:p.Asn316Asp
ENST00000564727.1:c.166A>G	ENSP00000454971.1:p.Asn56Asp
ENST00000568375.1:n.184A>G
NM_020988.2:c.946A>G	NP_066268.1:p.Asn316Asp
XM_011523003.1:c.820A>G	XP_011521305.1:p.Asn274Asp
XM_011523003.3:c.820A>G	XP_011521305.1:p.Asn274Asp
NM_020988.3:c.946A>G MANE Select	NP_066268.1:p.Asn316Asp