Canonical Allele Identifier: CA395955081

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388834A>G (hg19) ; chr16:g.56354922A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354922A>G , CM000678.2:g.56354922A>G	GRCh38
NC_000016.9:g.56388834A>G , CM000678.1:g.56388834A>G	GRCh37
NC_000016.8:g.54946335A>G	NCBI36
NG_042800.1:g.168584A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.934A>G MANE Select	ENSP00000262493.6:p.Asn312Asp
ENST00000562316.6:c.545-1181A>G	ENSP00000457238.2:n.545-1181A>G
ENST00000564727.2:c.238A>G	ENSP00000454971.2:p.Asn80Asp
ENST00000568375.2:c.172A>G
ENST00000638185.1:n.1149A>G
ENST00000638210.1:n.1234A>G
ENST00000638705.1:c.934A>G	ENSP00000491223.1:p.Asn312Asp
ENST00000638836.1:n.844A>G
ENST00000639055.1:n.1655A>G
ENST00000639251.1:n.835A>G
ENST00000639268.1:c.569A>G
ENST00000639341.1:c.459A>G
ENST00000639770.1:c.972A>G	ENSP00000491999.1:n.972A>G
ENST00000640390.1:n.864A>G
ENST00000640469.1:c.298A>G	ENSP00000491875.1:p.Asn100Asp
ENST00000640560.1:n.710A>G
ENST00000640893.1:c.*332A>G	ENSP00000492677.1:n.*332A>G
ENST00000262493.10:c.934A>G	ENSP00000262493.6:p.Asn312Asp
ENST00000564727.1:c.154A>G	ENSP00000454971.1:p.Asn52Asp
ENST00000568375.1:n.172A>G
NM_020988.2:c.934A>G	NP_066268.1:p.Asn312Asp
XM_011523003.1:c.808A>G	XP_011521305.1:p.Asn270Asp
XM_011523003.3:c.808A>G	XP_011521305.1:p.Asn270Asp
NM_020988.3:c.934A>G MANE Select	NP_066268.1:p.Asn312Asp