Canonical Allele Identifier: CA395955236

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388898A>G (hg19) ; chr16:g.56354986A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354986A>G , CM000678.2:g.56354986A>G	GRCh38
NC_000016.9:g.56388898A>G , CM000678.1:g.56388898A>G	GRCh37
NC_000016.8:g.54946399A>G	NCBI36
NG_042800.1:g.168648A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.998A>G MANE Select	ENSP00000262493.6:p.Gln333Arg
ENST00000562316.6:c.545-1117A>G	ENSP00000457238.2:n.545-1117A>G
ENST00000564727.2:c.302A>G	ENSP00000454971.2:p.Gln101Arg
ENST00000568375.2:c.236A>G
ENST00000638210.1:n.1298A>G
ENST00000638705.1:c.998A>G	ENSP00000491223.1:p.Gln333Arg
ENST00000638836.1:n.908A>G
ENST00000639251.1:n.899A>G
ENST00000639268.1:c.633A>G
ENST00000639341.1:c.523A>G
ENST00000639770.1:c.1036A>G	ENSP00000491999.1:n.1036A>G
ENST00000640390.1:n.928A>G
ENST00000640469.1:c.362A>G	ENSP00000491875.1:p.Gln121Arg
ENST00000640560.1:n.774A>G
ENST00000640893.1:c.*396A>G	ENSP00000492677.1:n.*396A>G
ENST00000262493.10:c.998A>G	ENSP00000262493.6:p.Gln333Arg
ENST00000564727.1:c.218A>G	ENSP00000454971.1:p.Gln73Arg
ENST00000568375.1:n.236A>G
NM_020988.2:c.998A>G	NP_066268.1:p.Gln333Arg
XM_011523003.1:c.872A>G	XP_011521305.1:p.Gln291Arg
XM_011523003.3:c.872A>G	XP_011521305.1:p.Gln291Arg
NM_020988.3:c.998A>G MANE Select	NP_066268.1:p.Gln333Arg