Canonical Allele Identifier: CA395954720

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385355C>G (hg19) ; chr16:g.56351443C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351443C>G , CM000678.2:g.56351443C>G	GRCh38
NC_000016.9:g.56385355C>G , CM000678.1:g.56385355C>G	GRCh37
NC_000016.8:g.54942856C>G	NCBI36
NG_042800.1:g.165105C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262493.12:c.783C>G MANE Select	ENSP00000262493.6:p.Ile261Met
ENST00000562316.6:c.450C>G	ENSP00000457238.2:p.Ile150Met
ENST00000564727.2:c.87C>G	ENSP00000454971.2:p.Ile29Met
ENST00000568375.2:c.116-3423C>G
ENST00000638185.1:n.998C>G
ENST00000638210.1:n.1083C>G
ENST00000638705.1:c.783C>G	ENSP00000491223.1:p.Ile261Met
ENST00000638836.1:n.693C>G
ENST00000639055.1:n.1504C>G
ENST00000639251.1:n.684C>G
ENST00000639268.1:c.418C>G
ENST00000639341.1:c.308C>G
ENST00000639770.1:c.821C>G	ENSP00000491999.1:n.821C>G
ENST00000640390.1:n.713C>G
ENST00000640469.1:c.147C>G	ENSP00000491875.1:p.Ile49Met
ENST00000640560.1:n.559C>G
ENST00000640893.1:c.*181C>G	ENSP00000492677.1:n.*181C>G
ENST00000262493.10:c.783C>G	ENSP00000262493.6:p.Ile261Met
ENST00000564727.1:c.3C>G	ENSP00000454971.1:p.Ile1Met
ENST00000568375.1:n.116-3423C>G
NM_020988.2:c.783C>G	NP_066268.1:p.Ile261Met
XM_011523003.1:c.657C>G	XP_011521305.1:p.Ile219Met
XM_011523003.3:c.657C>G	XP_011521305.1:p.Ile219Met
NM_020988.3:c.783C>G MANE Select	NP_066268.1:p.Ile261Met