Canonical Allele Identifier: CA395954681

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385340C>G (hg19) ; chr16:g.56351428C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351428C>G , CM000678.2:g.56351428C>G	GRCh38
NC_000016.9:g.56385340C>G , CM000678.1:g.56385340C>G	GRCh37
NC_000016.8:g.54942841C>G	NCBI36
NG_042800.1:g.165090C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.768C>G MANE Select	ENSP00000262493.6:p.Asn256Lys
ENST00000562316.6:c.435C>G	ENSP00000457238.2:p.Asn145Lys
ENST00000564727.2:c.72C>G	ENSP00000454971.2:p.Asn24Lys
ENST00000568375.2:c.116-3438C>G
ENST00000638185.1:n.983C>G
ENST00000638210.1:n.1068C>G
ENST00000638705.1:c.768C>G	ENSP00000491223.1:p.Asn256Lys
ENST00000638836.1:n.678C>G
ENST00000639055.1:n.1489C>G
ENST00000639251.1:n.669C>G
ENST00000639268.1:c.403C>G
ENST00000639341.1:c.293C>G
ENST00000639770.1:c.806C>G	ENSP00000491999.1:n.806C>G
ENST00000640390.1:n.698C>G
ENST00000640469.1:c.132C>G	ENSP00000491875.1:p.Asn44Lys
ENST00000640560.1:n.544C>G
ENST00000640893.1:c.*166C>G	ENSP00000492677.1:n.*166C>G
ENST00000262493.10:c.768C>G	ENSP00000262493.6:p.Asn256Lys
ENST00000568375.1:n.116-3438C>G
NM_020988.2:c.768C>G	NP_066268.1:p.Asn256Lys
XM_011523003.1:c.642C>G	XP_011521305.1:p.Asn214Lys
XM_011523003.3:c.642C>G	XP_011521305.1:p.Asn214Lys
NM_020988.3:c.768C>G MANE Select	NP_066268.1:p.Asn256Lys