Canonical Allele Identifier: CA395954678

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385339A>G (hg19) ; chr16:g.56351427A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351427A>G , CM000678.2:g.56351427A>G	GRCh38
NC_000016.9:g.56385339A>G , CM000678.1:g.56385339A>G	GRCh37
NC_000016.8:g.54942840A>G	NCBI36
NG_042800.1:g.165089A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.767A>G MANE Select	ENSP00000262493.6:p.Asn256Ser
ENST00000562316.6:c.434A>G	ENSP00000457238.2:p.Asn145Ser
ENST00000564727.2:c.71A>G	ENSP00000454971.2:p.Asn24Ser
ENST00000568375.2:c.116-3439A>G
ENST00000638185.1:n.982A>G
ENST00000638210.1:n.1067A>G
ENST00000638705.1:c.767A>G	ENSP00000491223.1:p.Asn256Ser
ENST00000638836.1:n.677A>G
ENST00000639055.1:n.1488A>G
ENST00000639251.1:n.668A>G
ENST00000639268.1:c.402A>G
ENST00000639341.1:c.292A>G
ENST00000639770.1:c.805A>G	ENSP00000491999.1:n.805A>G
ENST00000640390.1:n.697A>G
ENST00000640469.1:c.131A>G	ENSP00000491875.1:p.Asn44Ser
ENST00000640560.1:n.543A>G
ENST00000640893.1:c.*165A>G	ENSP00000492677.1:n.*165A>G
ENST00000262493.10:c.767A>G	ENSP00000262493.6:p.Asn256Ser
ENST00000568375.1:n.116-3439A>G
NM_020988.2:c.767A>G	NP_066268.1:p.Asn256Ser
XM_011523003.1:c.641A>G	XP_011521305.1:p.Asn214Ser
XM_011523003.3:c.641A>G	XP_011521305.1:p.Asn214Ser
NM_020988.3:c.767A>G MANE Select	NP_066268.1:p.Asn256Ser