Canonical Allele Identifier: CA395952198

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370674C>A (hg19) ; chr16:g.56336762C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336762C>A , CM000678.2:g.56336762C>A	GRCh38
NC_000016.9:g.56370674C>A , CM000678.1:g.56370674C>A	GRCh37
NC_000016.8:g.54928175C>A	NCBI36
NG_042800.1:g.150424C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.625C>A	ENSP00000262494.7:p.Arg209Ser
ENST00000262493.12:c.625C>A MANE Select	ENSP00000262493.6:p.Arg209Ser
ENST00000262494.12:c.625C>A	ENSP00000262494.7:p.Arg209Ser
ENST00000562316.6:c.292C>A	ENSP00000457238.2:p.Arg98Ser
ENST00000568375.2:c.17C>A
ENST00000638185.1:n.840C>A
ENST00000638210.1:n.925C>A
ENST00000638705.1:c.625C>A	ENSP00000491223.1:p.Arg209Ser
ENST00000638836.1:n.535C>A
ENST00000639055.1:n.1346C>A
ENST00000639251.1:n.526C>A
ENST00000639268.1:c.260C>A
ENST00000639341.1:c.150C>A
ENST00000639770.1:c.663C>A	ENSP00000491999.1:n.663C>A
ENST00000640390.1:n.555C>A
ENST00000640560.1:n.401C>A
ENST00000640893.1:c.*23C>A	ENSP00000492677.1:n.*23C>A
ENST00000262493.10:c.625C>A	ENSP00000262493.6:p.Arg209Ser
ENST00000262494.11:c.625C>A	ENSP00000262494.7:p.Arg209Ser
ENST00000568375.1:n.17C>A
NM_020988.2:c.625C>A	NP_066268.1:p.Arg209Ser
NM_138736.2:c.625C>A	NP_620073.2:p.Arg209Ser
XM_011523003.1:c.499C>A	XP_011521305.1:p.Arg167Ser
XM_011523003.3:c.499C>A	XP_011521305.1:p.Arg167Ser
NM_020988.3:c.625C>A MANE Select	NP_066268.1:p.Arg209Ser
NM_138736.3:c.625C>A	NP_620073.2:p.Arg209Ser