Canonical Allele Identifier: CA395952248

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370694C>A (hg19) ; chr16:g.56336782C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336782C>A , CM000678.2:g.56336782C>A	GRCh38
NC_000016.9:g.56370694C>A , CM000678.1:g.56370694C>A	GRCh37
NC_000016.8:g.54928195C>A	NCBI36
NG_042800.1:g.150444C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.645C>A	ENSP00000262494.7:p.Cys215Ter
ENST00000262493.12:c.645C>A MANE Select	ENSP00000262493.6:p.Cys215Ter
ENST00000262494.12:c.645C>A	ENSP00000262494.7:p.Cys215Ter
ENST00000562316.6:c.312C>A	ENSP00000457238.2:p.Cys104Ter
ENST00000568375.2:c.37C>A
ENST00000638185.1:n.860C>A
ENST00000638210.1:n.945C>A
ENST00000638705.1:c.645C>A	ENSP00000491223.1:p.Cys215Ter
ENST00000638836.1:n.555C>A
ENST00000639055.1:n.1366C>A
ENST00000639251.1:n.546C>A
ENST00000639268.1:c.280C>A
ENST00000639341.1:c.170C>A
ENST00000639770.1:c.683C>A	ENSP00000491999.1:n.683C>A
ENST00000640390.1:n.575C>A
ENST00000640469.1:c.9C>A	ENSP00000491875.1:p.Cys3Ter
ENST00000640560.1:n.421C>A
ENST00000640893.1:c.*43C>A	ENSP00000492677.1:n.*43C>A
ENST00000262493.10:c.645C>A	ENSP00000262493.6:p.Cys215Ter
ENST00000262494.11:c.645C>A	ENSP00000262494.7:p.Cys215Ter
ENST00000568375.1:n.37C>A
NM_020988.2:c.645C>A	NP_066268.1:p.Cys215Ter
NM_138736.2:c.645C>A	NP_620073.2:p.Cys215Ter
XM_011523003.1:c.519C>A	XP_011521305.1:p.Cys173Ter
XM_011523003.3:c.519C>A	XP_011521305.1:p.Cys173Ter
NM_020988.3:c.645C>A MANE Select	NP_066268.1:p.Cys215Ter
NM_138736.3:c.645C>A	NP_620073.2:p.Cys215Ter