Canonical Allele Identifier: CA495573516

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56368728C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334816C>G , CM000678.2:g.56334816C>G	GRCh38
NC_000016.9:g.56368728C>G , CM000678.1:g.56368728C>G	GRCh37
NC_000016.8:g.54926229C>G	NCBI36
NG_042800.1:g.148478C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.552C>G	ENSP00000262494.7:p.Gly184=
ENST00000262493.12:c.552C>G MANE Select	ENSP00000262493.6:p.Gly184=
ENST00000262494.12:c.552C>G	ENSP00000262494.7:p.Gly184=
ENST00000562316.6:c.219C>G	ENSP00000457238.2:p.Gly73=
ENST00000638185.1:n.767C>G
ENST00000638210.1:n.852C>G
ENST00000638705.1:c.552C>G	ENSP00000491223.1:p.Gly184=
ENST00000638836.1:n.462C>G
ENST00000639055.1:n.1273C>G
ENST00000639251.1:n.453C>G
ENST00000639268.1:c.229-1915C>G
ENST00000639341.1:c.77C>G
ENST00000639770.1:c.590C>G	ENSP00000491999.1:n.590C>G
ENST00000640390.1:n.482C>G
ENST00000640893.1:c.391C>G	ENSP00000492677.1:p.His131Asp
ENST00000262493.10:c.552C>G	ENSP00000262493.6:p.Gly184=
ENST00000262494.11:c.552C>G	ENSP00000262494.7:p.Gly184=
ENST00000562316.5:c.291C>G	ENSP00000457238.1:p.Gly97=
NM_020988.2:c.552C>G	NP_066268.1:p.Gly184=
NM_138736.2:c.552C>G	NP_620073.2:p.Gly184=
XM_011523003.1:c.426C>G	XP_011521305.1:p.Gly142=
XM_011523003.3:c.426C>G	XP_011521305.1:p.Gly142=
NM_020988.3:c.552C>G MANE Select	NP_066268.1:p.Gly184=
NM_138736.3:c.552C>G	NP_620073.2:p.Gly184=