Canonical Allele Identifier: CA395952339

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370734A>G (hg19) ; chr16:g.56336822A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336822A>G , CM000678.2:g.56336822A>G	GRCh38
NC_000016.9:g.56370734A>G , CM000678.1:g.56370734A>G	GRCh37
NC_000016.8:g.54928235A>G	NCBI36
NG_042800.1:g.150484A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262494.13:c.685A>G	ENSP00000262494.7:p.Ser229Gly
ENST00000262493.12:c.685A>G MANE Select	ENSP00000262493.6:p.Ser229Gly
ENST00000262494.12:c.685A>G	ENSP00000262494.7:p.Ser229Gly
ENST00000562316.6:c.352A>G	ENSP00000457238.2:p.Ser118Gly
ENST00000568375.2:c.77A>G
ENST00000638185.1:n.900A>G
ENST00000638210.1:n.985A>G
ENST00000638705.1:c.685A>G	ENSP00000491223.1:p.Ser229Gly
ENST00000638836.1:n.595A>G
ENST00000639055.1:n.1406A>G
ENST00000639251.1:n.586A>G
ENST00000639268.1:c.320A>G
ENST00000639341.1:c.210A>G
ENST00000639770.1:c.723A>G	ENSP00000491999.1:n.723A>G
ENST00000640390.1:n.615A>G
ENST00000640469.1:c.49A>G	ENSP00000491875.1:p.Ser17Gly
ENST00000640560.1:n.461A>G
ENST00000640893.1:c.*83A>G	ENSP00000492677.1:n.*83A>G
ENST00000262493.10:c.685A>G	ENSP00000262493.6:p.Ser229Gly
ENST00000262494.11:c.685A>G	ENSP00000262494.7:p.Ser229Gly
ENST00000568375.1:n.77A>G
NM_020988.2:c.685A>G	NP_066268.1:p.Ser229Gly
NM_138736.2:c.685A>G	NP_620073.2:p.Ser229Gly
XM_011523003.1:c.559A>G	XP_011521305.1:p.Ser187Gly
XM_011523003.3:c.559A>G	XP_011521305.1:p.Ser187Gly
NM_020988.3:c.685A>G MANE Select	NP_066268.1:p.Ser229Gly
NM_138736.3:c.685A>G	NP_620073.2:p.Ser229Gly