Canonical Allele Identifier: CA2224102539

Gene: GNAO1

Linked Data

• dbSNP Id: rs1263090753

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336888_56336890del , CM000678.2:g.56336888_56336890del	GRCh38
NC_000016.9:g.56370800_56370802del , CM000678.1:g.56370800_56370802del	GRCh37
NC_000016.8:g.54928301_54928303del	NCBI36
NG_042800.1:g.150550_150552del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.723+28_723+30del	ENSP00000262494.7:n.723+28_723+30del
ENST00000262493.12:c.723+28_723+30del MANE Select	ENSP00000262493.6:n.723+28_723+30del
ENST00000262494.12:c.723+28_723+30del	ENSP00000262494.7:n.723+28_723+30del
ENST00000562316.6:c.390+28_390+30del	ENSP00000457238.2:n.390+28_390+30del
ENST00000564727.2:c.27+28_27+30del	ENSP00000454971.2:n.27+28_27+30del
ENST00000568375.2:c.115+28_115+30del
ENST00000638185.1:n.938+28_938+30del
ENST00000638210.1:n.1023+28_1023+30del
ENST00000638705.1:c.723+28_723+30del	ENSP00000491223.1:n.723+28_723+30del
ENST00000638836.1:n.633+28_633+30del
ENST00000639055.1:n.1444+28_1444+30del
ENST00000639251.1:n.624+28_624+30del
ENST00000639268.1:c.358+28_358+30del
ENST00000639341.1:c.248+28_248+30del
ENST00000639770.1:c.761+28_761+30del	ENSP00000491999.1:n.761+28_761+30del
ENST00000640390.1:n.653+28_653+30del
ENST00000640469.1:c.87+28_87+30del	ENSP00000491875.1:n.87+28_87+30del
ENST00000640560.1:n.499+28_499+30del
ENST00000640893.1:c.*121+28_*121+30del	ENSP00000492677.1:n.*121+28_*121+30del
ENST00000262493.10:c.723+28_723+30del	ENSP00000262493.6:n.723+28_723+30del
ENST00000262494.11:c.723+28_723+30del	ENSP00000262494.7:n.723+28_723+30del
ENST00000568375.1:n.115+28_115+30del
NM_020988.2:c.723+28_723+30del	NP_066268.1:n.723+28_723+30del
NM_138736.2:c.723+28_723+30del	NP_620073.2:n.723+28_723+30del
XM_011523003.1:c.597+28_597+30del	XP_011521305.1:n.597+28_597+30del
XM_011523003.3:c.597+28_597+30del	XP_011521305.1:n.597+28_597+30del
NM_020988.3:c.723+28_723+30del MANE Select	NP_066268.1:n.723+28_723+30del
NM_138736.3:c.723+28_723+30del	NP_620073.2:n.723+28_723+30del