Canonical Allele Identifier: CA2840732407

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336879_56336880insTGCC , CM000678.2:g.56336879_56336880insTGCC	GRCh38
NC_000016.9:g.56370791_56370792insTGCC , CM000678.1:g.56370791_56370792insTGCC	GRCh37
NC_000016.8:g.54928292_54928293insTGCC	NCBI36
NG_042800.1:g.150541_150542insTGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.723+19_723+20insTGCC	ENSP00000262494.7:n.723+19_723+20insTGCC
ENST00000262493.12:c.723+19_723+20insTGCC MANE Select	ENSP00000262493.6:n.723+19_723+20insTGCC
ENST00000262494.12:c.723+19_723+20insTGCC	ENSP00000262494.7:n.723+19_723+20insTGCC
ENST00000562316.6:c.390+19_390+20insTGCC	ENSP00000457238.2:n.390+19_390+20insTGCC
ENST00000564727.2:c.27+19_27+20insTGCC	ENSP00000454971.2:n.27+19_27+20insTGCC
ENST00000568375.2:c.115+19_115+20insTGCC
ENST00000638185.1:n.938+19_938+20insTGCC
ENST00000638210.1:n.1023+19_1023+20insTGCC
ENST00000638705.1:c.723+19_723+20insTGCC	ENSP00000491223.1:n.723+19_723+20insTGCC
ENST00000638836.1:n.633+19_633+20insTGCC
ENST00000639055.1:n.1444+19_1444+20insTGCC
ENST00000639251.1:n.624+19_624+20insTGCC
ENST00000639268.1:c.358+19_358+20insTGCC
ENST00000639341.1:c.248+19_248+20insTGCC
ENST00000639770.1:c.761+19_761+20insTGCC	ENSP00000491999.1:n.761+19_761+20insTGCC
ENST00000640390.1:n.653+19_653+20insTGCC
ENST00000640469.1:c.87+19_87+20insTGCC	ENSP00000491875.1:n.87+19_87+20insTGCC
ENST00000640560.1:n.499+19_499+20insTGCC
ENST00000640893.1:c.*121+19_*121+20insTGCC	ENSP00000492677.1:n.*121+19_*121+20insTGCC
ENST00000262493.10:c.723+19_723+20insTGCC	ENSP00000262493.6:n.723+19_723+20insTGCC
ENST00000262494.11:c.723+19_723+20insTGCC	ENSP00000262494.7:n.723+19_723+20insTGCC
ENST00000568375.1:n.115+19_115+20insTGCC
NM_020988.2:c.723+19_723+20insTGCC	NP_066268.1:n.723+19_723+20insTGCC
NM_138736.2:c.723+19_723+20insTGCC	NP_620073.2:n.723+19_723+20insTGCC
XM_011523003.1:c.597+19_597+20insTGCC	XP_011521305.1:n.597+19_597+20insTGCC
XM_011523003.3:c.597+19_597+20insTGCC	XP_011521305.1:n.597+19_597+20insTGCC
NM_020988.3:c.723+19_723+20insTGCC MANE Select	NP_066268.1:n.723+19_723+20insTGCC
NM_138736.3:c.723+19_723+20insTGCC	NP_620073.2:n.723+19_723+20insTGCC