Canonical Allele Identifier: CA2224102572

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336953_56336954delinsCA , CM000678.2:g.56336953_56336954delinsCA	GRCh38
NC_000016.9:g.56370865_56370866delinsCA , CM000678.1:g.56370865_56370866delinsCA	GRCh37
NC_000016.8:g.54928366_54928367delinsCA	NCBI36
NG_042800.1:g.150615_150616delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.723+93_723+94delinsCA	ENSP00000262494.7:n.723+93_723+94delinsCA
ENST00000262493.12:c.723+93_723+94delinsCA MANE Select	ENSP00000262493.6:n.723+93_723+94delinsCA
ENST00000262494.12:c.723+93_723+94delinsCA	ENSP00000262494.7:n.723+93_723+94delinsCA
ENST00000562316.6:c.390+93_390+94delinsCA	ENSP00000457238.2:n.390+93_390+94delinsCA
ENST00000564727.2:c.27+93_27+94delinsCA	ENSP00000454971.2:n.27+93_27+94delinsCA
ENST00000568375.2:c.115+93_115+94delinsCA
ENST00000638185.1:n.938+93_938+94delinsCA
ENST00000638210.1:n.1023+93_1023+94delinsCA
ENST00000638705.1:c.723+93_723+94delinsCA	ENSP00000491223.1:n.723+93_723+94delinsCA
ENST00000638836.1:n.633+93_633+94delinsCA
ENST00000639055.1:n.1444+93_1444+94delinsCA
ENST00000639251.1:n.624+93_624+94delinsCA
ENST00000639268.1:c.358+93_358+94delinsCA
ENST00000639341.1:c.248+93_248+94delinsCA
ENST00000639770.1:c.761+93_761+94delinsCA	ENSP00000491999.1:n.761+93_761+94delinsCA
ENST00000640390.1:n.653+93_653+94delinsCA
ENST00000640469.1:c.87+93_87+94delinsCA	ENSP00000491875.1:n.87+93_87+94delinsCA
ENST00000640560.1:n.499+93_499+94delinsCA
ENST00000640893.1:c.*121+93_*121+94delinsCA	ENSP00000492677.1:n.*121+93_*121+94delinsCA
ENST00000262493.10:c.723+93_723+94delinsCA	ENSP00000262493.6:n.723+93_723+94delinsCA
ENST00000262494.11:c.723+93_723+94delinsCA	ENSP00000262494.7:n.723+93_723+94delinsCA
ENST00000568375.1:n.115+93_115+94delinsCA
NM_020988.2:c.723+93_723+94delinsCA	NP_066268.1:n.723+93_723+94delinsCA
NM_138736.2:c.723+93_723+94delinsCA	NP_620073.2:n.723+93_723+94delinsCA
XM_011523003.1:c.597+93_597+94delinsCA	XP_011521305.1:n.597+93_597+94delinsCA
XM_011523003.3:c.597+93_597+94delinsCA	XP_011521305.1:n.597+93_597+94delinsCA
NM_020988.3:c.723+93_723+94delinsCA MANE Select	NP_066268.1:n.723+93_723+94delinsCA
NM_138736.3:c.723+93_723+94delinsCA	NP_620073.2:n.723+93_723+94delinsCA