Canonical Allele Identifier: CA2224102537

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336885_56336888delinsAGGG , CM000678.2:g.56336885_56336888delinsAGGG	GRCh38
NC_000016.9:g.56370797_56370800delinsAGGG , CM000678.1:g.56370797_56370800delinsAGGG	GRCh37
NC_000016.8:g.54928298_54928301delinsAGGG	NCBI36
NG_042800.1:g.150547_150550delinsAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.723+25_723+28delinsAGGG	ENSP00000262494.7:n.723+25_723+28delinsAGGG
ENST00000262493.12:c.723+25_723+28delinsAGGG MANE Select	ENSP00000262493.6:n.723+25_723+28delinsAGGG
ENST00000262494.12:c.723+25_723+28delinsAGGG	ENSP00000262494.7:n.723+25_723+28delinsAGGG
ENST00000562316.6:c.390+25_390+28delinsAGGG	ENSP00000457238.2:n.390+25_390+28delinsAGGG
ENST00000564727.2:c.27+25_27+28delinsAGGG	ENSP00000454971.2:n.27+25_27+28delinsAGGG
ENST00000568375.2:c.115+25_115+28delinsAGGG
ENST00000638185.1:n.938+25_938+28delinsAGGG
ENST00000638210.1:n.1023+25_1023+28delinsAGGG
ENST00000638705.1:c.723+25_723+28delinsAGGG	ENSP00000491223.1:n.723+25_723+28delinsAGGG
ENST00000638836.1:n.633+25_633+28delinsAGGG
ENST00000639055.1:n.1444+25_1444+28delinsAGGG
ENST00000639251.1:n.624+25_624+28delinsAGGG
ENST00000639268.1:c.358+25_358+28delinsAGGG
ENST00000639341.1:c.248+25_248+28delinsAGGG
ENST00000639770.1:c.761+25_761+28delinsAGGG	ENSP00000491999.1:n.761+25_761+28delinsAGGG
ENST00000640390.1:n.653+25_653+28delinsAGGG
ENST00000640469.1:c.87+25_87+28delinsAGGG	ENSP00000491875.1:n.87+25_87+28delinsAGGG
ENST00000640560.1:n.499+25_499+28delinsAGGG
ENST00000640893.1:c.*121+25_*121+28delinsAGGG	ENSP00000492677.1:n.*121+25_*121+28delinsAGGG
ENST00000262493.10:c.723+25_723+28delinsAGGG	ENSP00000262493.6:n.723+25_723+28delinsAGGG
ENST00000262494.11:c.723+25_723+28delinsAGGG	ENSP00000262494.7:n.723+25_723+28delinsAGGG
ENST00000568375.1:n.115+25_115+28delinsAGGG
NM_020988.2:c.723+25_723+28delinsAGGG	NP_066268.1:n.723+25_723+28delinsAGGG
NM_138736.2:c.723+25_723+28delinsAGGG	NP_620073.2:n.723+25_723+28delinsAGGG
XM_011523003.1:c.597+25_597+28delinsAGGG	XP_011521305.1:n.597+25_597+28delinsAGGG
XM_011523003.3:c.597+25_597+28delinsAGGG	XP_011521305.1:n.597+25_597+28delinsAGGG
NM_020988.3:c.723+25_723+28delinsAGGG MANE Select	NP_066268.1:n.723+25_723+28delinsAGGG
NM_138736.3:c.723+25_723+28delinsAGGG	NP_620073.2:n.723+25_723+28delinsAGGG