Canonical Allele Identifier: CA2224102658

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56337120_56337121delinsCT , CM000678.2:g.56337120_56337121delinsCT	GRCh38
NC_000016.9:g.56371032_56371033delinsCT , CM000678.1:g.56371032_56371033delinsCT	GRCh37
NC_000016.8:g.54928533_54928534delinsCT	NCBI36
NG_042800.1:g.150782_150783delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.723+260_723+261delinsCT	ENSP00000262494.7:n.723+260_723+261delinsCT
ENST00000262493.12:c.723+260_723+261delinsCT MANE Select	ENSP00000262493.6:n.723+260_723+261delinsCT
ENST00000262494.12:c.723+260_723+261delinsCT	ENSP00000262494.7:n.723+260_723+261delinsCT
ENST00000562316.6:c.390+260_390+261delinsCT	ENSP00000457238.2:n.390+260_390+261delinsCT
ENST00000564727.2:c.27+260_27+261delinsCT	ENSP00000454971.2:n.27+260_27+261delinsCT
ENST00000568375.2:c.115+260_115+261delinsCT
ENST00000638185.1:n.938+260_938+261delinsCT
ENST00000638210.1:n.1023+260_1023+261delinsCT
ENST00000638705.1:c.723+260_723+261delinsCT	ENSP00000491223.1:n.723+260_723+261delinsCT
ENST00000638836.1:n.633+260_633+261delinsCT
ENST00000639055.1:n.1444+260_1444+261delinsCT
ENST00000639251.1:n.624+260_624+261delinsCT
ENST00000639268.1:c.358+260_358+261delinsCT
ENST00000639341.1:c.248+260_248+261delinsCT
ENST00000639770.1:c.761+260_761+261delinsCT	ENSP00000491999.1:n.761+260_761+261delinsCT
ENST00000640390.1:n.653+260_653+261delinsCT
ENST00000640469.1:c.87+260_87+261delinsCT	ENSP00000491875.1:n.87+260_87+261delinsCT
ENST00000640560.1:n.499+260_499+261delinsCT
ENST00000640893.1:c.*121+260_*121+261delinsCT	ENSP00000492677.1:n.*121+260_*121+261delinsCT
ENST00000262493.10:c.723+260_723+261delinsCT	ENSP00000262493.6:n.723+260_723+261delinsCT
ENST00000262494.11:c.723+260_723+261delinsCT	ENSP00000262494.7:n.723+260_723+261delinsCT
ENST00000568375.1:n.115+260_115+261delinsCT
NM_020988.2:c.723+260_723+261delinsCT	NP_066268.1:n.723+260_723+261delinsCT
NM_138736.2:c.723+260_723+261delinsCT	NP_620073.2:n.723+260_723+261delinsCT
XM_011523003.1:c.597+260_597+261delinsCT	XP_011521305.1:n.597+260_597+261delinsCT
XM_011523003.3:c.597+260_597+261delinsCT	XP_011521305.1:n.597+260_597+261delinsCT
NM_020988.3:c.723+260_723+261delinsCT MANE Select	NP_066268.1:n.723+260_723+261delinsCT
NM_138736.3:c.723+260_723+261delinsCT	NP_620073.2:n.723+260_723+261delinsCT