Canonical Allele Identifier: CA281428467

Gene: GNAO1

Linked Data

• dbSNP Id: rs386791061

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56337074_56337075delinsTT , CM000678.2:g.56337074_56337075delinsTT	GRCh38
NC_000016.9:g.56370986_56370987delinsTT , CM000678.1:g.56370986_56370987delinsTT	GRCh37
NC_000016.8:g.54928487_54928488delinsTT	NCBI36
NG_042800.1:g.150736_150737delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.723+214_723+215delinsTT	ENSP00000262494.7:n.723+214_723+215delinsTT
ENST00000262493.12:c.723+214_723+215delinsTT MANE Select	ENSP00000262493.6:n.723+214_723+215delinsTT
ENST00000262494.12:c.723+214_723+215delinsTT	ENSP00000262494.7:n.723+214_723+215delinsTT
ENST00000562316.6:c.390+214_390+215delinsTT	ENSP00000457238.2:n.390+214_390+215delinsTT
ENST00000564727.2:c.27+214_27+215delinsTT	ENSP00000454971.2:n.27+214_27+215delinsTT
ENST00000568375.2:c.115+214_115+215delinsTT
ENST00000638185.1:n.938+214_938+215delinsTT
ENST00000638210.1:n.1023+214_1023+215delinsTT
ENST00000638705.1:c.723+214_723+215delinsTT	ENSP00000491223.1:n.723+214_723+215delinsTT
ENST00000638836.1:n.633+214_633+215delinsTT
ENST00000639055.1:n.1444+214_1444+215delinsTT
ENST00000639251.1:n.624+214_624+215delinsTT
ENST00000639268.1:c.358+214_358+215delinsTT
ENST00000639341.1:c.248+214_248+215delinsTT
ENST00000639770.1:c.761+214_761+215delinsTT	ENSP00000491999.1:n.761+214_761+215delinsTT
ENST00000640390.1:n.653+214_653+215delinsTT
ENST00000640469.1:c.87+214_87+215delinsTT	ENSP00000491875.1:n.87+214_87+215delinsTT
ENST00000640560.1:n.499+214_499+215delinsTT
ENST00000640893.1:c.*121+214_*121+215delinsTT	ENSP00000492677.1:n.*121+214_*121+215delinsTT
ENST00000262493.10:c.723+214_723+215delinsTT	ENSP00000262493.6:n.723+214_723+215delinsTT
ENST00000262494.11:c.723+214_723+215delinsTT	ENSP00000262494.7:n.723+214_723+215delinsTT
ENST00000568375.1:n.115+214_115+215delinsTT
NM_020988.2:c.723+214_723+215delinsTT	NP_066268.1:n.723+214_723+215delinsTT
NM_138736.2:c.723+214_723+215delinsTT	NP_620073.2:n.723+214_723+215delinsTT
XM_011523003.1:c.597+214_597+215delinsTT	XP_011521305.1:n.597+214_597+215delinsTT
XM_011523003.3:c.597+214_597+215delinsTT	XP_011521305.1:n.597+214_597+215delinsTT
NM_020988.3:c.723+214_723+215delinsTT MANE Select	NP_066268.1:n.723+214_723+215delinsTT
NM_138736.3:c.723+214_723+215delinsTT	NP_620073.2:n.723+214_723+215delinsTT