Canonical Allele Identifier: CA2224102553
Gene: GNAO1 HGNC NCBI

Linked Data

dbSNP Id: rs2037745806

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56336910_56336921del , CM000678.2:g.56336910_56336921del GRCh38
NC_000016.9:g.56370822_56370833del , CM000678.1:g.56370822_56370833del GRCh37
NC_000016.8:g.54928323_54928334del NCBI36
NG_042800.1:g.150572_150583del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262494.13:c.723+50_723+61del ENSP00000262494.7:n.723+50_723+61del
ENST00000262493.12:c.723+50_723+61del MANE Select ENSP00000262493.6:n.723+50_723+61del
ENST00000262494.12:c.723+50_723+61del ENSP00000262494.7:n.723+50_723+61del
ENST00000562316.6:c.390+50_390+61del ENSP00000457238.2:n.390+50_390+61del
ENST00000564727.2:c.27+50_27+61del ENSP00000454971.2:n.27+50_27+61del
ENST00000568375.2:c.115+50_115+61del
ENST00000638185.1:n.938+50_938+61del
ENST00000638210.1:n.1023+50_1023+61del
ENST00000638705.1:c.723+50_723+61del ENSP00000491223.1:n.723+50_723+61del
ENST00000638836.1:n.633+50_633+61del
ENST00000639055.1:n.1444+50_1444+61del
ENST00000639251.1:n.624+50_624+61del
ENST00000639268.1:c.358+50_358+61del
ENST00000639341.1:c.248+50_248+61del
ENST00000639770.1:c.761+50_761+61del ENSP00000491999.1:n.761+50_761+61del
ENST00000640390.1:n.653+50_653+61del
ENST00000640469.1:c.87+50_87+61del ENSP00000491875.1:n.87+50_87+61del
ENST00000640560.1:n.499+50_499+61del
ENST00000640893.1:c.*121+50_*121+61del ENSP00000492677.1:n.*121+50_*121+61del
ENST00000262493.10:c.723+50_723+61del ENSP00000262493.6:n.723+50_723+61del
ENST00000262494.11:c.723+50_723+61del ENSP00000262494.7:n.723+50_723+61del
ENST00000568375.1:n.115+50_115+61del
NM_020988.2:c.723+50_723+61del NP_066268.1:n.723+50_723+61del
NM_138736.2:c.723+50_723+61del NP_620073.2:n.723+50_723+61del
XM_011523003.1:c.597+50_597+61del XP_011521305.1:n.597+50_597+61del
XM_011523003.3:c.597+50_597+61del XP_011521305.1:n.597+50_597+61del
NM_020988.3:c.723+50_723+61del MANE Select NP_066268.1:n.723+50_723+61del
NM_138736.3:c.723+50_723+61del NP_620073.2:n.723+50_723+61del