Canonical Allele Identifier: CA2695223532
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56336854_56336861del , CM000678.2:g.56336854_56336861del GRCh38
NC_000016.9:g.56370766_56370773del , CM000678.1:g.56370766_56370773del GRCh37
NC_000016.8:g.54928267_54928274del NCBI36
NG_042800.1:g.150516_150523del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262494.13:c.717_723+1del
ENST00000262493.12:c.717_723+1del
ENST00000262494.12:c.717_723+1del
ENST00000562316.6:c.384_390+1del
ENST00000564727.2:c.21_27+1del
ENST00000568375.2:c.109_115+1del
ENST00000638185.1:n.932_938+1del
ENST00000638210.1:n.1017_1023+1del
ENST00000638705.1:c.717_723+1del
ENST00000638836.1:n.627_633+1del
ENST00000639055.1:n.1438_1444+1del
ENST00000639251.1:n.618_624+1del
ENST00000639268.1:c.352_358+1del
ENST00000639341.1:c.242_248+1del
ENST00000639770.1:c.755_761+1del
ENST00000640390.1:n.647_653+1del
ENST00000640469.1:c.81_87+1del
ENST00000640560.1:n.493_499+1del
ENST00000640893.1:c.*115_*121+1del
ENST00000262493.10:c.717_723+1del
ENST00000262494.11:c.717_723+1del
ENST00000568375.1:n.109_115+1del
NM_020988.2:c.717_723+1del
NM_138736.2:c.717_723+1del
XM_011523003.1:c.591_597+1del
XM_011523003.3:c.591_597+1del
NM_020988.3:c.717_723+1del
NM_138736.3:c.717_723+1del