Canonical Allele Identifier: CA2224108742
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56351443C= , CM000678.2:g.56351443C= GRCh38
NC_000016.9:g.56385355C= , CM000678.1:g.56385355C= GRCh37
NC_000016.8:g.54942856C= NCBI36
NG_042800.1:g.165105C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262493.12:c.783C= MANE Select ENSP00000262493.6:p.Ile261=
ENST00000562316.6:c.450C= ENSP00000457238.2:p.Ile150=
ENST00000564727.2:c.87C= ENSP00000454971.2:p.Ile29=
ENST00000568375.2:c.116-3423C=
ENST00000638185.1:n.998C=
ENST00000638210.1:n.1083C=
ENST00000638705.1:c.783C= ENSP00000491223.1:p.Ile261=
ENST00000638836.1:n.693C=
ENST00000639055.1:n.1504C=
ENST00000639251.1:n.684C=
ENST00000639268.1:c.418C=
ENST00000639341.1:c.308C=
ENST00000639770.1:c.821C= ENSP00000491999.1:n.821C=
ENST00000640390.1:n.713C=
ENST00000640469.1:c.147C= ENSP00000491875.1:p.Ile49=
ENST00000640560.1:n.559C=
ENST00000640893.1:c.*181C= ENSP00000492677.1:n.*181C=
ENST00000262493.10:c.783C= ENSP00000262493.6:p.Ile261=
ENST00000564727.1:c.3C= ENSP00000454971.1:p.Ile1=
ENST00000568375.1:n.116-3423C=
NM_020988.2:c.783C= NP_066268.1:p.Ile261=
XM_011523003.1:c.657C= XP_011521305.1:p.Ile219=
XM_011523003.3:c.657C= XP_011521305.1:p.Ile219=
NM_020988.3:c.783C= MANE Select NP_066268.1:p.Ile261=