Canonical Allele Identifier: CA2224102486
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56336740C= , CM000678.2:g.56336740C= GRCh38
NC_000016.9:g.56370652C= , CM000678.1:g.56370652C= GRCh37
NC_000016.8:g.54928153C= NCBI36
NG_042800.1:g.150402C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262494.13:c.603C= ENSP00000262494.7:p.Asp201=
ENST00000262493.12:c.603C= MANE Select ENSP00000262493.6:p.Asp201=
ENST00000262494.12:c.603C= ENSP00000262494.7:p.Asp201=
ENST00000562316.6:c.270C= ENSP00000457238.2:p.Asp90=
ENST00000638185.1:n.818C=
ENST00000638210.1:n.903C=
ENST00000638705.1:c.603C= ENSP00000491223.1:p.Asp201=
ENST00000638836.1:n.513C=
ENST00000639055.1:n.1324C=
ENST00000639251.1:n.504C=
ENST00000639268.1:c.238C=
ENST00000639341.1:c.128C=
ENST00000639770.1:c.641C= ENSP00000491999.1:n.641C=
ENST00000640390.1:n.533C=
ENST00000640560.1:n.379C=
ENST00000640893.1:c.*1C= ENSP00000492677.1:n.*1C=
ENST00000262493.10:c.603C= ENSP00000262493.6:p.Asp201=
ENST00000262494.11:c.603C= ENSP00000262494.7:p.Asp201=
NM_020988.2:c.603C= NP_066268.1:p.Asp201=
NM_138736.2:c.603C= NP_620073.2:p.Asp201=
XM_011523003.1:c.477C= XP_011521305.1:p.Asp159=
XM_011523003.3:c.477C= XP_011521305.1:p.Asp159=
NM_020988.3:c.603C= MANE Select NP_066268.1:p.Asp201=
NM_138736.3:c.603C= NP_620073.2:p.Asp201=