Canonical Allele Identifier: CA2224102489
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56336744G= , CM000678.2:g.56336744G= GRCh38
NC_000016.9:g.56370656G= , CM000678.1:g.56370656G= GRCh37
NC_000016.8:g.54928157G= NCBI36
NG_042800.1:g.150406G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262494.13:c.607G= ENSP00000262494.7:p.Gly203=
ENST00000262493.12:c.607G= MANE Select ENSP00000262493.6:p.Gly203=
ENST00000262494.12:c.607G= ENSP00000262494.7:p.Gly203=
ENST00000562316.6:c.274G= ENSP00000457238.2:p.Gly92=
ENST00000638185.1:n.822G=
ENST00000638210.1:n.907G=
ENST00000638705.1:c.607G= ENSP00000491223.1:p.Gly203=
ENST00000638836.1:n.517G=
ENST00000639055.1:n.1328G=
ENST00000639251.1:n.508G=
ENST00000639268.1:c.242G=
ENST00000639341.1:c.132G=
ENST00000639770.1:c.645G= ENSP00000491999.1:n.645G=
ENST00000640390.1:n.537G=
ENST00000640560.1:n.383G=
ENST00000640893.1:c.*5G= ENSP00000492677.1:n.*5G=
ENST00000262493.10:c.607G= ENSP00000262493.6:p.Gly203=
ENST00000262494.11:c.607G= ENSP00000262494.7:p.Gly203=
NM_020988.2:c.607G= NP_066268.1:p.Gly203=
NM_138736.2:c.607G= NP_620073.2:p.Gly203=
XM_011523003.1:c.481G= XP_011521305.1:p.Gly161=
XM_011523003.3:c.481G= XP_011521305.1:p.Gly161=
NM_020988.3:c.607G= MANE Select NP_066268.1:p.Gly203=
NM_138736.3:c.607G= NP_620073.2:p.Gly203=