Canonical Allele Identifier: CA2224108730
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56351396G= , CM000678.2:g.56351396G= GRCh38
NC_000016.9:g.56385308G= , CM000678.1:g.56385308G= GRCh37
NC_000016.8:g.54942809G= NCBI36
NG_042800.1:g.165058G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262493.12:c.736G= MANE Select ENSP00000262493.6:p.Glu246=
ENST00000562316.6:c.403G= ENSP00000457238.2:p.Glu135=
ENST00000564727.2:c.40G= ENSP00000454971.2:p.Glu14=
ENST00000568375.2:c.116-3470G=
ENST00000638185.1:n.951G=
ENST00000638210.1:n.1036G=
ENST00000638705.1:c.736G= ENSP00000491223.1:p.Glu246=
ENST00000638836.1:n.646G=
ENST00000639055.1:n.1457G=
ENST00000639251.1:n.637G=
ENST00000639268.1:c.371G=
ENST00000639341.1:c.261G=
ENST00000639770.1:c.774G= ENSP00000491999.1:n.774G=
ENST00000640390.1:n.666G=
ENST00000640469.1:c.100G= ENSP00000491875.1:p.Glu34=
ENST00000640560.1:n.512G=
ENST00000640893.1:c.*134G= ENSP00000492677.1:n.*134G=
ENST00000262493.10:c.736G= ENSP00000262493.6:p.Glu246=
ENST00000568375.1:n.116-3470G=
NM_020988.2:c.736G= NP_066268.1:p.Glu246=
XM_011523003.1:c.610G= XP_011521305.1:p.Glu204=
XM_011523003.3:c.610G= XP_011521305.1:p.Glu204=
NM_020988.3:c.736G= MANE Select NP_066268.1:p.Glu246=