Canonical Allele Identifier: CA2224108731
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56351397A= , CM000678.2:g.56351397A= GRCh38
NC_000016.9:g.56385309A= , CM000678.1:g.56385309A= GRCh37
NC_000016.8:g.54942810A= NCBI36
NG_042800.1:g.165059A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262493.12:c.737A= MANE Select ENSP00000262493.6:p.Glu246=
ENST00000562316.6:c.404A= ENSP00000457238.2:p.Glu135=
ENST00000564727.2:c.41A= ENSP00000454971.2:p.Glu14=
ENST00000568375.2:c.116-3469A=
ENST00000638185.1:n.952A=
ENST00000638210.1:n.1037A=
ENST00000638705.1:c.737A= ENSP00000491223.1:p.Glu246=
ENST00000638836.1:n.647A=
ENST00000639055.1:n.1458A=
ENST00000639251.1:n.638A=
ENST00000639268.1:c.372A=
ENST00000639341.1:c.262A=
ENST00000639770.1:c.775A= ENSP00000491999.1:n.775A=
ENST00000640390.1:n.667A=
ENST00000640469.1:c.101A= ENSP00000491875.1:p.Glu34=
ENST00000640560.1:n.513A=
ENST00000640893.1:c.*135A= ENSP00000492677.1:n.*135A=
ENST00000262493.10:c.737A= ENSP00000262493.6:p.Glu246=
ENST00000568375.1:n.116-3469A=
NM_020988.2:c.737A= NP_066268.1:p.Glu246=
XM_011523003.1:c.611A= XP_011521305.1:p.Glu204=
XM_011523003.3:c.611A= XP_011521305.1:p.Glu204=
NM_020988.3:c.737A= MANE Select NP_066268.1:p.Glu246=