Canonical Allele Identifier: CA495765704

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56192289G>A , CM000678.2:g.56192289G>A	GRCh38
NC_000016.9:g.56226201G>A , CM000678.1:g.56226201G>A	GRCh37
NC_000016.8:g.54783702G>A	NCBI36
NG_042800.1:g.5951G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.54G>A	ENSP00000262494.7:p.Ala18=
ENST00000262493.12:c.54G>A MANE Select	ENSP00000262493.6:p.Ala18=
ENST00000262494.12:c.54G>A	ENSP00000262494.7:p.Ala18=
ENST00000563661.2:c.54G>A	ENSP00000492694.1:p.Ala18=
ENST00000569295.6:c.54G>A	ENSP00000492271.1:p.Ala18=
ENST00000570235.2:c.54G>A	ENSP00000477740.2:p.Ala18=
ENST00000638705.1:c.54G>A	ENSP00000491223.1:p.Ala18=
ENST00000639770.1:c.21G>A	ENSP00000491999.1:p.Ala7=
ENST00000639966.1:n.69G>A
ENST00000640893.1:c.54G>A	ENSP00000492677.1:p.Ala18=
ENST00000675160.1:c.54G>A	ENSP00000502403.1:p.Ala18=
ENST00000262493.10:c.54G>A	ENSP00000262493.6:p.Ala18=
ENST00000262494.11:c.54G>A	ENSP00000262494.7:p.Ala18=
ENST00000563661.1:n.51G>A
ENST00000569295.5:n.276G>A
ENST00000570235.1:c.54G>A	ENSP00000477740.1:p.Ala18=
NM_020988.2:c.54G>A	NP_066268.1:p.Ala18=
NM_138736.2:c.54G>A	NP_620073.2:p.Ala18=
NM_020988.3:c.54G>A MANE Select	NP_066268.1:p.Ala18=
NM_138736.3:c.54G>A	NP_620073.2:p.Ala18=