Canonical Allele Identifier: CA396128208

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56276044G>A , CM000678.2:g.56276044G>A	GRCh38
NC_000016.9:g.56309956G>A , CM000678.1:g.56309956G>A	GRCh37
NC_000016.8:g.54867457G>A	NCBI36
NG_042800.1:g.89706G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.275G>A	ENSP00000262494.7:p.Gly92Asp
ENST00000262493.12:c.275G>A MANE Select	ENSP00000262493.6:p.Gly92Asp
ENST00000262494.12:c.275G>A	ENSP00000262494.7:p.Gly92Asp
ENST00000563661.2:c.275G>A	ENSP00000492694.1:p.Gly92Asp
ENST00000638185.1:n.490G>A
ENST00000638210.1:n.575G>A
ENST00000638705.1:c.275G>A	ENSP00000491223.1:p.Gly92Asp
ENST00000638836.1:n.185G>A
ENST00000639055.1:n.996G>A
ENST00000639251.1:n.176G>A
ENST00000639268.1:c.39G>A
ENST00000639770.1:c.313G>A	ENSP00000491999.1:n.313G>A
ENST00000639966.1:n.290G>A
ENST00000640390.1:n.205G>A
ENST00000640893.1:c.275G>A	ENSP00000492677.1:p.Gly92Asp
ENST00000262493.10:c.275G>A	ENSP00000262493.6:p.Gly92Asp
ENST00000262494.11:c.275G>A	ENSP00000262494.7:p.Gly92Asp
ENST00000562316.5:c.14G>A	ENSP00000457238.1:p.Gly5Asp
ENST00000563440.1:c.14G>A	ENSP00000455774.1:p.Gly5Asp
ENST00000563661.1:n.272G>A
ENST00000565363.5:c.149G>A	ENSP00000454728.1:p.Gly50Asp
NM_020988.2:c.275G>A	NP_066268.1:p.Gly92Asp
NM_138736.2:c.275G>A	NP_620073.2:p.Gly92Asp
XM_011523003.1:c.149G>A	XP_011521305.1:p.Gly50Asp
XM_011523003.3:c.149G>A	XP_011521305.1:p.Gly50Asp
NM_020988.3:c.275G>A MANE Select	NP_066268.1:p.Gly92Asp
NM_138736.3:c.275G>A	NP_620073.2:p.Gly92Asp