Canonical Allele Identifier: CA2575998017

Gene: GNAO1

Linked Data

• gnomAD v4: 16-56336642-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336642C>A , CM000678.2:g.56336642C>A	GRCh38
NC_000016.9:g.56370554C>A , CM000678.1:g.56370554C>A	GRCh37
NC_000016.8:g.54928055C>A	NCBI36
NG_042800.1:g.150304C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.594-89C>A	ENSP00000262494.7:n.594-89C>A
ENST00000262493.12:c.594-89C>A MANE Select	ENSP00000262493.6:n.594-89C>A
ENST00000262494.12:c.594-89C>A	ENSP00000262494.7:n.594-89C>A
ENST00000562316.6:c.261-89C>A	ENSP00000457238.2:n.261-89C>A
ENST00000638185.1:n.809-89C>A
ENST00000638210.1:n.894-89C>A
ENST00000638705.1:c.594-89C>A	ENSP00000491223.1:n.594-89C>A
ENST00000638836.1:n.504-89C>A
ENST00000639055.1:n.1315-89C>A
ENST00000639251.1:n.495-89C>A
ENST00000639268.1:c.229-89C>A
ENST00000639341.1:c.119-89C>A
ENST00000639770.1:c.632-89C>A	ENSP00000491999.1:n.632-89C>A
ENST00000640390.1:n.524-89C>A
ENST00000640560.1:n.281C>A
ENST00000640893.1:c.433-89C>A	ENSP00000492677.1:n.433-89C>A
ENST00000262493.10:c.594-89C>A	ENSP00000262493.6:n.594-89C>A
ENST00000262494.11:c.594-89C>A	ENSP00000262494.7:n.594-89C>A
NM_020988.2:c.594-89C>A	NP_066268.1:n.594-89C>A
NM_138736.2:c.594-89C>A	NP_620073.2:n.594-89C>A
XM_011523003.1:c.468-89C>A	XP_011521305.1:n.468-89C>A
XM_011523003.3:c.468-89C>A	XP_011521305.1:n.468-89C>A
NM_020988.3:c.594-89C>A MANE Select	NP_066268.1:n.594-89C>A
NM_138736.3:c.594-89C>A	NP_620073.2:n.594-89C>A