Canonical Allele Identifier: CA622304682
Gene: GNAO1 HGNC NCBI

Linked Data

dbSNP Id: rs1374758845

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56336633G>A , CM000678.2:g.56336633G>A GRCh38
NC_000016.9:g.56370545G>A , CM000678.1:g.56370545G>A GRCh37
NC_000016.8:g.54928046G>A NCBI36
NG_042800.1:g.150295G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262494.13:c.594-98G>A ENSP00000262494.7:n.594-98G>A
ENST00000262493.12:c.594-98G>A MANE Select ENSP00000262493.6:n.594-98G>A
ENST00000262494.12:c.594-98G>A ENSP00000262494.7:n.594-98G>A
ENST00000562316.6:c.261-98G>A ENSP00000457238.2:n.261-98G>A
ENST00000638185.1:n.809-98G>A
ENST00000638210.1:n.894-98G>A
ENST00000638705.1:c.594-98G>A ENSP00000491223.1:n.594-98G>A
ENST00000638836.1:n.504-98G>A
ENST00000639055.1:n.1315-98G>A
ENST00000639251.1:n.495-98G>A
ENST00000639268.1:c.229-98G>A
ENST00000639341.1:c.119-98G>A
ENST00000639770.1:c.632-98G>A ENSP00000491999.1:n.632-98G>A
ENST00000640390.1:n.524-98G>A
ENST00000640560.1:n.272G>A
ENST00000640893.1:c.433-98G>A ENSP00000492677.1:n.433-98G>A
ENST00000262493.10:c.594-98G>A ENSP00000262493.6:n.594-98G>A
ENST00000262494.11:c.594-98G>A ENSP00000262494.7:n.594-98G>A
NM_020988.2:c.594-98G>A NP_066268.1:n.594-98G>A
NM_138736.2:c.594-98G>A NP_620073.2:n.594-98G>A
XM_011523003.1:c.468-98G>A XP_011521305.1:n.468-98G>A
XM_011523003.3:c.468-98G>A XP_011521305.1:n.468-98G>A
NM_020988.3:c.594-98G>A MANE Select NP_066268.1:n.594-98G>A
NM_138736.3:c.594-98G>A NP_620073.2:n.594-98G>A