Canonical Allele Identifier: CA645293896
Gene: GNAO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 426965
dbSNP Id: rs1085307876

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56351376G>A , CM000678.2:g.56351376G>A GRCh38
NC_000016.9:g.56385288G>A , CM000678.1:g.56385288G>A GRCh37
NC_000016.8:g.54942789G>A NCBI36
NG_042800.1:g.165038G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262493.12:c.724-8G>A MANE Select ENSP00000262493.6:n.724-8G>A
ENST00000562316.6:c.391-8G>A ENSP00000457238.2:n.391-8G>A
ENST00000564727.2:c.28-8G>A ENSP00000454971.2:n.28-8G>A
ENST00000568375.2:c.116-3490G>A
ENST00000638185.1:n.939-8G>A
ENST00000638210.1:n.1024-8G>A
ENST00000638705.1:c.724-8G>A ENSP00000491223.1:n.724-8G>A
ENST00000638836.1:n.634-8G>A
ENST00000639055.1:n.1445-8G>A
ENST00000639251.1:n.625-8G>A
ENST00000639268.1:c.359-8G>A
ENST00000639341.1:c.249-8G>A
ENST00000639770.1:c.762-8G>A ENSP00000491999.1:n.762-8G>A
ENST00000640390.1:n.654-8G>A
ENST00000640469.1:c.88-8G>A ENSP00000491875.1:n.88-8G>A
ENST00000640560.1:n.500-8G>A
ENST00000640893.1:c.*122-8G>A ENSP00000492677.1:n.*122-8G>A
ENST00000262493.10:c.724-8G>A ENSP00000262493.6:n.724-8G>A
ENST00000568375.1:n.116-3490G>A
NM_020988.2:c.724-8G>A NP_066268.1:n.724-8G>A
XM_011523003.1:c.598-8G>A XP_011521305.1:n.598-8G>A
XM_011523003.3:c.598-8G>A XP_011521305.1:n.598-8G>A
NM_020988.3:c.724-8G>A MANE Select NP_066268.1:n.724-8G>A