Canonical Allele Identifier: CA395952397
Gene: GNAO1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56336847A>G , CM000678.2:g.56336847A>G GRCh38
NC_000016.9:g.56370759A>G , CM000678.1:g.56370759A>G GRCh37
NC_000016.8:g.54928260A>G NCBI36
NG_042800.1:g.150509A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262494.13:c.710A>G ENSP00000262494.7:p.Glu237Gly
ENST00000262493.12:c.710A>G MANE Select ENSP00000262493.6:p.Glu237Gly
ENST00000262494.12:c.710A>G ENSP00000262494.7:p.Glu237Gly
ENST00000562316.6:c.377A>G ENSP00000457238.2:p.Glu126Gly
ENST00000564727.2:c.14A>G ENSP00000454971.2:p.Glu5Gly
ENST00000568375.2:c.102A>G
ENST00000638185.1:n.925A>G
ENST00000638210.1:n.1010A>G
ENST00000638705.1:c.710A>G ENSP00000491223.1:p.Glu237Gly
ENST00000638836.1:n.620A>G
ENST00000639055.1:n.1431A>G
ENST00000639251.1:n.611A>G
ENST00000639268.1:c.345A>G
ENST00000639341.1:c.235A>G
ENST00000639770.1:c.748A>G ENSP00000491999.1:n.748A>G
ENST00000640390.1:n.640A>G
ENST00000640469.1:c.74A>G ENSP00000491875.1:p.Glu25Gly
ENST00000640560.1:n.486A>G
ENST00000640893.1:c.*108A>G ENSP00000492677.1:n.*108A>G
ENST00000262493.10:c.710A>G ENSP00000262493.6:p.Glu237Gly
ENST00000262494.11:c.710A>G ENSP00000262494.7:p.Glu237Gly
ENST00000568375.1:n.102A>G
NM_020988.2:c.710A>G NP_066268.1:p.Glu237Gly
NM_138736.2:c.710A>G NP_620073.2:p.Glu237Gly
XM_011523003.1:c.584A>G XP_011521305.1:p.Glu195Gly
XM_011523003.3:c.584A>G XP_011521305.1:p.Glu195Gly
NM_020988.3:c.710A>G MANE Select NP_066268.1:p.Glu237Gly
NM_138736.3:c.710A>G NP_620073.2:p.Glu237Gly