Canonical Allele Identifier: CA395955320
Gene: GNAO1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56355007C>G , CM000678.2:g.56355007C>G GRCh38
NC_000016.9:g.56388919C>G , CM000678.1:g.56388919C>G GRCh37
NC_000016.8:g.54946420C>G NCBI36
NG_042800.1:g.168669C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262493.12:c.1019C>G MANE Select ENSP00000262493.6:p.Thr340Ser
ENST00000562316.6:c.545-1096C>G ENSP00000457238.2:n.545-1096C>G
ENST00000564727.2:c.303+20C>G ENSP00000454971.2:n.303+20C>G
ENST00000568375.2:c.257C>G
ENST00000638210.1:n.1319C>G
ENST00000638705.1:c.1019C>G ENSP00000491223.1:p.Thr340Ser
ENST00000638836.1:n.929C>G
ENST00000639251.1:n.920C>G
ENST00000639268.1:c.654C>G
ENST00000639341.1:c.544C>G
ENST00000639770.1:c.1057C>G ENSP00000491999.1:n.1057C>G
ENST00000640390.1:n.949C>G
ENST00000640469.1:c.383C>G ENSP00000491875.1:p.Thr128Ser
ENST00000640560.1:n.795C>G
ENST00000640893.1:c.*417C>G ENSP00000492677.1:n.*417C>G
ENST00000262493.10:c.1019C>G ENSP00000262493.6:p.Thr340Ser
ENST00000564727.1:c.239C>G ENSP00000454971.1:p.Thr80Ser
ENST00000568375.1:n.257C>G
NM_020988.2:c.1019C>G NP_066268.1:p.Thr340Ser
XM_011523003.1:c.893C>G XP_011521305.1:p.Thr298Ser
XM_011523003.3:c.893C>G XP_011521305.1:p.Thr298Ser
NM_020988.3:c.1019C>G MANE Select NP_066268.1:p.Thr340Ser