Canonical Allele Identifier: CA395955066
Gene: GNAO1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56354916A>G , CM000678.2:g.56354916A>G GRCh38
NC_000016.9:g.56388828A>G , CM000678.1:g.56388828A>G GRCh37
NC_000016.8:g.54946329A>G NCBI36
NG_042800.1:g.168578A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262493.12:c.928A>G MANE Select ENSP00000262493.6:p.Ser310Gly
ENST00000562316.6:c.545-1187A>G ENSP00000457238.2:n.545-1187A>G
ENST00000564727.2:c.232A>G ENSP00000454971.2:p.Ser78Gly
ENST00000568375.2:c.166A>G
ENST00000638185.1:n.1143A>G
ENST00000638210.1:n.1228A>G
ENST00000638705.1:c.928A>G ENSP00000491223.1:p.Ser310Gly
ENST00000638836.1:n.838A>G
ENST00000639055.1:n.1649A>G
ENST00000639251.1:n.829A>G
ENST00000639268.1:c.563A>G
ENST00000639341.1:c.453A>G
ENST00000639770.1:c.966A>G ENSP00000491999.1:n.966A>G
ENST00000640390.1:n.858A>G
ENST00000640469.1:c.292A>G ENSP00000491875.1:p.Ser98Gly
ENST00000640560.1:n.704A>G
ENST00000640893.1:c.*326A>G ENSP00000492677.1:n.*326A>G
ENST00000262493.10:c.928A>G ENSP00000262493.6:p.Ser310Gly
ENST00000564727.1:c.148A>G ENSP00000454971.1:p.Ser50Gly
ENST00000568375.1:n.166A>G
NM_020988.2:c.928A>G NP_066268.1:p.Ser310Gly
XM_011523003.1:c.802A>G XP_011521305.1:p.Ser268Gly
XM_011523003.3:c.802A>G XP_011521305.1:p.Ser268Gly
NM_020988.3:c.928A>G MANE Select NP_066268.1:p.Ser310Gly