Canonical Allele Identifier: CA395952272
Gene: GNAO1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56336791C>G , CM000678.2:g.56336791C>G GRCh38
NC_000016.9:g.56370703C>G , CM000678.1:g.56370703C>G GRCh37
NC_000016.8:g.54928204C>G NCBI36
NG_042800.1:g.150453C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262494.13:c.654C>G ENSP00000262494.7:p.Asp218Glu
ENST00000262493.12:c.654C>G MANE Select ENSP00000262493.6:p.Asp218Glu
ENST00000262494.12:c.654C>G ENSP00000262494.7:p.Asp218Glu
ENST00000562316.6:c.321C>G ENSP00000457238.2:p.Asp107Glu
ENST00000568375.2:c.46C>G
ENST00000638185.1:n.869C>G
ENST00000638210.1:n.954C>G
ENST00000638705.1:c.654C>G ENSP00000491223.1:p.Asp218Glu
ENST00000638836.1:n.564C>G
ENST00000639055.1:n.1375C>G
ENST00000639251.1:n.555C>G
ENST00000639268.1:c.289C>G
ENST00000639341.1:c.179C>G
ENST00000639770.1:c.692C>G ENSP00000491999.1:n.692C>G
ENST00000640390.1:n.584C>G
ENST00000640469.1:c.18C>G ENSP00000491875.1:p.Asp6Glu
ENST00000640560.1:n.430C>G
ENST00000640893.1:c.*52C>G ENSP00000492677.1:n.*52C>G
ENST00000262493.10:c.654C>G ENSP00000262493.6:p.Asp218Glu
ENST00000262494.11:c.654C>G ENSP00000262494.7:p.Asp218Glu
ENST00000568375.1:n.46C>G
NM_020988.2:c.654C>G NP_066268.1:p.Asp218Glu
NM_138736.2:c.654C>G NP_620073.2:p.Asp218Glu
XM_011523003.1:c.528C>G XP_011521305.1:p.Asp176Glu
XM_011523003.3:c.528C>G XP_011521305.1:p.Asp176Glu
NM_020988.3:c.654C>G MANE Select NP_066268.1:p.Asp218Glu
NM_138736.3:c.654C>G NP_620073.2:p.Asp218Glu