Canonical Allele Identifier: CA2224102487
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56336741G= , CM000678.2:g.56336741G= GRCh38
NC_000016.9:g.56370653G= , CM000678.1:g.56370653G= GRCh37
NC_000016.8:g.54928154G= NCBI36
NG_042800.1:g.150403G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262494.13:c.604G= ENSP00000262494.7:p.Val202=
ENST00000262493.12:c.604G= MANE Select ENSP00000262493.6:p.Val202=
ENST00000262494.12:c.604G= ENSP00000262494.7:p.Val202=
ENST00000562316.6:c.271G= ENSP00000457238.2:p.Val91=
ENST00000638185.1:n.819G=
ENST00000638210.1:n.904G=
ENST00000638705.1:c.604G= ENSP00000491223.1:p.Val202=
ENST00000638836.1:n.514G=
ENST00000639055.1:n.1325G=
ENST00000639251.1:n.505G=
ENST00000639268.1:c.239G=
ENST00000639341.1:c.129G=
ENST00000639770.1:c.642G= ENSP00000491999.1:n.642G=
ENST00000640390.1:n.534G=
ENST00000640560.1:n.380G=
ENST00000640893.1:c.*2G= ENSP00000492677.1:n.*2G=
ENST00000262493.10:c.604G= ENSP00000262493.6:p.Val202=
ENST00000262494.11:c.604G= ENSP00000262494.7:p.Val202=
NM_020988.2:c.604G= NP_066268.1:p.Val202=
NM_138736.2:c.604G= NP_620073.2:p.Val202=
XM_011523003.1:c.478G= XP_011521305.1:p.Val160=
XM_011523003.3:c.478G= XP_011521305.1:p.Val160=
NM_020988.3:c.604G= MANE Select NP_066268.1:p.Val202=
NM_138736.3:c.604G= NP_620073.2:p.Val202=