Canonical Allele Identifier: CA2224101568
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56334809C= , CM000678.2:g.56334809C= GRCh38
NC_000016.9:g.56368721C= , CM000678.1:g.56368721C= GRCh37
NC_000016.8:g.54926222C= NCBI36
NG_042800.1:g.148471C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262494.13:c.545C= ENSP00000262494.7:p.Thr182=
ENST00000262493.12:c.545C= MANE Select ENSP00000262493.6:p.Thr182=
ENST00000262494.12:c.545C= ENSP00000262494.7:p.Thr182=
ENST00000562316.6:c.212C= ENSP00000457238.2:p.Thr71=
ENST00000638185.1:n.760C=
ENST00000638210.1:n.845C=
ENST00000638705.1:c.545C= ENSP00000491223.1:p.Thr182=
ENST00000638836.1:n.455C=
ENST00000639055.1:n.1266C=
ENST00000639251.1:n.446C=
ENST00000639268.1:c.229-1922C=
ENST00000639341.1:c.70C=
ENST00000639770.1:c.583C= ENSP00000491999.1:n.583C=
ENST00000640390.1:n.475C=
ENST00000640893.1:c.384C= ENSP00000492677.1:p.Asn128=
ENST00000262493.10:c.545C= ENSP00000262493.6:p.Thr182=
ENST00000262494.11:c.545C= ENSP00000262494.7:p.Thr182=
ENST00000562316.5:c.284C= ENSP00000457238.1:p.Thr95=
NM_020988.2:c.545C= NP_066268.1:p.Thr182=
NM_138736.2:c.545C= NP_620073.2:p.Thr182=
XM_011523003.1:c.419C= XP_011521305.1:p.Thr140=
XM_011523003.3:c.419C= XP_011521305.1:p.Thr140=
NM_020988.3:c.545C= MANE Select NP_066268.1:p.Thr182=
NM_138736.3:c.545C= NP_620073.2:p.Thr182=