Canonical Allele Identifier: CA2224108768
Gene: GNAO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56351535C= , CM000678.2:g.56351535C= GRCh38
NC_000016.9:g.56385447C= , CM000678.1:g.56385447C= GRCh37
NC_000016.8:g.54942948C= NCBI36
NG_042800.1:g.165197C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262493.12:c.875C= MANE Select ENSP00000262493.6:p.Thr292=
ENST00000562316.6:c.542C= ENSP00000457238.2:p.Thr181=
ENST00000564727.2:c.179C= ENSP00000454971.2:p.Thr60=
ENST00000568375.2:c.116-3331C=
ENST00000638185.1:n.1090C=
ENST00000638210.1:n.1175C=
ENST00000638705.1:c.875C= ENSP00000491223.1:p.Thr292=
ENST00000638836.1:n.785C=
ENST00000639055.1:n.1596C=
ENST00000639251.1:n.776C=
ENST00000639268.1:c.510C=
ENST00000639341.1:c.400C=
ENST00000639770.1:c.913C= ENSP00000491999.1:n.913C=
ENST00000640390.1:n.805C=
ENST00000640469.1:c.239C= ENSP00000491875.1:p.Thr80=
ENST00000640560.1:n.651C=
ENST00000640893.1:c.*273C= ENSP00000492677.1:n.*273C=
ENST00000262493.10:c.875C= ENSP00000262493.6:p.Thr292=
ENST00000564727.1:c.95C= ENSP00000454971.1:p.Thr32=
ENST00000568375.1:n.116-3331C=
NM_020988.2:c.875C= NP_066268.1:p.Thr292=
XM_011523003.1:c.749C= XP_011521305.1:p.Thr250=
XM_011523003.3:c.749C= XP_011521305.1:p.Thr250=
NM_020988.3:c.875C= MANE Select NP_066268.1:p.Thr292=