Canonical Allele Identifier: CA2224101557

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334798C= , CM000678.2:g.56334798C=	GRCh38
NC_000016.9:g.56368710C= , CM000678.1:g.56368710C=	GRCh37
NC_000016.8:g.54926211C=	NCBI36
NG_042800.1:g.148460C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.534C=	ENSP00000262494.7:p.Thr178=
ENST00000262493.12:c.534C= MANE Select	ENSP00000262493.6:p.Thr178=
ENST00000262494.12:c.534C=	ENSP00000262494.7:p.Thr178=
ENST00000562316.6:c.201C=	ENSP00000457238.2:p.Thr67=
ENST00000638185.1:n.749C=
ENST00000638210.1:n.834C=
ENST00000638705.1:c.534C=	ENSP00000491223.1:p.Thr178=
ENST00000638836.1:n.444C=
ENST00000639055.1:n.1255C=
ENST00000639251.1:n.435C=
ENST00000639268.1:c.229-1933C=
ENST00000639341.1:c.59C=
ENST00000639770.1:c.572C=	ENSP00000491999.1:n.572C=
ENST00000640390.1:n.464C=
ENST00000640893.1:c.373C=	ENSP00000492677.1:p.Gln125=
ENST00000262493.10:c.534C=	ENSP00000262493.6:p.Thr178=
ENST00000262494.11:c.534C=	ENSP00000262494.7:p.Thr178=
ENST00000562316.5:c.273C=	ENSP00000457238.1:p.Thr91=
NM_020988.2:c.534C=	NP_066268.1:p.Thr178=
NM_138736.2:c.534C=	NP_620073.2:p.Thr178=
XM_011523003.1:c.408C=	XP_011521305.1:p.Thr136=
XM_011523003.3:c.408C=	XP_011521305.1:p.Thr136=
NM_020988.3:c.534C= MANE Select	NP_066268.1:p.Thr178=
NM_138736.3:c.534C=	NP_620073.2:p.Thr178=