Canonical Allele Identifier: CA2224102481

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336722C= , CM000678.2:g.56336722C=	GRCh38
NC_000016.9:g.56370634C= , CM000678.1:g.56370634C=	GRCh37
NC_000016.8:g.54928135C=	NCBI36
NG_042800.1:g.150384C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.594-9C=	ENSP00000262494.7:n.594-9C=
ENST00000262493.12:c.594-9C= MANE Select	ENSP00000262493.6:n.594-9C=
ENST00000262494.12:c.594-9C=	ENSP00000262494.7:n.594-9C=
ENST00000562316.6:c.261-9C=	ENSP00000457238.2:n.261-9C=
ENST00000638185.1:n.809-9C=
ENST00000638210.1:n.894-9C=
ENST00000638705.1:c.594-9C=	ENSP00000491223.1:n.594-9C=
ENST00000638836.1:n.504-9C=
ENST00000639055.1:n.1315-9C=
ENST00000639251.1:n.495-9C=
ENST00000639268.1:c.229-9C=
ENST00000639341.1:c.119-9C=
ENST00000639770.1:c.632-9C=	ENSP00000491999.1:n.632-9C=
ENST00000640390.1:n.524-9C=
ENST00000640560.1:n.361C=
ENST00000640893.1:c.433-9C=	ENSP00000492677.1:n.433-9C=
ENST00000262493.10:c.594-9C=	ENSP00000262493.6:n.594-9C=
ENST00000262494.11:c.594-9C=	ENSP00000262494.7:n.594-9C=
NM_020988.2:c.594-9C=	NP_066268.1:n.594-9C=
NM_138736.2:c.594-9C=	NP_620073.2:n.594-9C=
XM_011523003.1:c.468-9C=	XP_011521305.1:n.468-9C=
XM_011523003.3:c.468-9C=	XP_011521305.1:n.468-9C=
NM_020988.3:c.594-9C= MANE Select	NP_066268.1:n.594-9C=
NM_138736.3:c.594-9C=	NP_620073.2:n.594-9C=