Canonical Allele Identifier: CA2224101082

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334461C= , CM000678.2:g.56334461C=	GRCh38
NC_000016.9:g.56368373C= , CM000678.1:g.56368373C=	GRCh37
NC_000016.8:g.54925874C=	NCBI36
NG_042800.1:g.148123C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.465-268C=	ENSP00000262494.7:n.465-268C=
ENST00000262493.12:c.465-268C= MANE Select	ENSP00000262493.6:n.465-268C=
ENST00000262494.12:c.465-268C=	ENSP00000262494.7:n.465-268C=
ENST00000562316.6:c.132-268C=	ENSP00000457238.2:n.132-268C=
ENST00000638185.1:n.680-268C=
ENST00000638210.1:n.765-268C=
ENST00000638705.1:c.465-268C=	ENSP00000491223.1:n.465-268C=
ENST00000638836.1:n.375-268C=
ENST00000639055.1:n.1186-268C=
ENST00000639251.1:n.366-268C=
ENST00000639268.1:c.229-2270C=
ENST00000639770.1:c.503-268C=	ENSP00000491999.1:n.503-268C=
ENST00000640390.1:n.395-268C=
ENST00000640893.1:c.304-268C=	ENSP00000492677.1:n.304-268C=
ENST00000262493.10:c.465-268C=	ENSP00000262493.6:n.465-268C=
ENST00000262494.11:c.465-268C=	ENSP00000262494.7:n.465-268C=
ENST00000562316.5:c.204-268C=	ENSP00000457238.1:n.204-268C=
ENST00000563440.1:c.204-268C=	ENSP00000455774.1:n.204-268C=
ENST00000565363.5:c.339-268C=	ENSP00000454728.1:n.339-268C=
NM_020988.2:c.465-268C=	NP_066268.1:n.465-268C=
NM_138736.2:c.465-268C=	NP_620073.2:n.465-268C=
XM_011523003.1:c.339-268C=	XP_011521305.1:n.339-268C=
XM_011523003.3:c.339-268C=	XP_011521305.1:n.339-268C=
NM_020988.3:c.465-268C= MANE Select	NP_066268.1:n.465-268C=
NM_138736.3:c.465-268C=	NP_620073.2:n.465-268C=