Canonical Allele Identifier: CA2224101079

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334457T= , CM000678.2:g.56334457T=	GRCh38
NC_000016.9:g.56368369T= , CM000678.1:g.56368369T=	GRCh37
NC_000016.8:g.54925870T=	NCBI36
NG_042800.1:g.148119T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.465-272T=	ENSP00000262494.7:n.465-272T=
ENST00000262493.12:c.465-272T= MANE Select	ENSP00000262493.6:n.465-272T=
ENST00000262494.12:c.465-272T=	ENSP00000262494.7:n.465-272T=
ENST00000562316.6:c.132-272T=	ENSP00000457238.2:n.132-272T=
ENST00000638185.1:n.680-272T=
ENST00000638210.1:n.765-272T=
ENST00000638705.1:c.465-272T=	ENSP00000491223.1:n.465-272T=
ENST00000638836.1:n.375-272T=
ENST00000639055.1:n.1186-272T=
ENST00000639251.1:n.366-272T=
ENST00000639268.1:c.229-2274T=
ENST00000639770.1:c.503-272T=	ENSP00000491999.1:n.503-272T=
ENST00000640390.1:n.395-272T=
ENST00000640893.1:c.304-272T=	ENSP00000492677.1:n.304-272T=
ENST00000262493.10:c.465-272T=	ENSP00000262493.6:n.465-272T=
ENST00000262494.11:c.465-272T=	ENSP00000262494.7:n.465-272T=
ENST00000562316.5:c.204-272T=	ENSP00000457238.1:n.204-272T=
ENST00000563440.1:c.204-272T=	ENSP00000455774.1:n.204-272T=
ENST00000565363.5:c.339-272T=	ENSP00000454728.1:n.339-272T=
NM_020988.2:c.465-272T=	NP_066268.1:n.465-272T=
NM_138736.2:c.465-272T=	NP_620073.2:n.465-272T=
XM_011523003.1:c.339-272T=	XP_011521305.1:n.339-272T=
XM_011523003.3:c.339-272T=	XP_011521305.1:n.339-272T=
NM_020988.3:c.465-272T= MANE Select	NP_066268.1:n.465-272T=
NM_138736.3:c.465-272T=	NP_620073.2:n.465-272T=