Canonical Allele Identifier: CA2633314432

Gene: GNAO1

Linked Data

• gnomAD v4: 16-56334612-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334612C>A , CM000678.2:g.56334612C>A	GRCh38
NC_000016.9:g.56368524C>A , CM000678.1:g.56368524C>A	GRCh37
NC_000016.8:g.54926025C>A	NCBI36
NG_042800.1:g.148274C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.465-117C>A	ENSP00000262494.7:n.465-117C>A
ENST00000262493.12:c.465-117C>A MANE Select	ENSP00000262493.6:n.465-117C>A
ENST00000262494.12:c.465-117C>A	ENSP00000262494.7:n.465-117C>A
ENST00000562316.6:c.132-117C>A	ENSP00000457238.2:n.132-117C>A
ENST00000638185.1:n.680-117C>A
ENST00000638210.1:n.765-117C>A
ENST00000638705.1:c.465-117C>A	ENSP00000491223.1:n.465-117C>A
ENST00000638836.1:n.375-117C>A
ENST00000639055.1:n.1186-117C>A
ENST00000639251.1:n.366-117C>A
ENST00000639268.1:c.229-2119C>A
ENST00000639770.1:c.503-117C>A	ENSP00000491999.1:n.503-117C>A
ENST00000640390.1:n.395-117C>A
ENST00000640893.1:c.304-117C>A	ENSP00000492677.1:n.304-117C>A
ENST00000262493.10:c.465-117C>A	ENSP00000262493.6:n.465-117C>A
ENST00000262494.11:c.465-117C>A	ENSP00000262494.7:n.465-117C>A
ENST00000562316.5:c.204-117C>A	ENSP00000457238.1:n.204-117C>A
ENST00000563440.1:c.204-117C>A	ENSP00000455774.1:n.204-117C>A
ENST00000565363.5:c.339-117C>A	ENSP00000454728.1:n.339-117C>A
NM_020988.2:c.465-117C>A	NP_066268.1:n.465-117C>A
NM_138736.2:c.465-117C>A	NP_620073.2:n.465-117C>A
XM_011523003.1:c.339-117C>A	XP_011521305.1:n.339-117C>A
XM_011523003.3:c.339-117C>A	XP_011521305.1:n.339-117C>A
NM_020988.3:c.465-117C>A MANE Select	NP_066268.1:n.465-117C>A
NM_138736.3:c.465-117C>A	NP_620073.2:n.465-117C>A