Canonical Allele Identifier: CA2633321922

Gene: GNAO1

Linked Data

• gnomAD v4: 16-56351488-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351488C>A , CM000678.2:g.56351488C>A	GRCh38
NC_000016.9:g.56385400C>A , CM000678.1:g.56385400C>A	GRCh37
NC_000016.8:g.54942901C>A	NCBI36
NG_042800.1:g.165150C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.828C>A MANE Select	ENSP00000262493.6:p.Gly276=
ENST00000562316.6:c.495C>A	ENSP00000457238.2:p.Gly165=
ENST00000564727.2:c.132C>A	ENSP00000454971.2:p.Gly44=
ENST00000568375.2:c.116-3378C>A
ENST00000638185.1:n.1043C>A
ENST00000638210.1:n.1128C>A
ENST00000638705.1:c.828C>A	ENSP00000491223.1:p.Gly276=
ENST00000638836.1:n.738C>A
ENST00000639055.1:n.1549C>A
ENST00000639251.1:n.729C>A
ENST00000639268.1:c.463C>A
ENST00000639341.1:c.353C>A
ENST00000639770.1:c.866C>A	ENSP00000491999.1:n.866C>A
ENST00000640390.1:n.758C>A
ENST00000640469.1:c.192C>A	ENSP00000491875.1:p.Gly64=
ENST00000640560.1:n.604C>A
ENST00000640893.1:c.*226C>A	ENSP00000492677.1:n.*226C>A
ENST00000262493.10:c.828C>A	ENSP00000262493.6:p.Gly276=
ENST00000564727.1:c.48C>A	ENSP00000454971.1:p.Gly16=
ENST00000568375.1:n.116-3378C>A
NM_020988.2:c.828C>A	NP_066268.1:p.Gly276=
XM_011523003.1:c.702C>A	XP_011521305.1:p.Gly234=
XM_011523003.3:c.702C>A	XP_011521305.1:p.Gly234=
NM_020988.3:c.828C>A MANE Select	NP_066268.1:p.Gly276=