Canonical Allele Identifier: CA395954715

Gene: GNAO1

Linked Data

• gnomAD v4: 16-56351441-A-G
• MyVariant Identifiers: chr16:g.56385353A>G (hg19) ; chr16:g.56351441A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351441A>G , CM000678.2:g.56351441A>G	GRCh38
NC_000016.9:g.56385353A>G , CM000678.1:g.56385353A>G	GRCh37
NC_000016.8:g.54942854A>G	NCBI36
NG_042800.1:g.165103A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.781A>G MANE Select	ENSP00000262493.6:p.Ile261Val
ENST00000562316.6:c.448A>G	ENSP00000457238.2:p.Ile150Val
ENST00000564727.2:c.85A>G	ENSP00000454971.2:p.Ile29Val
ENST00000568375.2:c.116-3425A>G
ENST00000638185.1:n.996A>G
ENST00000638210.1:n.1081A>G
ENST00000638705.1:c.781A>G	ENSP00000491223.1:p.Ile261Val
ENST00000638836.1:n.691A>G
ENST00000639055.1:n.1502A>G
ENST00000639251.1:n.682A>G
ENST00000639268.1:c.416A>G
ENST00000639341.1:c.306A>G
ENST00000639770.1:c.819A>G	ENSP00000491999.1:n.819A>G
ENST00000640390.1:n.711A>G
ENST00000640469.1:c.145A>G	ENSP00000491875.1:p.Ile49Val
ENST00000640560.1:n.557A>G
ENST00000640893.1:c.*179A>G	ENSP00000492677.1:n.*179A>G
ENST00000262493.10:c.781A>G	ENSP00000262493.6:p.Ile261Val
ENST00000564727.1:c.1A>G	ENSP00000454971.1:p.Ile1Val
ENST00000568375.1:n.116-3425A>G
NM_020988.2:c.781A>G	NP_066268.1:p.Ile261Val
XM_011523003.1:c.655A>G	XP_011521305.1:p.Ile219Val
XM_011523003.3:c.655A>G	XP_011521305.1:p.Ile219Val
NM_020988.3:c.781A>G MANE Select	NP_066268.1:p.Ile261Val