Canonical Allele Identifier: CA495585957

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388872T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354960T>G , CM000678.2:g.56354960T>G	GRCh38
NC_000016.9:g.56388872T>G , CM000678.1:g.56388872T>G	GRCh37
NC_000016.8:g.54946373T>G	NCBI36
NG_042800.1:g.168622T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.972T>G MANE Select	ENSP00000262493.6:p.Thr324=
ENST00000562316.6:c.545-1143T>G	ENSP00000457238.2:n.545-1143T>G
ENST00000564727.2:c.276T>G	ENSP00000454971.2:p.Thr92=
ENST00000568375.2:c.210T>G
ENST00000638210.1:n.1272T>G
ENST00000638705.1:c.972T>G	ENSP00000491223.1:p.Thr324=
ENST00000638836.1:n.882T>G
ENST00000639251.1:n.873T>G
ENST00000639268.1:c.607T>G
ENST00000639341.1:c.497T>G
ENST00000639770.1:c.1010T>G	ENSP00000491999.1:n.1010T>G
ENST00000640390.1:n.902T>G
ENST00000640469.1:c.336T>G	ENSP00000491875.1:p.Thr112=
ENST00000640560.1:n.748T>G
ENST00000640893.1:c.*370T>G	ENSP00000492677.1:n.*370T>G
ENST00000262493.10:c.972T>G	ENSP00000262493.6:p.Thr324=
ENST00000564727.1:c.192T>G	ENSP00000454971.1:p.Thr64=
ENST00000568375.1:n.210T>G
NM_020988.2:c.972T>G	NP_066268.1:p.Thr324=
XM_011523003.1:c.846T>G	XP_011521305.1:p.Thr282=
XM_011523003.3:c.846T>G	XP_011521305.1:p.Thr282=
NM_020988.3:c.972T>G MANE Select	NP_066268.1:p.Thr324=