Canonical Allele Identifier: CA395951373

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56368642T>G (hg19) ; chr16:g.56334730T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334730T>G , CM000678.2:g.56334730T>G	GRCh38
NC_000016.9:g.56368642T>G , CM000678.1:g.56368642T>G	GRCh37
NC_000016.8:g.54926143T>G	NCBI36
NG_042800.1:g.148392T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262494.13:c.466T>G	ENSP00000262494.7:p.Tyr156Asp
ENST00000262493.12:c.466T>G MANE Select	ENSP00000262493.6:p.Tyr156Asp
ENST00000262494.12:c.466T>G	ENSP00000262494.7:p.Tyr156Asp
ENST00000562316.6:c.133T>G	ENSP00000457238.2:p.Tyr45Asp
ENST00000638185.1:n.681T>G
ENST00000638210.1:n.766T>G
ENST00000638705.1:c.466T>G	ENSP00000491223.1:p.Tyr156Asp
ENST00000638836.1:n.376T>G
ENST00000639055.1:n.1187T>G
ENST00000639251.1:n.367T>G
ENST00000639268.1:c.229-2001T>G
ENST00000639770.1:c.504T>G	ENSP00000491999.1:n.504T>G
ENST00000640390.1:n.396T>G
ENST00000640893.1:c.305T>G	ENSP00000492677.1:p.Leu102Arg
ENST00000262493.10:c.466T>G	ENSP00000262493.6:p.Tyr156Asp
ENST00000262494.11:c.466T>G	ENSP00000262494.7:p.Tyr156Asp
ENST00000562316.5:c.205T>G	ENSP00000457238.1:p.Tyr69Asp
ENST00000563440.1:c.205T>G	ENSP00000455774.1:p.Tyr69Asp
ENST00000565363.5:c.340T>G	ENSP00000454728.1:p.Tyr114Asp
NM_020988.2:c.466T>G	NP_066268.1:p.Tyr156Asp
NM_138736.2:c.466T>G	NP_620073.2:p.Tyr156Asp
XM_011523003.1:c.340T>G	XP_011521305.1:p.Tyr114Asp
XM_011523003.3:c.340T>G	XP_011521305.1:p.Tyr114Asp
NM_020988.3:c.466T>G MANE Select	NP_066268.1:p.Tyr156Asp
NM_138736.3:c.466T>G	NP_620073.2:p.Tyr156Asp