Canonical Allele Identifier: CA395951677

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56368738A>G (hg19) ; chr16:g.56334826A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334826A>G , CM000678.2:g.56334826A>G	GRCh38
NC_000016.9:g.56368738A>G , CM000678.1:g.56368738A>G	GRCh37
NC_000016.8:g.54926239A>G	NCBI36
NG_042800.1:g.148488A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.562A>G	ENSP00000262494.7:p.Thr188Ala
ENST00000262493.12:c.562A>G MANE Select	ENSP00000262493.6:p.Thr188Ala
ENST00000262494.12:c.562A>G	ENSP00000262494.7:p.Thr188Ala
ENST00000562316.6:c.229A>G	ENSP00000457238.2:p.Thr77Ala
ENST00000638185.1:n.777A>G
ENST00000638210.1:n.862A>G
ENST00000638705.1:c.562A>G	ENSP00000491223.1:p.Thr188Ala
ENST00000638836.1:n.472A>G
ENST00000639055.1:n.1283A>G
ENST00000639251.1:n.463A>G
ENST00000639268.1:c.229-1905A>G
ENST00000639341.1:c.87A>G
ENST00000639770.1:c.600A>G	ENSP00000491999.1:n.600A>G
ENST00000640390.1:n.492A>G
ENST00000640893.1:c.401A>G	ENSP00000492677.1:p.Asn134Ser
ENST00000262493.10:c.562A>G	ENSP00000262493.6:p.Thr188Ala
ENST00000262494.11:c.562A>G	ENSP00000262494.7:p.Thr188Ala
ENST00000562316.5:c.301A>G	ENSP00000457238.1:p.Thr101Ala
NM_020988.2:c.562A>G	NP_066268.1:p.Thr188Ala
NM_138736.2:c.562A>G	NP_620073.2:p.Thr188Ala
XM_011523003.1:c.436A>G	XP_011521305.1:p.Thr146Ala
XM_011523003.3:c.436A>G	XP_011521305.1:p.Thr146Ala
NM_020988.3:c.562A>G MANE Select	NP_066268.1:p.Thr188Ala
NM_138736.3:c.562A>G	NP_620073.2:p.Thr188Ala