Canonical Allele Identifier: CA395951611

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56368723A>G (hg19) ; chr16:g.56334811A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334811A>G , CM000678.2:g.56334811A>G	GRCh38
NC_000016.9:g.56368723A>G , CM000678.1:g.56368723A>G	GRCh37
NC_000016.8:g.54926224A>G	NCBI36
NG_042800.1:g.148473A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.547A>G	ENSP00000262494.7:p.Thr183Ala
ENST00000262493.12:c.547A>G MANE Select	ENSP00000262493.6:p.Thr183Ala
ENST00000262494.12:c.547A>G	ENSP00000262494.7:p.Thr183Ala
ENST00000562316.6:c.214A>G	ENSP00000457238.2:p.Thr72Ala
ENST00000638185.1:n.762A>G
ENST00000638210.1:n.847A>G
ENST00000638705.1:c.547A>G	ENSP00000491223.1:p.Thr183Ala
ENST00000638836.1:n.457A>G
ENST00000639055.1:n.1268A>G
ENST00000639251.1:n.448A>G
ENST00000639268.1:c.229-1920A>G
ENST00000639341.1:c.72A>G
ENST00000639770.1:c.585A>G	ENSP00000491999.1:n.585A>G
ENST00000640390.1:n.477A>G
ENST00000640893.1:c.386A>G	ENSP00000492677.1:p.His129Arg
ENST00000262493.10:c.547A>G	ENSP00000262493.6:p.Thr183Ala
ENST00000262494.11:c.547A>G	ENSP00000262494.7:p.Thr183Ala
ENST00000562316.5:c.286A>G	ENSP00000457238.1:p.Thr96Ala
NM_020988.2:c.547A>G	NP_066268.1:p.Thr183Ala
NM_138736.2:c.547A>G	NP_620073.2:p.Thr183Ala
XM_011523003.1:c.421A>G	XP_011521305.1:p.Thr141Ala
XM_011523003.3:c.421A>G	XP_011521305.1:p.Thr141Ala
NM_020988.3:c.547A>G MANE Select	NP_066268.1:p.Thr183Ala
NM_138736.3:c.547A>G	NP_620073.2:p.Thr183Ala