Canonical Allele Identifier: CA395955204

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388885A>G (hg19) ; chr16:g.56354973A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354973A>G , CM000678.2:g.56354973A>G	GRCh38
NC_000016.9:g.56388885A>G , CM000678.1:g.56388885A>G	GRCh37
NC_000016.8:g.54946386A>G	NCBI36
NG_042800.1:g.168635A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262493.12:c.985A>G MANE Select	ENSP00000262493.6:p.Thr329Ala
ENST00000562316.6:c.545-1130A>G	ENSP00000457238.2:n.545-1130A>G
ENST00000564727.2:c.289A>G	ENSP00000454971.2:p.Thr97Ala
ENST00000568375.2:c.223A>G
ENST00000638210.1:n.1285A>G
ENST00000638705.1:c.985A>G	ENSP00000491223.1:p.Thr329Ala
ENST00000638836.1:n.895A>G
ENST00000639251.1:n.886A>G
ENST00000639268.1:c.620A>G
ENST00000639341.1:c.510A>G
ENST00000639770.1:c.1023A>G	ENSP00000491999.1:n.1023A>G
ENST00000640390.1:n.915A>G
ENST00000640469.1:c.349A>G	ENSP00000491875.1:p.Thr117Ala
ENST00000640560.1:n.761A>G
ENST00000640893.1:c.*383A>G	ENSP00000492677.1:n.*383A>G
ENST00000262493.10:c.985A>G	ENSP00000262493.6:p.Thr329Ala
ENST00000564727.1:c.205A>G	ENSP00000454971.1:p.Thr69Ala
ENST00000568375.1:n.223A>G
NM_020988.2:c.985A>G	NP_066268.1:p.Thr329Ala
XM_011523003.1:c.859A>G	XP_011521305.1:p.Thr287Ala
XM_011523003.3:c.859A>G	XP_011521305.1:p.Thr287Ala
NM_020988.3:c.985A>G MANE Select	NP_066268.1:p.Thr329Ala