Canonical Allele Identifier: CA395954726

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385357A>G (hg19) ; chr16:g.56351445A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351445A>G , CM000678.2:g.56351445A>G	GRCh38
NC_000016.9:g.56385357A>G , CM000678.1:g.56385357A>G	GRCh37
NC_000016.8:g.54942858A>G	NCBI36
NG_042800.1:g.165107A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.785A>G MANE Select	ENSP00000262493.6:p.Asp262Gly
ENST00000562316.6:c.452A>G	ENSP00000457238.2:p.Asp151Gly
ENST00000564727.2:c.89A>G	ENSP00000454971.2:p.Asp30Gly
ENST00000568375.2:c.116-3421A>G
ENST00000638185.1:n.1000A>G
ENST00000638210.1:n.1085A>G
ENST00000638705.1:c.785A>G	ENSP00000491223.1:p.Asp262Gly
ENST00000638836.1:n.695A>G
ENST00000639055.1:n.1506A>G
ENST00000639251.1:n.686A>G
ENST00000639268.1:c.420A>G
ENST00000639341.1:c.310A>G
ENST00000639770.1:c.823A>G	ENSP00000491999.1:n.823A>G
ENST00000640390.1:n.715A>G
ENST00000640469.1:c.149A>G	ENSP00000491875.1:p.Asp50Gly
ENST00000640560.1:n.561A>G
ENST00000640893.1:c.*183A>G	ENSP00000492677.1:n.*183A>G
ENST00000262493.10:c.785A>G	ENSP00000262493.6:p.Asp262Gly
ENST00000564727.1:c.5A>G	ENSP00000454971.1:p.Asp2Gly
ENST00000568375.1:n.116-3421A>G
NM_020988.2:c.785A>G	NP_066268.1:p.Asp262Gly
XM_011523003.1:c.659A>G	XP_011521305.1:p.Asp220Gly
XM_011523003.3:c.659A>G	XP_011521305.1:p.Asp220Gly
NM_020988.3:c.785A>G MANE Select	NP_066268.1:p.Asp262Gly