Canonical Allele Identifier: CA395952392

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370757C>A (hg19) ; chr16:g.56336845C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336845C>A , CM000678.2:g.56336845C>A	GRCh38
NC_000016.9:g.56370757C>A , CM000678.1:g.56370757C>A	GRCh37
NC_000016.8:g.54928258C>A	NCBI36
NG_042800.1:g.150507C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262494.13:c.708C>A	ENSP00000262494.7:p.His236Gln
ENST00000262493.12:c.708C>A MANE Select	ENSP00000262493.6:p.His236Gln
ENST00000262494.12:c.708C>A	ENSP00000262494.7:p.His236Gln
ENST00000562316.6:c.375C>A	ENSP00000457238.2:p.His125Gln
ENST00000564727.2:c.12C>A	ENSP00000454971.2:p.His4Gln
ENST00000568375.2:c.100C>A
ENST00000638185.1:n.923C>A
ENST00000638210.1:n.1008C>A
ENST00000638705.1:c.708C>A	ENSP00000491223.1:p.His236Gln
ENST00000638836.1:n.618C>A
ENST00000639055.1:n.1429C>A
ENST00000639251.1:n.609C>A
ENST00000639268.1:c.343C>A
ENST00000639341.1:c.233C>A
ENST00000639770.1:c.746C>A	ENSP00000491999.1:n.746C>A
ENST00000640390.1:n.638C>A
ENST00000640469.1:c.72C>A	ENSP00000491875.1:p.His24Gln
ENST00000640560.1:n.484C>A
ENST00000640893.1:c.*106C>A	ENSP00000492677.1:n.*106C>A
ENST00000262493.10:c.708C>A	ENSP00000262493.6:p.His236Gln
ENST00000262494.11:c.708C>A	ENSP00000262494.7:p.His236Gln
ENST00000568375.1:n.100C>A
NM_020988.2:c.708C>A	NP_066268.1:p.His236Gln
NM_138736.2:c.708C>A	NP_620073.2:p.His236Gln
XM_011523003.1:c.582C>A	XP_011521305.1:p.His194Gln
XM_011523003.3:c.582C>A	XP_011521305.1:p.His194Gln
NM_020988.3:c.708C>A MANE Select	NP_066268.1:p.His236Gln
NM_138736.3:c.708C>A	NP_620073.2:p.His236Gln