Canonical Allele Identifier: CA395955397

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388940A>G (hg19) ; chr16:g.56355028A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56355028A>G , CM000678.2:g.56355028A>G	GRCh38
NC_000016.9:g.56388940A>G , CM000678.1:g.56388940A>G	GRCh37
NC_000016.8:g.54946441A>G	NCBI36
NG_042800.1:g.168690A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.1040A>G MANE Select	ENSP00000262493.6:p.Asn347Ser
ENST00000562316.6:c.545-1075A>G	ENSP00000457238.2:n.545-1075A>G
ENST00000564727.2:c.303+41A>G	ENSP00000454971.2:n.303+41A>G
ENST00000568375.2:c.278A>G
ENST00000638210.1:n.1340A>G
ENST00000638705.1:c.1040A>G	ENSP00000491223.1:p.Asn347Ser
ENST00000638836.1:n.950A>G
ENST00000639251.1:n.941A>G
ENST00000639268.1:c.675A>G
ENST00000639341.1:c.565A>G
ENST00000639770.1:c.1078A>G	ENSP00000491999.1:n.1078A>G
ENST00000640390.1:n.970A>G
ENST00000640469.1:c.404A>G	ENSP00000491875.1:p.Asn135Ser
ENST00000640560.1:n.816A>G
ENST00000640893.1:c.*438A>G	ENSP00000492677.1:n.*438A>G
ENST00000262493.10:c.1040A>G	ENSP00000262493.6:p.Asn347Ser
ENST00000564727.1:c.260A>G	ENSP00000454971.1:p.Asn87Ser
ENST00000568375.1:n.278A>G
NM_020988.2:c.1040A>G	NP_066268.1:p.Asn347Ser
XM_011523003.1:c.914A>G	XP_011521305.1:p.Asn305Ser
XM_011523003.3:c.914A>G	XP_011521305.1:p.Asn305Ser
NM_020988.3:c.1040A>G MANE Select	NP_066268.1:p.Asn347Ser