Canonical Allele Identifier: CA395955211

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388888A>T (hg19) ; chr16:g.56354976A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354976A>T , CM000678.2:g.56354976A>T	GRCh38
NC_000016.9:g.56388888A>T , CM000678.1:g.56388888A>T	GRCh37
NC_000016.8:g.54946389A>T	NCBI36
NG_042800.1:g.168638A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.988A>T MANE Select	ENSP00000262493.6:p.Asn330Tyr
ENST00000562316.6:c.545-1127A>T	ENSP00000457238.2:n.545-1127A>T
ENST00000564727.2:c.292A>T	ENSP00000454971.2:p.Asn98Tyr
ENST00000568375.2:c.226A>T
ENST00000638210.1:n.1288A>T
ENST00000638705.1:c.988A>T	ENSP00000491223.1:p.Asn330Tyr
ENST00000638836.1:n.898A>T
ENST00000639251.1:n.889A>T
ENST00000639268.1:c.623A>T
ENST00000639341.1:c.513A>T
ENST00000639770.1:c.1026A>T	ENSP00000491999.1:n.1026A>T
ENST00000640390.1:n.918A>T
ENST00000640469.1:c.352A>T	ENSP00000491875.1:p.Asn118Tyr
ENST00000640560.1:n.764A>T
ENST00000640893.1:c.*386A>T	ENSP00000492677.1:n.*386A>T
ENST00000262493.10:c.988A>T	ENSP00000262493.6:p.Asn330Tyr
ENST00000564727.1:c.208A>T	ENSP00000454971.1:p.Asn70Tyr
ENST00000568375.1:n.226A>T
NM_020988.2:c.988A>T	NP_066268.1:p.Asn330Tyr
XM_011523003.1:c.862A>T	XP_011521305.1:p.Asn288Tyr
XM_011523003.3:c.862A>T	XP_011521305.1:p.Asn288Tyr
NM_020988.3:c.988A>T MANE Select	NP_066268.1:p.Asn330Tyr