Canonical Allele Identifier: CA395954675

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385338A>G (hg19) ; chr16:g.56351426A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351426A>G , CM000678.2:g.56351426A>G	GRCh38
NC_000016.9:g.56385338A>G , CM000678.1:g.56385338A>G	GRCh37
NC_000016.8:g.54942839A>G	NCBI36
NG_042800.1:g.165088A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.766A>G MANE Select	ENSP00000262493.6:p.Asn256Asp
ENST00000562316.6:c.433A>G	ENSP00000457238.2:p.Asn145Asp
ENST00000564727.2:c.70A>G	ENSP00000454971.2:p.Asn24Asp
ENST00000568375.2:c.116-3440A>G
ENST00000638185.1:n.981A>G
ENST00000638210.1:n.1066A>G
ENST00000638705.1:c.766A>G	ENSP00000491223.1:p.Asn256Asp
ENST00000638836.1:n.676A>G
ENST00000639055.1:n.1487A>G
ENST00000639251.1:n.667A>G
ENST00000639268.1:c.401A>G
ENST00000639341.1:c.291A>G
ENST00000639770.1:c.804A>G	ENSP00000491999.1:n.804A>G
ENST00000640390.1:n.696A>G
ENST00000640469.1:c.130A>G	ENSP00000491875.1:p.Asn44Asp
ENST00000640560.1:n.542A>G
ENST00000640893.1:c.*164A>G	ENSP00000492677.1:n.*164A>G
ENST00000262493.10:c.766A>G	ENSP00000262493.6:p.Asn256Asp
ENST00000568375.1:n.116-3440A>G
NM_020988.2:c.766A>G	NP_066268.1:p.Asn256Asp
XM_011523003.1:c.640A>G	XP_011521305.1:p.Asn214Asp
XM_011523003.3:c.640A>G	XP_011521305.1:p.Asn214Asp
NM_020988.3:c.766A>G MANE Select	NP_066268.1:p.Asn256Asp