Canonical Allele Identifier: CA395952173

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370662C>G (hg19) ; chr16:g.56336750C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336750C>G , CM000678.2:g.56336750C>G	GRCh38
NC_000016.9:g.56370662C>G , CM000678.1:g.56370662C>G	GRCh37
NC_000016.8:g.54928163C>G	NCBI36
NG_042800.1:g.150412C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.613C>G	ENSP00000262494.7:p.Gln205Glu
ENST00000262493.12:c.613C>G MANE Select	ENSP00000262493.6:p.Gln205Glu
ENST00000262494.12:c.613C>G	ENSP00000262494.7:p.Gln205Glu
ENST00000562316.6:c.280C>G	ENSP00000457238.2:p.Gln94Glu
ENST00000568375.2:c.5C>G
ENST00000638185.1:n.828C>G
ENST00000638210.1:n.913C>G
ENST00000638705.1:c.613C>G	ENSP00000491223.1:p.Gln205Glu
ENST00000638836.1:n.523C>G
ENST00000639055.1:n.1334C>G
ENST00000639251.1:n.514C>G
ENST00000639268.1:c.248C>G
ENST00000639341.1:c.138C>G
ENST00000639770.1:c.651C>G	ENSP00000491999.1:n.651C>G
ENST00000640390.1:n.543C>G
ENST00000640560.1:n.389C>G
ENST00000640893.1:c.*11C>G	ENSP00000492677.1:n.*11C>G
ENST00000262493.10:c.613C>G	ENSP00000262493.6:p.Gln205Glu
ENST00000262494.11:c.613C>G	ENSP00000262494.7:p.Gln205Glu
ENST00000568375.1:n.5C>G
NM_020988.2:c.613C>G	NP_066268.1:p.Gln205Glu
NM_138736.2:c.613C>G	NP_620073.2:p.Gln205Glu
XM_011523003.1:c.487C>G	XP_011521305.1:p.Gln163Glu
XM_011523003.3:c.487C>G	XP_011521305.1:p.Gln163Glu
NM_020988.3:c.613C>G MANE Select	NP_066268.1:p.Gln205Glu
NM_138736.3:c.613C>G	NP_620073.2:p.Gln205Glu