Canonical Allele Identifier: CA395952269

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56370702A>C (hg19) ; chr16:g.56336790A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336790A>C , CM000678.2:g.56336790A>C	GRCh38
NC_000016.9:g.56370702A>C , CM000678.1:g.56370702A>C	GRCh37
NC_000016.8:g.54928203A>C	NCBI36
NG_042800.1:g.150452A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.653A>C	ENSP00000262494.7:p.Asp218Ala
ENST00000262493.12:c.653A>C MANE Select	ENSP00000262493.6:p.Asp218Ala
ENST00000262494.12:c.653A>C	ENSP00000262494.7:p.Asp218Ala
ENST00000562316.6:c.320A>C	ENSP00000457238.2:p.Asp107Ala
ENST00000568375.2:c.45A>C
ENST00000638185.1:n.868A>C
ENST00000638210.1:n.953A>C
ENST00000638705.1:c.653A>C	ENSP00000491223.1:p.Asp218Ala
ENST00000638836.1:n.563A>C
ENST00000639055.1:n.1374A>C
ENST00000639251.1:n.554A>C
ENST00000639268.1:c.288A>C
ENST00000639341.1:c.178A>C
ENST00000639770.1:c.691A>C	ENSP00000491999.1:n.691A>C
ENST00000640390.1:n.583A>C
ENST00000640469.1:c.17A>C	ENSP00000491875.1:p.Asp6Ala
ENST00000640560.1:n.429A>C
ENST00000640893.1:c.*51A>C	ENSP00000492677.1:n.*51A>C
ENST00000262493.10:c.653A>C	ENSP00000262493.6:p.Asp218Ala
ENST00000262494.11:c.653A>C	ENSP00000262494.7:p.Asp218Ala
ENST00000568375.1:n.45A>C
NM_020988.2:c.653A>C	NP_066268.1:p.Asp218Ala
NM_138736.2:c.653A>C	NP_620073.2:p.Asp218Ala
XM_011523003.1:c.527A>C	XP_011521305.1:p.Asp176Ala
XM_011523003.3:c.527A>C	XP_011521305.1:p.Asp176Ala
NM_020988.3:c.653A>C MANE Select	NP_066268.1:p.Asp218Ala
NM_138736.3:c.653A>C	NP_620073.2:p.Asp218Ala