Canonical Allele Identifier: CA395954822

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385398G>C (hg19) ; chr16:g.56351486G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351486G>C , CM000678.2:g.56351486G>C	GRCh38
NC_000016.9:g.56385398G>C , CM000678.1:g.56385398G>C	GRCh37
NC_000016.8:g.54942899G>C	NCBI36
NG_042800.1:g.165148G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.826G>C MANE Select	ENSP00000262493.6:p.Gly276Arg
ENST00000562316.6:c.493G>C	ENSP00000457238.2:p.Gly165Arg
ENST00000564727.2:c.130G>C	ENSP00000454971.2:p.Gly44Arg
ENST00000568375.2:c.116-3380G>C
ENST00000638185.1:n.1041G>C
ENST00000638210.1:n.1126G>C
ENST00000638705.1:c.826G>C	ENSP00000491223.1:p.Gly276Arg
ENST00000638836.1:n.736G>C
ENST00000639055.1:n.1547G>C
ENST00000639251.1:n.727G>C
ENST00000639268.1:c.461G>C
ENST00000639341.1:c.351G>C
ENST00000639770.1:c.864G>C	ENSP00000491999.1:n.864G>C
ENST00000640390.1:n.756G>C
ENST00000640469.1:c.190G>C	ENSP00000491875.1:p.Gly64Arg
ENST00000640560.1:n.602G>C
ENST00000640893.1:c.*224G>C	ENSP00000492677.1:n.*224G>C
ENST00000262493.10:c.826G>C	ENSP00000262493.6:p.Gly276Arg
ENST00000564727.1:c.46G>C	ENSP00000454971.1:p.Gly16Arg
ENST00000568375.1:n.116-3380G>C
NM_020988.2:c.826G>C	NP_066268.1:p.Gly276Arg
XM_011523003.1:c.700G>C	XP_011521305.1:p.Gly234Arg
XM_011523003.3:c.700G>C	XP_011521305.1:p.Gly234Arg
NM_020988.3:c.826G>C MANE Select	NP_066268.1:p.Gly276Arg