Canonical Allele Identifier: CA395954832

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385403G>C (hg19) ; chr16:g.56351491G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351491G>C , CM000678.2:g.56351491G>C	GRCh38
NC_000016.9:g.56385403G>C , CM000678.1:g.56385403G>C	GRCh37
NC_000016.8:g.54942904G>C	NCBI36
NG_042800.1:g.165153G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.831G>C MANE Select	ENSP00000262493.6:p.Glu277Asp
ENST00000562316.6:c.498G>C	ENSP00000457238.2:p.Glu166Asp
ENST00000564727.2:c.135G>C	ENSP00000454971.2:p.Glu45Asp
ENST00000568375.2:c.116-3375G>C
ENST00000638185.1:n.1046G>C
ENST00000638210.1:n.1131G>C
ENST00000638705.1:c.831G>C	ENSP00000491223.1:p.Glu277Asp
ENST00000638836.1:n.741G>C
ENST00000639055.1:n.1552G>C
ENST00000639251.1:n.732G>C
ENST00000639268.1:c.466G>C
ENST00000639341.1:c.356G>C
ENST00000639770.1:c.869G>C	ENSP00000491999.1:n.869G>C
ENST00000640390.1:n.761G>C
ENST00000640469.1:c.195G>C	ENSP00000491875.1:p.Glu65Asp
ENST00000640560.1:n.607G>C
ENST00000640893.1:c.*229G>C	ENSP00000492677.1:n.*229G>C
ENST00000262493.10:c.831G>C	ENSP00000262493.6:p.Glu277Asp
ENST00000564727.1:c.51G>C	ENSP00000454971.1:p.Glu17Asp
ENST00000568375.1:n.116-3375G>C
NM_020988.2:c.831G>C	NP_066268.1:p.Glu277Asp
XM_011523003.1:c.705G>C	XP_011521305.1:p.Glu235Asp
XM_011523003.3:c.705G>C	XP_011521305.1:p.Glu235Asp
NM_020988.3:c.831G>C MANE Select	NP_066268.1:p.Glu277Asp