Canonical Allele Identifier: CA495586057

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388956C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56355044C>T , CM000678.2:g.56355044C>T	GRCh38
NC_000016.9:g.56388956C>T , CM000678.1:g.56388956C>T	GRCh37
NC_000016.8:g.54946457C>T	NCBI36
NG_042800.1:g.168706C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.1056C>T MANE Select	ENSP00000262493.6:p.Gly352=
ENST00000562316.6:c.545-1059C>T	ENSP00000457238.2:n.545-1059C>T
ENST00000564727.2:c.303+57C>T	ENSP00000454971.2:n.303+57C>T
ENST00000568375.2:c.294C>T
ENST00000638210.1:n.1356C>T
ENST00000638705.1:c.1056C>T	ENSP00000491223.1:p.Gly352=
ENST00000638836.1:n.966C>T
ENST00000639251.1:n.957C>T
ENST00000639268.1:c.691C>T
ENST00000639341.1:c.581C>T
ENST00000639770.1:c.1094C>T	ENSP00000491999.1:n.1094C>T
ENST00000640390.1:n.986C>T
ENST00000640469.1:c.420C>T	ENSP00000491875.1:p.Gly140=
ENST00000640560.1:n.832C>T
ENST00000640893.1:c.*454C>T	ENSP00000492677.1:n.*454C>T
ENST00000262493.10:c.1056C>T	ENSP00000262493.6:p.Gly352=
ENST00000564727.1:c.276C>T	ENSP00000454971.1:p.Gly92=
ENST00000568375.1:n.294C>T
NM_020988.2:c.1056C>T	NP_066268.1:p.Gly352=
XM_011523003.1:c.930C>T	XP_011521305.1:p.Gly310=
XM_011523003.3:c.930C>T	XP_011521305.1:p.Gly310=
NM_020988.3:c.1056C>T MANE Select	NP_066268.1:p.Gly352=