Canonical Allele Identifier: CA395955440

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388953C>G (hg19) ; chr16:g.56355041C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56355041C>G , CM000678.2:g.56355041C>G	GRCh38
NC_000016.9:g.56388953C>G , CM000678.1:g.56388953C>G	GRCh37
NC_000016.8:g.54946454C>G	NCBI36
NG_042800.1:g.168703C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.1053C>G MANE Select	ENSP00000262493.6:p.Cys351Trp
ENST00000562316.6:c.545-1062C>G	ENSP00000457238.2:n.545-1062C>G
ENST00000564727.2:c.303+54C>G	ENSP00000454971.2:n.303+54C>G
ENST00000568375.2:c.291C>G
ENST00000638210.1:n.1353C>G
ENST00000638705.1:c.1053C>G	ENSP00000491223.1:p.Cys351Trp
ENST00000638836.1:n.963C>G
ENST00000639251.1:n.954C>G
ENST00000639268.1:c.688C>G
ENST00000639341.1:c.578C>G
ENST00000639770.1:c.1091C>G	ENSP00000491999.1:n.1091C>G
ENST00000640390.1:n.983C>G
ENST00000640469.1:c.417C>G	ENSP00000491875.1:p.Cys139Trp
ENST00000640560.1:n.829C>G
ENST00000640893.1:c.*451C>G	ENSP00000492677.1:n.*451C>G
ENST00000262493.10:c.1053C>G	ENSP00000262493.6:p.Cys351Trp
ENST00000564727.1:c.273C>G	ENSP00000454971.1:p.Cys91Trp
ENST00000568375.1:n.291C>G
NM_020988.2:c.1053C>G	NP_066268.1:p.Cys351Trp
XM_011523003.1:c.927C>G	XP_011521305.1:p.Cys309Trp
XM_011523003.3:c.927C>G	XP_011521305.1:p.Cys309Trp
NM_020988.3:c.1053C>G MANE Select	NP_066268.1:p.Cys351Trp