Canonical Allele Identifier: CA395954896

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385431T>G (hg19) ; chr16:g.56351519T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351519T>G , CM000678.2:g.56351519T>G	GRCh38
NC_000016.9:g.56385431T>G , CM000678.1:g.56385431T>G	GRCh37
NC_000016.8:g.54942932T>G	NCBI36
NG_042800.1:g.165181T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.859T>G MANE Select	ENSP00000262493.6:p.Cys287Gly
ENST00000562316.6:c.526T>G	ENSP00000457238.2:p.Cys176Gly
ENST00000564727.2:c.163T>G	ENSP00000454971.2:p.Cys55Gly
ENST00000568375.2:c.116-3347T>G
ENST00000638185.1:n.1074T>G
ENST00000638210.1:n.1159T>G
ENST00000638705.1:c.859T>G	ENSP00000491223.1:p.Cys287Gly
ENST00000638836.1:n.769T>G
ENST00000639055.1:n.1580T>G
ENST00000639251.1:n.760T>G
ENST00000639268.1:c.494T>G
ENST00000639341.1:c.384T>G
ENST00000639770.1:c.897T>G	ENSP00000491999.1:n.897T>G
ENST00000640390.1:n.789T>G
ENST00000640469.1:c.223T>G	ENSP00000491875.1:p.Cys75Gly
ENST00000640560.1:n.635T>G
ENST00000640893.1:c.*257T>G	ENSP00000492677.1:n.*257T>G
ENST00000262493.10:c.859T>G	ENSP00000262493.6:p.Cys287Gly
ENST00000564727.1:c.79T>G	ENSP00000454971.1:p.Cys27Gly
ENST00000568375.1:n.116-3347T>G
NM_020988.2:c.859T>G	NP_066268.1:p.Cys287Gly
XM_011523003.1:c.733T>G	XP_011521305.1:p.Cys245Gly
XM_011523003.3:c.733T>G	XP_011521305.1:p.Cys245Gly
NM_020988.3:c.859T>G MANE Select	NP_066268.1:p.Cys287Gly