Canonical Allele Identifier: CA395954672

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385337T>A (hg19) ; chr16:g.56351425T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351425T>A , CM000678.2:g.56351425T>A	GRCh38
NC_000016.9:g.56385337T>A , CM000678.1:g.56385337T>A	GRCh37
NC_000016.8:g.54942838T>A	NCBI36
NG_042800.1:g.165087T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.765T>A MANE Select	ENSP00000262493.6:p.Cys255Ter
ENST00000562316.6:c.432T>A	ENSP00000457238.2:p.Cys144Ter
ENST00000564727.2:c.69T>A	ENSP00000454971.2:p.Cys23Ter
ENST00000568375.2:c.116-3441T>A
ENST00000638185.1:n.980T>A
ENST00000638210.1:n.1065T>A
ENST00000638705.1:c.765T>A	ENSP00000491223.1:p.Cys255Ter
ENST00000638836.1:n.675T>A
ENST00000639055.1:n.1486T>A
ENST00000639251.1:n.666T>A
ENST00000639268.1:c.400T>A
ENST00000639341.1:c.290T>A
ENST00000639770.1:c.803T>A	ENSP00000491999.1:n.803T>A
ENST00000640390.1:n.695T>A
ENST00000640469.1:c.129T>A	ENSP00000491875.1:p.Cys43Ter
ENST00000640560.1:n.541T>A
ENST00000640893.1:c.*163T>A	ENSP00000492677.1:n.*163T>A
ENST00000262493.10:c.765T>A	ENSP00000262493.6:p.Cys255Ter
ENST00000568375.1:n.116-3441T>A
NM_020988.2:c.765T>A	NP_066268.1:p.Cys255Ter
XM_011523003.1:c.639T>A	XP_011521305.1:p.Cys213Ter
XM_011523003.3:c.639T>A	XP_011521305.1:p.Cys213Ter
NM_020988.3:c.765T>A MANE Select	NP_066268.1:p.Cys255Ter