Canonical Allele Identifier: CA395954634

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385321T>G (hg19) ; chr16:g.56351409T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351409T>G , CM000678.2:g.56351409T>G	GRCh38
NC_000016.9:g.56385321T>G , CM000678.1:g.56385321T>G	GRCh37
NC_000016.8:g.54942822T>G	NCBI36
NG_042800.1:g.165071T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262493.12:c.749T>G MANE Select	ENSP00000262493.6:p.Leu250Arg
ENST00000562316.6:c.416T>G	ENSP00000457238.2:p.Leu139Arg
ENST00000564727.2:c.53T>G	ENSP00000454971.2:p.Leu18Arg
ENST00000568375.2:c.116-3457T>G
ENST00000638185.1:n.964T>G
ENST00000638210.1:n.1049T>G
ENST00000638705.1:c.749T>G	ENSP00000491223.1:p.Leu250Arg
ENST00000638836.1:n.659T>G
ENST00000639055.1:n.1470T>G
ENST00000639251.1:n.650T>G
ENST00000639268.1:c.384T>G
ENST00000639341.1:c.274T>G
ENST00000639770.1:c.787T>G	ENSP00000491999.1:n.787T>G
ENST00000640390.1:n.679T>G
ENST00000640469.1:c.113T>G	ENSP00000491875.1:p.Leu38Arg
ENST00000640560.1:n.525T>G
ENST00000640893.1:c.*147T>G	ENSP00000492677.1:n.*147T>G
ENST00000262493.10:c.749T>G	ENSP00000262493.6:p.Leu250Arg
ENST00000568375.1:n.116-3457T>G
NM_020988.2:c.749T>G	NP_066268.1:p.Leu250Arg
XM_011523003.1:c.623T>G	XP_011521305.1:p.Leu208Arg
XM_011523003.3:c.623T>G	XP_011521305.1:p.Leu208Arg
NM_020988.3:c.749T>G MANE Select	NP_066268.1:p.Leu250Arg