Canonical Allele Identifier: CA495585902

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56388803C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354891C>A , CM000678.2:g.56354891C>A	GRCh38
NC_000016.9:g.56388803C>A , CM000678.1:g.56388803C>A	GRCh37
NC_000016.8:g.54946304C>A	NCBI36
NG_042800.1:g.168553C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.903C>A MANE Select	ENSP00000262493.6:p.Ala301=
ENST00000562316.6:c.545-1212C>A	ENSP00000457238.2:n.545-1212C>A
ENST00000564727.2:c.207C>A	ENSP00000454971.2:p.Ala69=
ENST00000568375.2:c.141C>A
ENST00000638185.1:n.1118C>A
ENST00000638210.1:n.1203C>A
ENST00000638705.1:c.903C>A	ENSP00000491223.1:p.Ala301=
ENST00000638836.1:n.813C>A
ENST00000639055.1:n.1624C>A
ENST00000639251.1:n.804C>A
ENST00000639268.1:c.538C>A
ENST00000639341.1:c.428C>A
ENST00000639770.1:c.941C>A	ENSP00000491999.1:n.941C>A
ENST00000640390.1:n.833C>A
ENST00000640469.1:c.267C>A	ENSP00000491875.1:p.Ala89=
ENST00000640560.1:n.679C>A
ENST00000640893.1:c.*301C>A	ENSP00000492677.1:n.*301C>A
ENST00000262493.10:c.903C>A	ENSP00000262493.6:p.Ala301=
ENST00000564727.1:c.123C>A	ENSP00000454971.1:p.Ala41=
ENST00000568375.1:n.141C>A
NM_020988.2:c.903C>A	NP_066268.1:p.Ala301=
XM_011523003.1:c.777C>A	XP_011521305.1:p.Ala259=
XM_011523003.3:c.777C>A	XP_011521305.1:p.Ala259=
NM_020988.3:c.903C>A MANE Select	NP_066268.1:p.Ala301=