Canonical Allele Identifier: CA2695223481

Gene: GNAO1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.765dup MANE Select	ENSP00000262493.6:p.Asn256Ter
ENST00000562316.6:c.432dup	ENSP00000457238.2:p.Asn145Ter
ENST00000564727.2:c.69dup	ENSP00000454971.2:p.Asn24Ter
ENST00000568375.2:c.116-3441dup
ENST00000638185.1:n.980dup
ENST00000638210.1:n.1065dup
ENST00000638705.1:c.765dup	ENSP00000491223.1:p.Asn256Ter
ENST00000638836.1:n.675dup
ENST00000639055.1:n.1486dup
ENST00000639251.1:n.666dup
ENST00000639268.1:c.400dup
ENST00000639341.1:c.290dup
ENST00000639770.1:c.803dup	ENSP00000491999.1:n.803dup
ENST00000640390.1:n.695dup
ENST00000640469.1:c.129dup	ENSP00000491875.1:p.Asn44Ter
ENST00000640560.1:n.541dup
ENST00000640893.1:c.*163dup	ENSP00000492677.1:n.*163dup
ENST00000262493.10:c.765dup	ENSP00000262493.6:p.Asn256Ter
ENST00000568375.1:n.116-3441dup
NM_020988.2:c.765dup	NP_066268.1:p.Asn256Ter
XM_011523003.1:c.639dup	XP_011521305.1:p.Asn214Ter
XM_011523003.3:c.639dup	XP_011521305.1:p.Asn214Ter
NM_020988.3:c.765dup MANE Select	NP_066268.1:p.Asn256Ter