Canonical Allele Identifier: CA2224110116

Gene: GNAO1

Linked Data

• dbSNP Id: rs2037953880

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354885_56354886insAAG , CM000678.2:g.56354885_56354886insAAG	GRCh38
NC_000016.9:g.56388797_56388798insAAG , CM000678.1:g.56388797_56388798insAAG	GRCh37
NC_000016.8:g.54946298_54946299insAAG	NCBI36
NG_042800.1:g.168547_168548insAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.897_898insAAG MANE Select	ENSP00000262493.6:p.Asp299_Ala300insLys
ENST00000562316.6:c.545-1218_545-1217insAAG	ENSP00000457238.2:n.545-1218_545-1217insAAG
ENST00000564727.2:c.201_202insAAG	ENSP00000454971.2:p.Asp67_Ala68insLys
ENST00000568375.2:c.135_136insAAG
ENST00000638185.1:n.1112_1113insAAG
ENST00000638210.1:n.1197_1198insAAG
ENST00000638705.1:c.897_898insAAG	ENSP00000491223.1:p.Asp299_Ala300insLys
ENST00000638836.1:n.807_808insAAG
ENST00000639055.1:n.1618_1619insAAG
ENST00000639251.1:n.798_799insAAG
ENST00000639268.1:c.532_533insAAG
ENST00000639341.1:c.422_423insAAG
ENST00000639770.1:c.935_936insAAG	ENSP00000491999.1:n.935_936insAAG
ENST00000640390.1:n.827_828insAAG
ENST00000640469.1:c.261_262insAAG	ENSP00000491875.1:p.Asp87_Ala88insLys
ENST00000640560.1:n.673_674insAAG
ENST00000640893.1:c.*295_*296insAAG	ENSP00000492677.1:n.*295_*296insAAG
ENST00000262493.10:c.897_898insAAG	ENSP00000262493.6:p.Asp299_Ala300insLys
ENST00000564727.1:c.117_118insAAG	ENSP00000454971.1:p.Asp39_Ala40insLys
ENST00000568375.1:n.135_136insAAG
NM_020988.2:c.897_898insAAG	NP_066268.1:p.Asp299_Ala300insLys
XM_011523003.1:c.771_772insAAG	XP_011521305.1:p.Asp257_Ala258insLys
XM_011523003.3:c.771_772insAAG	XP_011521305.1:p.Asp257_Ala258insLys
NM_020988.3:c.897_898insAAG MANE Select	NP_066268.1:p.Asp299_Ala300insLys