Canonical Allele Identifier: CA2224108749

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351471A= , CM000678.2:g.56351471A=	GRCh38
NC_000016.9:g.56385383A= , CM000678.1:g.56385383A=	GRCh37
NC_000016.8:g.54942884A=	NCBI36
NG_042800.1:g.165133A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.811A= MANE Select	ENSP00000262493.6:p.Lys271=
ENST00000562316.6:c.478A=	ENSP00000457238.2:p.Lys160=
ENST00000564727.2:c.115A=	ENSP00000454971.2:p.Lys39=
ENST00000568375.2:c.116-3395A=
ENST00000638185.1:n.1026A=
ENST00000638210.1:n.1111A=
ENST00000638705.1:c.811A=	ENSP00000491223.1:p.Lys271=
ENST00000638836.1:n.721A=
ENST00000639055.1:n.1532A=
ENST00000639251.1:n.712A=
ENST00000639268.1:c.446A=
ENST00000639341.1:c.336A=
ENST00000639770.1:c.849A=	ENSP00000491999.1:n.849A=
ENST00000640390.1:n.741A=
ENST00000640469.1:c.175A=	ENSP00000491875.1:p.Lys59=
ENST00000640560.1:n.587A=
ENST00000640893.1:c.*209A=	ENSP00000492677.1:n.*209A=
ENST00000262493.10:c.811A=	ENSP00000262493.6:p.Lys271=
ENST00000564727.1:c.31A=	ENSP00000454971.1:p.Lys11=
ENST00000568375.1:n.116-3395A=
NM_020988.2:c.811A=	NP_066268.1:p.Lys271=
XM_011523003.1:c.685A=	XP_011521305.1:p.Lys229=
XM_011523003.3:c.685A=	XP_011521305.1:p.Lys229=
NM_020988.3:c.811A= MANE Select	NP_066268.1:p.Lys271=