Canonical Allele Identifier: CA2224101538

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56334785A= , CM000678.2:g.56334785A=	GRCh38
NC_000016.9:g.56368697A= , CM000678.1:g.56368697A=	GRCh37
NC_000016.8:g.54926198A=	NCBI36
NG_042800.1:g.148447A=

Transcript Alleles

HGVS	Amino-acid Change
NM_020988.3:c.521A= MANE Select	NP_066268.1:p.Asp174=
ENST00000262493.12:c.521A= MANE Select	ENSP00000262493.6:p.Asp174=
NM_020988.2:c.521A=	NP_066268.1:p.Asp174=
NM_138736.2:c.521A=	NP_620073.2:p.Asp174=
NM_138736.3:c.521A=	NP_620073.2:p.Asp174=
ENST00000262493.10:c.521A=	ENSP00000262493.6:p.Asp174=
ENST00000262494.11:c.521A=	ENSP00000262494.7:p.Asp174=
ENST00000262494.12:c.521A=	ENSP00000262494.7:p.Asp174=
ENST00000262494.13:c.521A=	ENSP00000262494.7:p.Asp174=
ENST00000562316.5:c.260A=	ENSP00000457238.1:p.Asp87=
ENST00000562316.6:c.188A=	ENSP00000457238.2:p.Asp63=
ENST00000638185.1:n.736A=
ENST00000638210.1:n.821A=
ENST00000638705.1:c.521A=	ENSP00000491223.1:p.Asp174=
ENST00000638836.1:n.431A=
ENST00000639055.1:n.1242A=
ENST00000639251.1:n.422A=
ENST00000639268.1:c.229-1946A=
ENST00000639341.1:c.46A=
ENST00000639770.1:c.559A=	ENSP00000491999.1:n.559A=
ENST00000640390.1:n.451A=
ENST00000640893.1:c.360A=	ENSP00000492677.1:p.Gly120=
XM_011523003.1:c.395A=	XP_011521305.1:p.Asp132=
XM_011523003.3:c.395A=	XP_011521305.1:p.Asp132=