Canonical Allele Identifier: CA2224108736

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351417T= , CM000678.2:g.56351417T=	GRCh38
NC_000016.9:g.56385329T= , CM000678.1:g.56385329T=	GRCh37
NC_000016.8:g.54942830T=	NCBI36
NG_042800.1:g.165079T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.757T= MANE Select	ENSP00000262493.6:p.Ser253=
ENST00000562316.6:c.424T=	ENSP00000457238.2:p.Ser142=
ENST00000564727.2:c.61T=	ENSP00000454971.2:p.Ser21=
ENST00000568375.2:c.116-3449T=
ENST00000638185.1:n.972T=
ENST00000638210.1:n.1057T=
ENST00000638705.1:c.757T=	ENSP00000491223.1:p.Ser253=
ENST00000638836.1:n.667T=
ENST00000639055.1:n.1478T=
ENST00000639251.1:n.658T=
ENST00000639268.1:c.392T=
ENST00000639341.1:c.282T=
ENST00000639770.1:c.795T=	ENSP00000491999.1:n.795T=
ENST00000640390.1:n.687T=
ENST00000640469.1:c.121T=	ENSP00000491875.1:p.Ser41=
ENST00000640560.1:n.533T=
ENST00000640893.1:c.*155T=	ENSP00000492677.1:n.*155T=
ENST00000262493.10:c.757T=	ENSP00000262493.6:p.Ser253=
ENST00000568375.1:n.116-3449T=
NM_020988.2:c.757T=	NP_066268.1:p.Ser253=
XM_011523003.1:c.631T=	XP_011521305.1:p.Ser211=
XM_011523003.3:c.631T=	XP_011521305.1:p.Ser211=
NM_020988.3:c.757T= MANE Select	NP_066268.1:p.Ser253=