Canonical Allele Identifier: CA2224108942

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351935G= , CM000678.2:g.56351935G=	GRCh38
NC_000016.9:g.56385847G= , CM000678.1:g.56385847G=	GRCh37
NC_000016.8:g.54943348G=	NCBI36
NG_042800.1:g.165597G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.877+398G= MANE Select	ENSP00000262493.6:n.877+398G=
ENST00000562316.6:c.544+398G=	ENSP00000457238.2:n.544+398G=
ENST00000564727.2:c.181+398G=	ENSP00000454971.2:n.181+398G=
ENST00000568375.2:c.116-2931G=
ENST00000638185.1:n.1092+398G=
ENST00000638210.1:n.1177+398G=
ENST00000638705.1:c.877+398G=	ENSP00000491223.1:n.877+398G=
ENST00000638836.1:n.787+398G=
ENST00000639055.1:n.1598+398G=
ENST00000639251.1:n.778+398G=
ENST00000639268.1:c.512+398G=
ENST00000639341.1:c.402+398G=
ENST00000639770.1:c.915+398G=	ENSP00000491999.1:n.915+398G=
ENST00000640390.1:n.807+398G=
ENST00000640469.1:c.241+398G=	ENSP00000491875.1:n.241+398G=
ENST00000640560.1:n.653+398G=
ENST00000640893.1:c.*275+398G=	ENSP00000492677.1:n.*275+398G=
ENST00000262493.10:c.877+398G=	ENSP00000262493.6:n.877+398G=
ENST00000564727.1:c.97+398G=	ENSP00000454971.1:n.97+398G=
ENST00000568375.1:n.116-2931G=
NM_020988.2:c.877+398G=	NP_066268.1:n.877+398G=
XM_011523003.1:c.751+398G=	XP_011521305.1:n.751+398G=
XM_011523003.3:c.751+398G=	XP_011521305.1:n.751+398G=
NM_020988.3:c.877+398G= MANE Select	NP_066268.1:n.877+398G=