Canonical Allele Identifier: CA2224102494

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336757C= , CM000678.2:g.56336757C=	GRCh38
NC_000016.9:g.56370669C= , CM000678.1:g.56370669C=	GRCh37
NC_000016.8:g.54928170C=	NCBI36
NG_042800.1:g.150419C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.620C=	ENSP00000262494.7:p.Ser207=
ENST00000262493.12:c.620C= MANE Select	ENSP00000262493.6:p.Ser207=
ENST00000262494.12:c.620C=	ENSP00000262494.7:p.Ser207=
ENST00000562316.6:c.287C=	ENSP00000457238.2:p.Ser96=
ENST00000568375.2:c.12C=
ENST00000638185.1:n.835C=
ENST00000638210.1:n.920C=
ENST00000638705.1:c.620C=	ENSP00000491223.1:p.Ser207=
ENST00000638836.1:n.530C=
ENST00000639055.1:n.1341C=
ENST00000639251.1:n.521C=
ENST00000639268.1:c.255C=
ENST00000639341.1:c.145C=
ENST00000639770.1:c.658C=	ENSP00000491999.1:n.658C=
ENST00000640390.1:n.550C=
ENST00000640560.1:n.396C=
ENST00000640893.1:c.*18C=	ENSP00000492677.1:n.*18C=
ENST00000262493.10:c.620C=	ENSP00000262493.6:p.Ser207=
ENST00000262494.11:c.620C=	ENSP00000262494.7:p.Ser207=
ENST00000568375.1:n.12C=
NM_020988.2:c.620C=	NP_066268.1:p.Ser207=
NM_138736.2:c.620C=	NP_620073.2:p.Ser207=
XM_011523003.1:c.494C=	XP_011521305.1:p.Ser165=
XM_011523003.3:c.494C=	XP_011521305.1:p.Ser165=
NM_020988.3:c.620C= MANE Select	NP_066268.1:p.Ser207=
NM_138736.3:c.620C=	NP_620073.2:p.Ser207=