Canonical Allele Identifier: CA2224102506

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336815C= , CM000678.2:g.56336815C=	GRCh38
NC_000016.9:g.56370727C= , CM000678.1:g.56370727C=	GRCh37
NC_000016.8:g.54928228C=	NCBI36
NG_042800.1:g.150477C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.678C=	ENSP00000262494.7:p.Val226=
ENST00000262493.12:c.678C= MANE Select	ENSP00000262493.6:p.Val226=
ENST00000262494.12:c.678C=	ENSP00000262494.7:p.Val226=
ENST00000562316.6:c.345C=	ENSP00000457238.2:p.Val115=
ENST00000568375.2:c.70C=
ENST00000638185.1:n.893C=
ENST00000638210.1:n.978C=
ENST00000638705.1:c.678C=	ENSP00000491223.1:p.Val226=
ENST00000638836.1:n.588C=
ENST00000639055.1:n.1399C=
ENST00000639251.1:n.579C=
ENST00000639268.1:c.313C=
ENST00000639341.1:c.203C=
ENST00000639770.1:c.716C=	ENSP00000491999.1:n.716C=
ENST00000640390.1:n.608C=
ENST00000640469.1:c.42C=	ENSP00000491875.1:p.Val14=
ENST00000640560.1:n.454C=
ENST00000640893.1:c.*76C=	ENSP00000492677.1:n.*76C=
ENST00000262493.10:c.678C=	ENSP00000262493.6:p.Val226=
ENST00000262494.11:c.678C=	ENSP00000262494.7:p.Val226=
ENST00000568375.1:n.70C=
NM_020988.2:c.678C=	NP_066268.1:p.Val226=
NM_138736.2:c.678C=	NP_620073.2:p.Val226=
XM_011523003.1:c.552C=	XP_011521305.1:p.Val184=
XM_011523003.3:c.552C=	XP_011521305.1:p.Val184=
NM_020988.3:c.678C= MANE Select	NP_066268.1:p.Val226=
NM_138736.3:c.678C=	NP_620073.2:p.Val226=