Canonical Allele Identifier: CA2224102502

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56336793T= , CM000678.2:g.56336793T=	GRCh38
NC_000016.9:g.56370705T= , CM000678.1:g.56370705T=	GRCh37
NC_000016.8:g.54928206T=	NCBI36
NG_042800.1:g.150455T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262494.13:c.656T=	ENSP00000262494.7:p.Val219=
ENST00000262493.12:c.656T= MANE Select	ENSP00000262493.6:p.Val219=
ENST00000262494.12:c.656T=	ENSP00000262494.7:p.Val219=
ENST00000562316.6:c.323T=	ENSP00000457238.2:p.Val108=
ENST00000568375.2:c.48T=
ENST00000638185.1:n.871T=
ENST00000638210.1:n.956T=
ENST00000638705.1:c.656T=	ENSP00000491223.1:p.Val219=
ENST00000638836.1:n.566T=
ENST00000639055.1:n.1377T=
ENST00000639251.1:n.557T=
ENST00000639268.1:c.291T=
ENST00000639341.1:c.181T=
ENST00000639770.1:c.694T=	ENSP00000491999.1:n.694T=
ENST00000640390.1:n.586T=
ENST00000640469.1:c.20T=	ENSP00000491875.1:p.Val7=
ENST00000640560.1:n.432T=
ENST00000640893.1:c.*54T=	ENSP00000492677.1:n.*54T=
ENST00000262493.10:c.656T=	ENSP00000262493.6:p.Val219=
ENST00000262494.11:c.656T=	ENSP00000262494.7:p.Val219=
ENST00000568375.1:n.48T=
NM_020988.2:c.656T=	NP_066268.1:p.Val219=
NM_138736.2:c.656T=	NP_620073.2:p.Val219=
XM_011523003.1:c.530T=	XP_011521305.1:p.Val177=
XM_011523003.3:c.530T=	XP_011521305.1:p.Val177=
NM_020988.3:c.656T= MANE Select	NP_066268.1:p.Val219=
NM_138736.3:c.656T=	NP_620073.2:p.Val219=