Canonical Allele Identifier: CA2224108728

Gene: GNAO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351394A= , CM000678.2:g.56351394A=	GRCh38
NC_000016.9:g.56385306A= , CM000678.1:g.56385306A=	GRCh37
NC_000016.8:g.54942807A=	NCBI36
NG_042800.1:g.165056A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.734A= MANE Select	ENSP00000262493.6:p.His245=
ENST00000562316.6:c.401A=	ENSP00000457238.2:p.His134=
ENST00000564727.2:c.38A=	ENSP00000454971.2:p.His13=
ENST00000568375.2:c.116-3472A=
ENST00000638185.1:n.949A=
ENST00000638210.1:n.1034A=
ENST00000638705.1:c.734A=	ENSP00000491223.1:p.His245=
ENST00000638836.1:n.644A=
ENST00000639055.1:n.1455A=
ENST00000639251.1:n.635A=
ENST00000639268.1:c.369A=
ENST00000639341.1:c.259A=
ENST00000639770.1:c.772A=	ENSP00000491999.1:n.772A=
ENST00000640390.1:n.664A=
ENST00000640469.1:c.98A=	ENSP00000491875.1:p.His33=
ENST00000640560.1:n.510A=
ENST00000640893.1:c.*132A=	ENSP00000492677.1:n.*132A=
ENST00000262493.10:c.734A=	ENSP00000262493.6:p.His245=
ENST00000568375.1:n.116-3472A=
NM_020988.2:c.734A=	NP_066268.1:p.His245=
XM_011523003.1:c.608A=	XP_011521305.1:p.His203=
XM_011523003.3:c.608A=	XP_011521305.1:p.His203=
NM_020988.3:c.734A= MANE Select	NP_066268.1:p.His245=