Canonical Allele Identifier: CA2062158215

Gene: DAO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108888108G= , CM000674.2:g.108888108G=	GRCh38
NC_000012.11:g.109281884G= , CM000674.1:g.109281884G=	GRCh37
NC_000012.10:g.107806013G=	NCBI36
NG_023236.1:g.13028G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228476.8:c.309+544G= MANE Select	ENSP00000228476.3:n.309+544G=
ENST00000228476.7:c.309+544G=	ENSP00000228476.3:n.309+544G=
ENST00000547122.5:c.195-1361G=	ENSP00000448095.1:n.195-1361G=
ENST00000547166.1:c.309+544G=	ENSP00000447104.1:n.309+544G=
ENST00000547768.5:c.-60-1361G=	ENSP00000449967.1:n.-60-1361G=
ENST00000549215.5:c.309+544G=	ENSP00000449248.1:n.309+544G=
ENST00000551281.5:c.309+544G=	ENSP00000446853.1:n.309+544G=
NM_001917.4:c.309+544G=	NP_001908.3:n.309+544G=
XM_005268692.2:c.309+544G=	XP_005268749.1:n.309+544G=
XM_011538004.1:c.309+544G=	XP_011536306.1:n.309+544G=
XM_011538005.1:c.309+544G=	XP_011536307.1:n.309+544G=
XM_005268692.4:c.309+544G=	XP_005268749.1:n.309+544G=
XM_011538004.2:c.309+544G=	XP_011536306.1:n.309+544G=
XM_011538005.2:c.309+544G=	XP_011536307.1:n.309+544G=
NM_001917.5:c.309+544G= MANE Select	NP_001908.3:n.309+544G=