Canonical Allele Identifier: CA2062158957

Gene: DAO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108889827A= , CM000674.2:g.108889827A=	GRCh38
NC_000012.11:g.109283603A= , CM000674.1:g.109283603A=	GRCh37
NC_000012.10:g.107807732A=	NCBI36
NG_023236.1:g.14747A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001917.5:c.386+282A= MANE Select	NP_001908.3:n.386+282A=
ENST00000228476.8:c.386+282A= MANE Select	ENSP00000228476.3:n.386+282A=
NM_001917.4:c.386+282A=	NP_001908.3:n.386+282A=
ENST00000228476.7:c.386+282A=	ENSP00000228476.3:n.386+282A=
ENST00000547122.5:c.*34+282A=	ENSP00000448095.1:n.*34+282A=
ENST00000547166.1:c.386+282A=	ENSP00000447104.1:n.386+282A=
ENST00000547768.5:c.17+282A=	ENSP00000449967.1:n.17+282A=
ENST00000549215.5:c.310-381A=	ENSP00000449248.1:n.310-381A=
ENST00000551281.5:c.309+2263A=	ENSP00000446853.1:n.309+2263A=
XM_005268692.2:c.386+282A=	XP_005268749.1:n.386+282A=
XM_005268692.4:c.386+282A=	XP_005268749.1:n.386+282A=
XM_011538004.1:c.386+282A=	XP_011536306.1:n.386+282A=
XM_011538004.2:c.386+282A=	XP_011536306.1:n.386+282A=
XM_011538005.1:c.386+282A=	XP_011536307.1:n.386+282A=
XM_011538005.2:c.386+282A=	XP_011536307.1:n.386+282A=