Canonical Allele Identifier: CA2062126751

Gene: DAO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108899544A= , CM000674.2:g.108899544A=	GRCh38
NC_000012.11:g.109293320A= , CM000674.1:g.109293320A=	GRCh37
NC_000012.10:g.107817449A=	NCBI36
NG_023236.1:g.24464A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228476.8:c.912+69A= MANE Select	ENSP00000228476.3:n.912+69A=
ENST00000228476.7:c.912+69A=	ENSP00000228476.3:n.912+69A=
ENST00000546552.1:n.424+69A=
ENST00000547122.5:c.*560+69A=	ENSP00000448095.1:n.*560+69A=
ENST00000549215.5:c.*532A=	ENSP00000449248.1:n.*532A=
ENST00000551281.5:c.714+69A=	ENSP00000446853.1:n.714+69A=
NM_001917.4:c.912+69A=	NP_001908.3:n.912+69A=
XM_005268692.2:c.846+69A=	XP_005268749.1:n.846+69A=
XM_011538004.1:c.912+69A=	XP_011536306.1:n.912+69A=
XM_011538005.1:c.912+69A=	XP_011536307.1:n.912+69A=
XM_005268692.4:c.846+69A=	XP_005268749.1:n.846+69A=
XM_011538004.2:c.912+69A=	XP_011536306.1:n.912+69A=
XM_011538005.2:c.912+69A=	XP_011536307.1:n.912+69A=
NM_001917.5:c.912+69A= MANE Select	NP_001908.3:n.912+69A=