Canonical Allele Identifier: CA2062155485

Gene: DAO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108884971T= , CM000674.2:g.108884971T=	GRCh38
NC_000012.11:g.109278747T= , CM000674.1:g.109278747T=	GRCh37
NC_000012.10:g.107802876T=	NCBI36
NG_023236.1:g.9891T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001917.5:c.-9-27T= MANE Select	NP_001908.3:n.-9-27T=
ENST00000228476.8:c.-9-27T= MANE Select	ENSP00000228476.3:n.-9-27T=
NM_001917.4:c.-9-27T=	NP_001908.3:n.-9-27T=
ENST00000228476.7:c.-9-27T=	ENSP00000228476.3:n.-9-27T=
ENST00000547122.5:c.-9-27T=	ENSP00000448095.1:n.-9-27T=
ENST00000547166.1:c.-9-27T=	ENSP00000447104.1:n.-9-27T=
ENST00000547768.5:c.-60-4498T=	ENSP00000449967.1:n.-60-4498T=
ENST00000549215.5:c.-9-27T=	ENSP00000449248.1:n.-9-27T=
ENST00000551281.5:c.-9-27T=	ENSP00000446853.1:n.-9-27T=
XM_005268692.2:c.-9-27T=	XP_005268749.1:n.-9-27T=
XM_005268692.4:c.-9-27T=	XP_005268749.1:n.-9-27T=
XM_011538004.1:c.-9-27T=	XP_011536306.1:n.-9-27T=
XM_011538004.2:c.-9-27T=	XP_011536306.1:n.-9-27T=
XM_011538005.1:c.-9-27T=	XP_011536307.1:n.-9-27T=
XM_011538005.2:c.-9-27T=	XP_011536307.1:n.-9-27T=