Canonical Allele Identifier: CA13713503
Gene: DAO HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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