Canonical Allele Identifier: CA2018061970
Gene: DAOA HGNC NCBI
DAOA-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.105467097G= , CM000675.2:g.105467097G= GRCh38
NC_000013.10:g.106119446G= , CM000675.1:g.106119446G= GRCh37
NC_000013.9:g.104917447G= NCBI36
NG_012694.1:g.6231G=

Transcript Alleles

HGVS Amino-acid Change
NM_172370.5:c.89G= (DAOA) MANE Select NP_758958.3:p.Arg30=
ENST00000375936.9:c.89G= (DAOA) MANE Select ENSP00000365103.3:p.Arg30=
NM_001161812.1:c.-105G= (DAOA) NP_001155284.1:n.-105G=
NM_001161814.1:c.-125G= (DAOA) NP_001155286.1:n.-125G=
NM_001384644.1:c.89G= (DAOA) NP_001371573.1:p.Arg30=
NM_001384645.1:c.-213G= (DAOA) NP_001371574.1:n.-213G=
NM_001384646.1:c.-125G= (DAOA) NP_001371575.1:n.-125G=
NM_172370.4:c.89G= (DAOA) NP_758958.3:p.Arg30=
NR_040247.1:n.506-677C= (DAOA-AS1)
ENST00000329625.9:c.-125G= (DAOA) ENSP00000329951.5:n.-125G=
ENST00000375936.7:c.89G= (DAOA) ENSP00000365103.3:p.Arg30=
ENST00000375936.8:c.89G= (DAOA) ENSP00000365103.3:p.Arg30=
ENST00000473269.5:c.89G= (DAOA) ENSP00000470244.1:p.Arg30=
ENST00000488534.5:c.-125G= (DAOA) ENSP00000471091.1:n.-125G=
ENST00000489237.6:c.89G= (DAOA) ENSP00000472676.1:p.Arg30=
ENST00000559369.5:c.-125G= (DAOA) ENSP00000453831.1:n.-125G=
ENST00000595812.2:c.-105G= (DAOA) ENSP00000469539.1:n.-105G=
ENST00000600388.5:c.-125G= (DAOA) ENSP00000472260.1:n.-125G=
ENST00000601240.5:c.89G= (DAOA) ENSP00000471306.1:p.Arg30=
ENST00000618629.1:c.89G= (DAOA) ENSP00000483757.1:p.Arg30=
XM_005254042.1:c.89G= (DAOA) XP_005254099.1:p.Arg30=