Canonical Allele Identifier: CA15777279
Gene: DAOA HGNC NCBI
DAOA-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.105475787A>C , CM000675.2:g.105475787A>C GRCh38
NC_000013.10:g.106128136A>C , CM000675.1:g.106128136A>C GRCh37
NC_000013.9:g.104926137A>C NCBI36
NG_012694.1:g.14921A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375936.9:c.281+3102A>C (DAOA) MANE Select ENSP00000365103.3:n.281+3102A>C
ENST00000375936.8:c.281+3102A>C (DAOA) ENSP00000365103.3:n.281+3102A>C
ENST00000471432.3:c.388+717A>C (DAOA)
ENST00000329625.9:c.68+3102A>C (DAOA) ENSP00000329951.5:n.68+3102A>C
ENST00000375936.7:c.281+3102A>C (DAOA) ENSP00000365103.3:n.281+3102A>C
ENST00000471432.2:c.387+718A>C (DAOA)
ENST00000473269.5:c.375+717A>C (DAOA) ENSP00000470244.1:n.375+717A>C
ENST00000488534.5:c.162+717A>C (DAOA) ENSP00000471091.1:n.162+717A>C
ENST00000489237.6:c.*84+3102A>C (DAOA) ENSP00000472676.1:n.*84+3102A>C
ENST00000559369.5:c.68+3102A>C (DAOA) ENSP00000453831.1:n.68+3102A>C
ENST00000595812.2:c.88+3102A>C (DAOA) ENSP00000469539.1:n.88+3102A>C
ENST00000600388.5:c.68+3102A>C (DAOA) ENSP00000472260.1:n.68+3102A>C
ENST00000601240.5:c.281+3102A>C (DAOA) ENSP00000471306.1:n.281+3102A>C
ENST00000618629.1:c.281+3102A>C (DAOA) ENSP00000483757.1:n.281+3102A>C
NM_001161812.1:c.88+3102A>C (DAOA) NP_001155284.1:n.88+3102A>C
NM_001161814.1:c.68+3102A>C (DAOA) NP_001155286.1:n.68+3102A>C
NM_172370.4:c.281+3102A>C (DAOA) NP_758958.3:n.281+3102A>C
NR_040247.1:n.506-9367T>G (DAOA-AS1)
XM_005254042.1:c.375+717A>C (DAOA) XP_005254099.1:n.375+717A>C
NM_001384644.1:c.375+717A>C (DAOA) NP_001371573.1:n.375+717A>C
NM_001384645.1:c.74+717A>C (DAOA) NP_001371574.1:n.74+717A>C
NM_001384646.1:c.68+3102A>C (DAOA) NP_001371575.1:n.68+3102A>C
NM_172370.5:c.281+3102A>C (DAOA) MANE Select NP_758958.3:n.281+3102A>C
Search 100 bp 5'
Search 100 bp 3'