Canonical Allele Identifier: CA15776263
Gene: DAOA HGNC NCBI
DAOA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs947267

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.105487313T>G , CM000675.2:g.105487313T>G GRCh38
NC_000013.10:g.106139662T>G , CM000675.1:g.106139662T>G GRCh37
NC_000013.9:g.104937663T>G NCBI36
NG_012694.1:g.26447T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375936.9:c.282-2588T>G (DAOA) MANE Select ENSP00000365103.3:n.282-2588T>G
ENST00000375936.8:c.282-2588T>G (DAOA) ENSP00000365103.3:n.282-2588T>G
ENST00000471432.3:c.485-2479T>G (DAOA)
ENST00000329625.9:c.69-2588T>G (DAOA) ENSP00000329951.5:n.69-2588T>G
ENST00000375936.7:c.282-2588T>G (DAOA) ENSP00000365103.3:n.282-2588T>G
ENST00000471432.2:c.484-2479T>G (DAOA)
ENST00000473269.5:c.376-2588T>G (DAOA) ENSP00000470244.1:n.376-2588T>G
ENST00000488534.5:c.163-2588T>G (DAOA) ENSP00000471091.1:n.163-2588T>G
ENST00000489237.6:c.*85-2588T>G (DAOA) ENSP00000472676.1:n.*85-2588T>G
ENST00000559369.5:c.69-2588T>G (DAOA) ENSP00000453831.1:n.69-2588T>G
ENST00000595812.2:c.89-2479T>G (DAOA) ENSP00000469539.1:n.89-2479T>G
ENST00000600388.5:c.69-2588T>G (DAOA) ENSP00000472260.1:n.69-2588T>G
ENST00000601240.5:c.282-2479T>G (DAOA) ENSP00000471306.1:n.282-2479T>G
ENST00000618629.1:c.282-2588T>G (DAOA) ENSP00000483757.1:n.282-2588T>G
NM_001161812.1:c.89-2479T>G (DAOA) NP_001155284.1:n.89-2479T>G
NM_001161814.1:c.69-2588T>G (DAOA) NP_001155286.1:n.69-2588T>G
NM_172370.4:c.282-2588T>G (DAOA) NP_758958.3:n.282-2588T>G
NR_040247.1:n.505+2463A>C (DAOA-AS1)
XM_005254042.1:c.376-2588T>G (DAOA) XP_005254099.1:n.376-2588T>G
NM_001384644.1:c.376-2588T>G (DAOA) NP_001371573.1:n.376-2588T>G
NM_001384645.1:c.75-2588T>G (DAOA) NP_001371574.1:n.75-2588T>G
NM_001384646.1:c.69-2588T>G (DAOA) NP_001371575.1:n.69-2588T>G
NM_172370.5:c.282-2588T>G (DAOA) MANE Select NP_758958.3:n.282-2588T>G