Canonical Allele Identifier: CA2116490750

Gene: DAOA DAOA-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.105475180C= , CM000675.2:g.105475180C=	GRCh38
NC_000013.10:g.106127529C= , CM000675.1:g.106127529C=	GRCh37
NC_000013.9:g.104925530C=	NCBI36
NG_012694.1:g.14314C=

Transcript Alleles

HGVS	Amino-acid Change
NM_172370.5:c.281+2495C= (DAOA) MANE Select	NP_758958.3:n.281+2495C=
ENST00000375936.9:c.281+2495C= (DAOA) MANE Select	ENSP00000365103.3:n.281+2495C=
NM_001161812.1:c.88+2495C= (DAOA)	NP_001155284.1:n.88+2495C=
NM_001161814.1:c.68+2495C= (DAOA)	NP_001155286.1:n.68+2495C=
NM_001384644.1:c.375+110C= (DAOA)	NP_001371573.1:n.375+110C=
NM_001384645.1:c.74+110C= (DAOA)	NP_001371574.1:n.74+110C=
NM_001384646.1:c.68+2495C= (DAOA)	NP_001371575.1:n.68+2495C=
NM_172370.4:c.281+2495C= (DAOA)	NP_758958.3:n.281+2495C=
NR_040247.1:n.506-8760G= (DAOA-AS1)
ENST00000329625.9:c.68+2495C= (DAOA)	ENSP00000329951.5:n.68+2495C=
ENST00000375936.7:c.281+2495C= (DAOA)	ENSP00000365103.3:n.281+2495C=
ENST00000375936.8:c.281+2495C= (DAOA)	ENSP00000365103.3:n.281+2495C=
ENST00000471432.2:c.387+111C= (DAOA)
ENST00000471432.3:c.388+110C= (DAOA)
ENST00000473269.5:c.375+110C= (DAOA)	ENSP00000470244.1:n.375+110C=
ENST00000488534.5:c.162+110C= (DAOA)	ENSP00000471091.1:n.162+110C=
ENST00000489237.6:c.*84+2495C= (DAOA)	ENSP00000472676.1:n.*84+2495C=
ENST00000559369.5:c.68+2495C= (DAOA)	ENSP00000453831.1:n.68+2495C=
ENST00000595812.2:c.88+2495C= (DAOA)	ENSP00000469539.1:n.88+2495C=
ENST00000600388.5:c.68+2495C= (DAOA)	ENSP00000472260.1:n.68+2495C=
ENST00000601240.5:c.281+2495C= (DAOA)	ENSP00000471306.1:n.281+2495C=
ENST00000618629.1:c.281+2495C= (DAOA)	ENSP00000483757.1:n.281+2495C=
XM_005254042.1:c.375+110C= (DAOA)	XP_005254099.1:n.375+110C=