Canonical Allele Identifier: CA388691590

Gene: DAOA DAOA-AS1

Linked Data

• MyVariant Identifiers: chr13:g.106124976A>T (hg19) ; chr13:g.105472627A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.105472627A>T , CM000675.2:g.105472627A>T	GRCh38
NC_000013.10:g.106124976A>T , CM000675.1:g.106124976A>T	GRCh37
NC_000013.9:g.104922977A>T	NCBI36
NG_012694.1:g.11761A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375936.9:c.223A>T (DAOA) MANE Select	ENSP00000365103.3:p.Arg75Trp
ENST00000375936.8:c.223A>T (DAOA)	ENSP00000365103.3:p.Arg75Trp
ENST00000471432.3:c.236A>T (DAOA)
ENST00000329625.9:c.10A>T (DAOA)	ENSP00000329951.5:p.Arg4Trp
ENST00000375936.7:c.223A>T (DAOA)	ENSP00000365103.3:p.Arg75Trp
ENST00000471432.2:c.236A>T (DAOA)
ENST00000473269.5:c.223A>T (DAOA)	ENSP00000470244.1:p.Arg75Trp
ENST00000488534.5:c.10A>T (DAOA)	ENSP00000471091.1:p.Arg4Trp
ENST00000489237.6:c.*26A>T (DAOA)	ENSP00000472676.1:n.*26A>T
ENST00000559369.5:c.10A>T (DAOA)	ENSP00000453831.1:p.Arg4Trp
ENST00000595812.2:c.30A>T (DAOA)	ENSP00000469539.1:p.Arg10Ser
ENST00000600388.5:c.10A>T (DAOA)	ENSP00000472260.1:p.Arg4Trp
ENST00000601240.5:c.223A>T (DAOA)	ENSP00000471306.1:p.Arg75Trp
ENST00000618629.1:c.223A>T (DAOA)	ENSP00000483757.1:p.Arg75Trp
NM_001161812.1:c.30A>T (DAOA)	NP_001155284.1:p.Arg10Ser
NM_001161814.1:c.10A>T (DAOA)	NP_001155286.1:p.Arg4Trp
NM_172370.4:c.223A>T (DAOA)	NP_758958.3:p.Arg75Trp
NR_040247.1:n.506-6207T>A (DAOA-AS1)
XM_005254042.1:c.223A>T (DAOA)	XP_005254099.1:p.Arg75Trp
NM_001384644.1:c.223A>T (DAOA)	NP_001371573.1:p.Arg75Trp
NM_001384645.1:c.-79A>T (DAOA)	NP_001371574.1:n.-79A>T
NM_001384646.1:c.10A>T (DAOA)	NP_001371575.1:p.Arg4Trp
NM_172370.5:c.223A>T (DAOA) MANE Select	NP_758958.3:p.Arg75Trp