Canonical Allele Identifier: CA2343276864

Gene: DNAAF3 DNAAF3-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55159354G= , CM000681.2:g.55159354G=	GRCh38
NC_000019.9:g.55670722G= , CM000681.1:g.55670722G=	GRCh37
NC_000019.8:g.60362534G=	NCBI36
NG_007866.2:g.3379C= , LRG_432:g.3379C=
NG_032759.1:g.12369C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000524407.7:c.1334C= (DNAAF3) MANE Select	ENSP00000432046.3:p.Ala445=
ENST00000391720.8:c.1475C= (DNAAF3)	ENSP00000375600.5:p.Ala492=
ENST00000455045.5:c.1172C= (DNAAF3)	ENSP00000394343.1:p.Ala391=
ENST00000524407.6:c.1334C= (DNAAF3)	ENSP00000432046.2:p.Ala445=
ENST00000527223.6:c.1535C= (DNAAF3)	ENSP00000436975.2:p.Ala512=
ENST00000528412.5:c.*1122C= (DNAAF3)	ENSP00000433826.2:n.*1122C=
ENST00000533527.6:n.1096C= (DNAAF3)
ENST00000587789.2:n.419C= (DNAAF3)
ENST00000587871.1:c.318C=
ENST00000588076.1:c.333C= (DNAAF3)
NM_001256714.1:c.1535C= (DNAAF3)	NP_001243643.1:p.Ala512=
NM_001256715.1:c.1334C= (DNAAF3)	NP_001243644.1:p.Ala445=
NM_001256716.1:c.1172C= (DNAAF3)	NP_001243645.1:p.Ala391=
NM_178837.4:c.1475C= (DNAAF3)	NP_849159.2:p.Ala492=
XR_001754015.1:n.16G= (DNAAF3-AS1)
NM_001256715.2:c.1334C= (DNAAF3) MANE Select	NP_001243644.1:p.Ala445=
NM_001256716.2:c.1172C= (DNAAF3)	NP_001243645.1:p.Ala391=