Canonical Allele Identifier: CA2580089803

Gene: DNAAF4 DNAAF4-CCPG1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.55439472_55439581del , CM000677.2:g.55439472_55439581del	GRCh38
NC_000015.9:g.55731670_55731779del , CM000677.1:g.55731670_55731779del	GRCh37
NC_000015.8:g.53518962_53519071del	NCBI36
NG_021213.1:g.73654_73763del

Transcript Alleles

HGVS	Amino-acid Change
NM_130810.4:c.784_893del (DNAAF4) MANE Select	NP_570722.2:p.Trp262GlnfsTer16
ENST00000321149.7:c.784_893del (DNAAF4) MANE Select	ENSP00000323275.3:p.Trp262GlnfsTer16
NM_001033559.2:c.784_893del (DNAAF4)	NP_001028731.1:p.Trp262GlnfsTer16
NM_001033559.3:c.784_893del (DNAAF4)	NP_001028731.1:p.Trp262GlnfsTer16
NM_001033560.1:c.784_893del (DNAAF4)	NP_001028732.1:p.Trp262GlnfsTer16
NM_001033560.2:c.784_893del (DNAAF4)	NP_001028732.1:p.Trp262GlnfsTer16
NM_130810.3:c.784_893del (DNAAF4)	NP_570722.2:p.Trp262GlnfsTer16
NR_037923.1:n.1039_1148del (DNAAF4-CCPG1)
ENST00000348518.4:c.784_893del (DNAAF4)	ENSP00000299561.5:p.Trp262GlnfsTer16
ENST00000448430.6:c.784_893del (DNAAF4)	ENSP00000403412.2:p.Trp262GlnfsTer16
ENST00000457155.6:c.784_893del (DNAAF4)	ENSP00000402640.2:p.Trp262GlnfsTer16
ENST00000524160.5:c.*111_*220del (DNAAF4)	ENSP00000428097.1:n.*111_*220del