Canonical Allele Identifier: CA2767243978
Gene: XRCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83353184del , CM000667.2:g.83353184del GRCh38
NC_000005.9:g.82649003del , CM000667.1:g.82649003del GRCh37
NC_000005.8:g.82684759del NCBI36
NG_047086.1:g.280776del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396027.9:c.947del MANE Select ENSP00000379344.4:p.Asn316ThrfsTer4
ENST00000282268.7:c.947del ENSP00000282268.3:p.Asn316ThrfsTer4
ENST00000338635.10:c.953del ENSP00000342011.6:p.Asn318ThrfsTer4
ENST00000396027.8:c.947del ENSP00000379344.4:p.Asn316ThrfsTer4
ENST00000511817.1:c.953del ENSP00000421491.1:p.Asn318ThrfsTer4
NM_003401.3:c.947del NP_003392.1:p.Asn316ThrfsTer4
NM_022406.2:c.953del NP_071801.1:p.Asn318ThrfsTer4
NM_022550.2:c.947del NP_072044.1:p.Asn316ThrfsTer4
XM_005248595.1:c.953del XP_005248652.1:p.Asn318ThrfsTer4
XM_011543626.1:c.953del XP_011541928.1:p.Asn318ThrfsTer4
XM_011543629.1:c.293del XP_011541931.1:p.Asn98ThrfsTer4
NM_001318012.1:c.953del NP_001304941.1:p.Asn318ThrfsTer4
NM_003401.4:c.947del NP_003392.1:p.Asn316ThrfsTer4
NM_022406.3:c.953del NP_071801.1:p.Asn318ThrfsTer4
NM_022550.3:c.947del NP_072044.1:p.Asn316ThrfsTer4
XM_017009827.2:c.894-17083del XP_016865316.1:n.894-17083del
NM_001318012.2:c.953del NP_001304941.1:p.Asn318ThrfsTer4
NM_003401.5:c.947del MANE Select NP_003392.1:p.Asn316ThrfsTer4
NM_022406.4:c.953del NP_071801.1:p.Asn318ThrfsTer4
NM_001318012.3:c.953del NP_001304941.1:p.Asn318ThrfsTer4
NM_022406.5:c.953del NP_071801.1:p.Asn318ThrfsTer4
NM_022550.4:c.947del NP_072044.1:p.Asn316ThrfsTer4