Canonical Allele Identifier: CA2674491709
Gene: XRCC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83353082del , CM000667.2:g.83353082del GRCh38
NC_000005.9:g.82648901del , CM000667.1:g.82648901del GRCh37
NC_000005.8:g.82684657del NCBI36
NG_047086.1:g.280674del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396027.9:c.894-49del MANE Select ENSP00000379344.4:n.894-49del
ENST00000282268.7:c.894-49del ENSP00000282268.3:n.894-49del
ENST00000338635.10:c.894-43del ENSP00000342011.6:n.894-43del
ENST00000396027.8:c.894-49del ENSP00000379344.4:n.894-49del
ENST00000511817.1:c.894-43del ENSP00000421491.1:n.894-43del
NM_003401.3:c.894-49del NP_003392.1:n.894-49del
NM_022406.2:c.894-43del NP_071801.1:n.894-43del
NM_022550.2:c.894-49del NP_072044.1:n.894-49del
XM_005248595.1:c.894-43del XP_005248652.1:n.894-43del
XM_011543626.1:c.894-43del XP_011541928.1:n.894-43del
XM_011543629.1:c.234-43del XP_011541931.1:n.234-43del
NM_001318012.1:c.894-43del NP_001304941.1:n.894-43del
NM_003401.4:c.894-49del NP_003392.1:n.894-49del
NM_022406.3:c.894-43del NP_071801.1:n.894-43del
NM_022550.3:c.894-49del NP_072044.1:n.894-49del
XM_017009827.2:c.894-17185del XP_016865316.1:n.894-17185del
NM_001318012.2:c.894-43del NP_001304941.1:n.894-43del
NM_003401.5:c.894-49del MANE Select NP_003392.1:n.894-49del
NM_022406.4:c.894-43del NP_071801.1:n.894-43del
NM_001318012.3:c.894-43del NP_001304941.1:n.894-43del
NM_022406.5:c.894-43del NP_071801.1:n.894-43del
NM_022550.4:c.894-49del NP_072044.1:n.894-49del