Canonical Allele Identifier: CA2674491790
Gene: XRCC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83353339_83353348dup , CM000667.2:g.83353339_83353348dup GRCh38
NC_000005.9:g.82649158_82649167dup , CM000667.1:g.82649158_82649167dup GRCh37
NC_000005.8:g.82684914_82684923dup NCBI36
NG_047086.1:g.280931_280940dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000396027.9:c.*97_*106dup MANE Select ENSP00000379344.4:n.*97_*106dup
ENST00000282268.7:c.*97_*106dup ENSP00000282268.3:n.*97_*106dup
ENST00000338635.10:c.*97_*106dup ENSP00000342011.6:n.*97_*106dup
ENST00000396027.8:c.*97_*106dup ENSP00000379344.4:n.*97_*106dup
ENST00000511817.1:c.*97_*106dup ENSP00000421491.1:n.*97_*106dup
NM_003401.3:c.*97_*106dup NP_003392.1:n.*97_*106dup
NM_022406.2:c.*97_*106dup NP_071801.1:n.*97_*106dup
NM_022550.2:c.*97_*106dup NP_072044.1:n.*97_*106dup
XM_005248595.1:c.*97_*106dup XP_005248652.1:n.*97_*106dup
XM_011543626.1:c.*97_*106dup XP_011541928.1:n.*97_*106dup
XM_011543629.1:c.*97_*106dup XP_011541931.1:n.*97_*106dup
NM_001318012.1:c.*97_*106dup NP_001304941.1:n.*97_*106dup
NM_003401.4:c.*97_*106dup NP_003392.1:n.*97_*106dup
NM_022406.3:c.*97_*106dup NP_071801.1:n.*97_*106dup
NM_022550.3:c.*97_*106dup NP_072044.1:n.*97_*106dup
XM_017009827.2:c.894-16928_894-16919dup XP_016865316.1:n.894-16928_894-16919dup
NM_001318012.2:c.*97_*106dup NP_001304941.1:n.*97_*106dup
NM_003401.5:c.*97_*106dup MANE Select NP_003392.1:n.*97_*106dup
NM_022406.4:c.*97_*106dup NP_071801.1:n.*97_*106dup
NM_001318012.3:c.*97_*106dup NP_001304941.1:n.*97_*106dup
NM_022406.5:c.*97_*106dup NP_071801.1:n.*97_*106dup
NM_022550.4:c.*97_*106dup NP_072044.1:n.*97_*106dup