Canonical Allele Identifier: CA561260232
Gene: XRCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1962334
ClinVar RCV Id: RCV002726056
dbSNP Id: rs1561332950

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83111067del , CM000667.2:g.83111067del GRCh38
NC_000005.9:g.82406886del , CM000667.1:g.82406886del GRCh37
NC_000005.8:g.82442642del NCBI36
NG_047086.1:g.38659del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396027.9:c.179del MANE Select ENSP00000379344.4:p.Ala60GlufsTer11
ENST00000282268.7:c.179del ENSP00000282268.3:p.Ala60GlufsTer11
ENST00000338635.10:c.179del ENSP00000342011.6:p.Ala60GlufsTer11
ENST00000396027.8:c.179del ENSP00000379344.4:p.Ala60GlufsTer11
ENST00000509268.1:n.191del
ENST00000511817.1:c.179del ENSP00000421491.1:p.Ala60GlufsTer11
ENST00000542685.5:n.248del
NM_003401.3:c.179del NP_003392.1:p.Ala60GlufsTer11
NM_022406.2:c.179del NP_071801.1:p.Ala60GlufsTer11
NM_022550.2:c.179del NP_072044.1:p.Ala60GlufsTer11
XM_005248595.1:c.179del XP_005248652.1:p.Ala60GlufsTer11
XM_011543626.1:c.179del XP_011541928.1:p.Ala60GlufsTer11
XM_011543627.1:c.179del XP_011541929.1:p.Ala60GlufsTer11
XM_011543628.1:c.179del XP_011541930.1:p.Ala60GlufsTer11
NM_001318012.1:c.179del NP_001304941.1:p.Ala60GlufsTer11
NM_001318013.1:c.179del NP_001304942.1:p.Ala60GlufsTer11
NM_003401.4:c.179del NP_003392.1:p.Ala60GlufsTer11
NM_022406.3:c.179del NP_071801.1:p.Ala60GlufsTer11
NM_022550.3:c.179del NP_072044.1:p.Ala60GlufsTer11
XM_017009827.2:c.179del XP_016865316.1:p.Ala60GlufsTer11
XM_017009828.2:c.179del XP_016865317.1:p.Ala60GlufsTer11
XM_017009829.2:c.179del XP_016865318.1:p.Ala60GlufsTer11
NM_001318012.2:c.179del NP_001304941.1:p.Ala60GlufsTer11
NM_001318013.2:c.179del NP_001304942.1:p.Ala60GlufsTer11
NM_003401.5:c.179del MANE Select NP_003392.1:p.Ala60GlufsTer11
NM_022406.4:c.179del NP_071801.1:p.Ala60GlufsTer11
NM_001318012.3:c.179del NP_001304941.1:p.Ala60GlufsTer11
NM_022406.5:c.179del NP_071801.1:p.Ala60GlufsTer11
NM_022550.4:c.179del NP_072044.1:p.Ala60GlufsTer11