Canonical Allele Identifier: CA1559592435
Gene: XRCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83155187G= , CM000667.2:g.83155187G= GRCh38
NC_000005.9:g.82451006G= , CM000667.1:g.82451006G= GRCh37
NC_000005.8:g.82486762G= NCBI36
NG_047086.1:g.82779G=

Transcript Alleles

HGVS Amino-acid change
ENST00000396027.9:c.316-40583G= MANE Select ENSP00000379344.4:n.316-40583G=
ENST00000282268.7:c.316-40583G= ENSP00000282268.3:n.316-40583G=
ENST00000338635.10:c.316-40583G= ENSP00000342011.6:n.316-40583G=
ENST00000396027.8:c.316-40583G= ENSP00000379344.4:n.316-40583G=
ENST00000509268.1:n.328-40583G=
ENST00000511817.1:c.316-40583G= ENSP00000421491.1:n.316-40583G=
ENST00000542685.5:n.385-40583G=
NM_003401.3:c.316-40583G= NP_003392.1:n.316-40583G=
NM_022406.2:c.316-40583G= NP_071801.1:n.316-40583G=
NM_022550.2:c.316-40583G= NP_072044.1:n.316-40583G=
XM_005248595.1:c.316-40583G= XP_005248652.1:n.316-40583G=
XM_011543626.1:c.316-40583G= XP_011541928.1:n.316-40583G=
XM_011543627.1:c.316-40583G= XP_011541929.1:n.316-40583G=
XM_011543628.1:c.316-40583G= XP_011541930.1:n.316-40583G=
NM_001318012.1:c.316-40583G= NP_001304941.1:n.316-40583G=
NM_001318013.1:c.316-40583G= NP_001304942.1:n.316-40583G=
NM_003401.4:c.316-40583G= NP_003392.1:n.316-40583G=
NM_022406.3:c.316-40583G= NP_071801.1:n.316-40583G=
NM_022550.3:c.316-40583G= NP_072044.1:n.316-40583G=
XM_017009827.2:c.316-40583G= XP_016865316.1:n.316-40583G=
XM_017009828.2:c.316-40583G= XP_016865317.1:n.316-40583G=
XM_017009829.2:c.316-40583G= XP_016865318.1:n.316-40583G=
NM_001318012.2:c.316-40583G= NP_001304941.1:n.316-40583G=
NM_001318013.2:c.316-40583G= NP_001304942.1:n.316-40583G=
NM_003401.5:c.316-40583G= MANE Select NP_003392.1:n.316-40583G=
NM_022406.4:c.316-40583G= NP_071801.1:n.316-40583G=
NM_001318012.3:c.316-40583G= NP_001304941.1:n.316-40583G=
NM_022406.5:c.316-40583G= NP_071801.1:n.316-40583G=
NM_022550.4:c.316-40583G= NP_072044.1:n.316-40583G=