Canonical Allele Identifier: CA1559569132
Gene: XRCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83110985C= , CM000667.2:g.83110985C= GRCh38
NC_000005.9:g.82406804C= , CM000667.1:g.82406804C= GRCh37
NC_000005.8:g.82442560C= NCBI36
NG_047086.1:g.38577C=

Transcript Alleles

HGVS Amino-acid change
ENST00000396027.9:c.140-43C= MANE Select ENSP00000379344.4:n.140-43C=
ENST00000282268.7:c.140-43C= ENSP00000282268.3:n.140-43C=
ENST00000338635.10:c.140-43C= ENSP00000342011.6:n.140-43C=
ENST00000396027.8:c.140-43C= ENSP00000379344.4:n.140-43C=
ENST00000509268.1:n.152-43C=
ENST00000511817.1:c.140-43C= ENSP00000421491.1:n.140-43C=
ENST00000542685.5:n.209-43C=
NM_003401.3:c.140-43C= NP_003392.1:n.140-43C=
NM_022406.2:c.140-43C= NP_071801.1:n.140-43C=
NM_022550.2:c.140-43C= NP_072044.1:n.140-43C=
XM_005248595.1:c.140-43C= XP_005248652.1:n.140-43C=
XM_011543626.1:c.140-43C= XP_011541928.1:n.140-43C=
XM_011543627.1:c.140-43C= XP_011541929.1:n.140-43C=
XM_011543628.1:c.140-43C= XP_011541930.1:n.140-43C=
NM_001318012.1:c.140-43C= NP_001304941.1:n.140-43C=
NM_001318013.1:c.140-43C= NP_001304942.1:n.140-43C=
NM_003401.4:c.140-43C= NP_003392.1:n.140-43C=
NM_022406.3:c.140-43C= NP_071801.1:n.140-43C=
NM_022550.3:c.140-43C= NP_072044.1:n.140-43C=
XM_017009827.2:c.140-43C= XP_016865316.1:n.140-43C=
XM_017009828.2:c.140-43C= XP_016865317.1:n.140-43C=
XM_017009829.2:c.140-43C= XP_016865318.1:n.140-43C=
NM_001318012.2:c.140-43C= NP_001304941.1:n.140-43C=
NM_001318013.2:c.140-43C= NP_001304942.1:n.140-43C=
NM_003401.5:c.140-43C= MANE Select NP_003392.1:n.140-43C=
NM_022406.4:c.140-43C= NP_071801.1:n.140-43C=
NM_001318012.3:c.140-43C= NP_001304941.1:n.140-43C=
NM_022406.5:c.140-43C= NP_071801.1:n.140-43C=
NM_022550.4:c.140-43C= NP_072044.1:n.140-43C=