Canonical Allele Identifier: CA1559694439
Gene: XRCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83353452A= , CM000667.2:g.83353452A= GRCh38
NC_000005.9:g.82649271A= , CM000667.1:g.82649271A= GRCh37
NC_000005.8:g.82685027A= NCBI36
NG_047086.1:g.281044A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396027.9:c.*210A= MANE Select ENSP00000379344.4:n.*210A=
ENST00000282268.7:c.*210A= ENSP00000282268.3:n.*210A=
ENST00000338635.10:c.*210A= ENSP00000342011.6:n.*210A=
ENST00000396027.8:c.*210A= ENSP00000379344.4:n.*210A=
ENST00000511817.1:c.*210A= ENSP00000421491.1:n.*210A=
NM_003401.3:c.*210A= NP_003392.1:n.*210A=
NM_022406.2:c.*210A= NP_071801.1:n.*210A=
NM_022550.2:c.*210A= NP_072044.1:n.*210A=
XM_005248595.1:c.*210A= XP_005248652.1:n.*210A=
XM_011543626.1:c.*210A= XP_011541928.1:n.*210A=
XM_011543629.1:c.*210A= XP_011541931.1:n.*210A=
NM_001318012.1:c.*210A= NP_001304941.1:n.*210A=
NM_003401.4:c.*210A= NP_003392.1:n.*210A=
NM_022406.3:c.*210A= NP_071801.1:n.*210A=
NM_022550.3:c.*210A= NP_072044.1:n.*210A=
XM_017009827.2:c.894-16815A= XP_016865316.1:n.894-16815A=
NM_001318012.2:c.*210A= NP_001304941.1:n.*210A=
NM_003401.5:c.*210A= MANE Select NP_003392.1:n.*210A=
NM_022406.4:c.*210A= NP_071801.1:n.*210A=
NM_001318012.3:c.*210A= NP_001304941.1:n.*210A=
NM_022406.5:c.*210A= NP_071801.1:n.*210A=
NM_022550.4:c.*210A= NP_072044.1:n.*210A=