Canonical Allele Identifier: CA649901300

Gene: XRCC4

Linked Data

• COSMIC: COSN20761256 ; COSN24139472

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83353417_83353418insC , CM000667.2:g.83353417_83353418insC	GRCh38
NC_000005.9:g.82649236_82649237insC , CM000667.1:g.82649236_82649237insC	GRCh37
NC_000005.8:g.82684992_82684993insC	NCBI36
NG_047086.1:g.281009_281010insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396027.9:c.*175_*176insC MANE Select	ENSP00000379344.4:n.*175_*176insC
ENST00000282268.7:c.*175_*176insC	ENSP00000282268.3:n.*175_*176insC
ENST00000338635.10:c.*175_*176insC	ENSP00000342011.6:n.*175_*176insC
ENST00000396027.8:c.*175_*176insC	ENSP00000379344.4:n.*175_*176insC
ENST00000511817.1:c.*175_*176insC	ENSP00000421491.1:n.*175_*176insC
NM_003401.3:c.*175_*176insC	NP_003392.1:n.*175_*176insC
NM_022406.2:c.*175_*176insC	NP_071801.1:n.*175_*176insC
NM_022550.2:c.*175_*176insC	NP_072044.1:n.*175_*176insC
XM_005248595.1:c.*175_*176insC	XP_005248652.1:n.*175_*176insC
XM_011543626.1:c.*175_*176insC	XP_011541928.1:n.*175_*176insC
XM_011543629.1:c.*175_*176insC	XP_011541931.1:n.*175_*176insC
NM_001318012.1:c.*175_*176insC	NP_001304941.1:n.*175_*176insC
NM_003401.4:c.*175_*176insC	NP_003392.1:n.*175_*176insC
NM_022406.3:c.*175_*176insC	NP_071801.1:n.*175_*176insC
NM_022550.3:c.*175_*176insC	NP_072044.1:n.*175_*176insC
XM_017009827.2:c.894-16850_894-16849insC	XP_016865316.1:n.894-16850_894-16849insC
NM_001318012.2:c.*175_*176insC	NP_001304941.1:n.*175_*176insC
NM_003401.5:c.*175_*176insC MANE Select	NP_003392.1:n.*175_*176insC
NM_022406.4:c.*175_*176insC	NP_071801.1:n.*175_*176insC
NM_001318012.3:c.*175_*176insC	NP_001304941.1:n.*175_*176insC
NM_022406.5:c.*175_*176insC	NP_071801.1:n.*175_*176insC
NM_022550.4:c.*175_*176insC	NP_072044.1:n.*175_*176insC