Canonical Allele Identifier: CA2767228158

Gene: XRCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83177810_83177811insTCT , CM000667.2:g.83177810_83177811insTCT	GRCh38
NC_000005.9:g.82473629_82473630insTCT , CM000667.1:g.82473629_82473630insTCT	GRCh37
NC_000005.8:g.82509385_82509386insTCT	NCBI36
NG_047086.1:g.105402_105403insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396027.9:c.316-17960_316-17959insTCT MANE Select	ENSP00000379344.4:n.316-17960_316-17959insTCT
ENST00000282268.7:c.316-17960_316-17959insTCT	ENSP00000282268.3:n.316-17960_316-17959insTCT
ENST00000338635.10:c.316-17960_316-17959insTCT	ENSP00000342011.6:n.316-17960_316-17959insTCT
ENST00000396027.8:c.316-17960_316-17959insTCT	ENSP00000379344.4:n.316-17960_316-17959insTCT
ENST00000509268.1:n.328-17960_328-17959insTCT
ENST00000511817.1:c.316-17960_316-17959insTCT	ENSP00000421491.1:n.316-17960_316-17959insTCT
ENST00000542685.5:n.385-17960_385-17959insTCT
NM_003401.3:c.316-17960_316-17959insTCT	NP_003392.1:n.316-17960_316-17959insTCT
NM_022406.2:c.316-17960_316-17959insTCT	NP_071801.1:n.316-17960_316-17959insTCT
NM_022550.2:c.316-17960_316-17959insTCT	NP_072044.1:n.316-17960_316-17959insTCT
XM_005248595.1:c.316-17960_316-17959insTCT	XP_005248652.1:n.316-17960_316-17959insTCT
XM_011543626.1:c.316-17960_316-17959insTCT	XP_011541928.1:n.316-17960_316-17959insTCT
XM_011543627.1:c.316-17960_316-17959insTCT	XP_011541929.1:n.316-17960_316-17959insTCT
XM_011543628.1:c.316-17960_316-17959insTCT	XP_011541930.1:n.316-17960_316-17959insTCT
NM_001318012.1:c.316-17960_316-17959insTCT	NP_001304941.1:n.316-17960_316-17959insTCT
NM_001318013.1:c.316-17960_316-17959insTCT	NP_001304942.1:n.316-17960_316-17959insTCT
NM_003401.4:c.316-17960_316-17959insTCT	NP_003392.1:n.316-17960_316-17959insTCT
NM_022406.3:c.316-17960_316-17959insTCT	NP_071801.1:n.316-17960_316-17959insTCT
NM_022550.3:c.316-17960_316-17959insTCT	NP_072044.1:n.316-17960_316-17959insTCT
XM_017009827.2:c.316-17960_316-17959insTCT	XP_016865316.1:n.316-17960_316-17959insTCT
XM_017009828.2:c.316-17960_316-17959insTCT	XP_016865317.1:n.316-17960_316-17959insTCT
XM_017009829.2:c.316-17960_316-17959insTCT	XP_016865318.1:n.316-17960_316-17959insTCT
NM_001318012.2:c.316-17960_316-17959insTCT	NP_001304941.1:n.316-17960_316-17959insTCT
NM_001318013.2:c.316-17960_316-17959insTCT	NP_001304942.1:n.316-17960_316-17959insTCT
NM_003401.5:c.316-17960_316-17959insTCT MANE Select	NP_003392.1:n.316-17960_316-17959insTCT
NM_022406.4:c.316-17960_316-17959insTCT	NP_071801.1:n.316-17960_316-17959insTCT
NM_001318012.3:c.316-17960_316-17959insTCT	NP_001304941.1:n.316-17960_316-17959insTCT
NM_022406.5:c.316-17960_316-17959insTCT	NP_071801.1:n.316-17960_316-17959insTCT
NM_022550.4:c.316-17960_316-17959insTCT	NP_072044.1:n.316-17960_316-17959insTCT