Canonical Allele Identifier: CA1559694253

Gene: XRCC4

Linked Data

• dbSNP Id: rs1176304411

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83353253_83353255del , CM000667.2:g.83353253_83353255del	GRCh38
NC_000005.9:g.82649072_82649074del , CM000667.1:g.82649072_82649074del	GRCh37
NC_000005.8:g.82684828_82684830del	NCBI36
NG_047086.1:g.280845_280847del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396027.9:c.*11_*13del MANE Select	ENSP00000379344.4:n.*11_*13del
ENST00000282268.7:c.*11_*13del	ENSP00000282268.3:n.*11_*13del
ENST00000338635.10:c.*11_*13del	ENSP00000342011.6:n.*11_*13del
ENST00000396027.8:c.*11_*13del	ENSP00000379344.4:n.*11_*13del
ENST00000511817.1:c.*11_*13del	ENSP00000421491.1:n.*11_*13del
NM_003401.3:c.*11_*13del	NP_003392.1:n.*11_*13del
NM_022406.2:c.*11_*13del	NP_071801.1:n.*11_*13del
NM_022550.2:c.*11_*13del	NP_072044.1:n.*11_*13del
XM_005248595.1:c.*11_*13del	XP_005248652.1:n.*11_*13del
XM_011543626.1:c.*11_*13del	XP_011541928.1:n.*11_*13del
XM_011543629.1:c.*11_*13del	XP_011541931.1:n.*11_*13del
NM_001318012.1:c.*11_*13del	NP_001304941.1:n.*11_*13del
NM_003401.4:c.*11_*13del	NP_003392.1:n.*11_*13del
NM_022406.3:c.*11_*13del	NP_071801.1:n.*11_*13del
NM_022550.3:c.*11_*13del	NP_072044.1:n.*11_*13del
XM_017009827.2:c.894-17014_894-17012del	XP_016865316.1:n.894-17014_894-17012del
NM_001318012.2:c.*11_*13del	NP_001304941.1:n.*11_*13del
NM_003401.5:c.*11_*13del MANE Select	NP_003392.1:n.*11_*13del
NM_022406.4:c.*11_*13del	NP_071801.1:n.*11_*13del
NM_001318012.3:c.*11_*13del	NP_001304941.1:n.*11_*13del
NM_022406.5:c.*11_*13del	NP_071801.1:n.*11_*13del
NM_022550.4:c.*11_*13del	NP_072044.1:n.*11_*13del