Canonical Allele Identifier: CA1559694002

Gene: XRCC4

Linked Data

• dbSNP Id: rs1757125608
• gnomAD v4: 5-83353067-TTCTTTTACTCTATAAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83353068_83353083del , CM000667.2:g.83353068_83353083del	GRCh38
NC_000005.9:g.82648887_82648902del , CM000667.1:g.82648887_82648902del	GRCh37
NC_000005.8:g.82684643_82684658del	NCBI36
NG_047086.1:g.280660_280675del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396027.9:c.894-63_894-48del MANE Select	ENSP00000379344.4:n.894-63_894-48del
ENST00000282268.7:c.894-63_894-48del	ENSP00000282268.3:n.894-63_894-48del
ENST00000338635.10:c.894-57_894-42del	ENSP00000342011.6:n.894-57_894-42del
ENST00000396027.8:c.894-63_894-48del	ENSP00000379344.4:n.894-63_894-48del
ENST00000511817.1:c.894-57_894-42del	ENSP00000421491.1:n.894-57_894-42del
NM_003401.3:c.894-63_894-48del	NP_003392.1:n.894-63_894-48del
NM_022406.2:c.894-57_894-42del	NP_071801.1:n.894-57_894-42del
NM_022550.2:c.894-63_894-48del	NP_072044.1:n.894-63_894-48del
XM_005248595.1:c.894-57_894-42del	XP_005248652.1:n.894-57_894-42del
XM_011543626.1:c.894-57_894-42del	XP_011541928.1:n.894-57_894-42del
XM_011543629.1:c.234-57_234-42del	XP_011541931.1:n.234-57_234-42del
NM_001318012.1:c.894-57_894-42del	NP_001304941.1:n.894-57_894-42del
NM_003401.4:c.894-63_894-48del	NP_003392.1:n.894-63_894-48del
NM_022406.3:c.894-57_894-42del	NP_071801.1:n.894-57_894-42del
NM_022550.3:c.894-63_894-48del	NP_072044.1:n.894-63_894-48del
XM_017009827.2:c.894-17199_894-17184del	XP_016865316.1:n.894-17199_894-17184del
NM_001318012.2:c.894-57_894-42del	NP_001304941.1:n.894-57_894-42del
NM_003401.5:c.894-63_894-48del MANE Select	NP_003392.1:n.894-63_894-48del
NM_022406.4:c.894-57_894-42del	NP_071801.1:n.894-57_894-42del
NM_001318012.3:c.894-57_894-42del	NP_001304941.1:n.894-57_894-42del
NM_022406.5:c.894-57_894-42del	NP_071801.1:n.894-57_894-42del
NM_022550.4:c.894-63_894-48del	NP_072044.1:n.894-63_894-48del