Canonical Allele Identifier: CA1078152716

Gene: XRCC4

Linked Data

• dbSNP Id: rs1748901634
• gnomAD v3: 5-83155220-CATATCATGAGTGTAT-C
• gnomAD v4: 5-83155220-CATATCATGAGTGTAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83155223_83155237del , CM000667.2:g.83155223_83155237del	GRCh38
NC_000005.9:g.82451042_82451056del , CM000667.1:g.82451042_82451056del	GRCh37
NC_000005.8:g.82486798_82486812del	NCBI36
NG_047086.1:g.82815_82829del

Transcript Alleles

HGVS	Amino-acid change
ENST00000396027.9:c.316-40547_316-40533del MANE Select	ENSP00000379344.4:n.316-40547_316-40533de...
ENST00000282268.7:c.316-40547_316-40533del	ENSP00000282268.3:n.316-40547_316-40533de...
ENST00000338635.10:c.316-40547_316-40533del	ENSP00000342011.6:n.316-40547_316-40533de...
ENST00000396027.8:c.316-40547_316-40533del	ENSP00000379344.4:n.316-40547_316-40533de...
ENST00000509268.1:n.328-40547_328-40533del
ENST00000511817.1:c.316-40547_316-40533del	ENSP00000421491.1:n.316-40547_316-40533de...
ENST00000542685.5:n.385-40547_385-40533del
NM_003401.3:c.316-40547_316-40533del	NP_003392.1:n.316-40547_316-40533del
NM_022406.2:c.316-40547_316-40533del	NP_071801.1:n.316-40547_316-40533del
NM_022550.2:c.316-40547_316-40533del	NP_072044.1:n.316-40547_316-40533del
XM_005248595.1:c.316-40547_316-40533del	XP_005248652.1:n.316-40547_316-40533del
XM_011543626.1:c.316-40547_316-40533del	XP_011541928.1:n.316-40547_316-40533del
XM_011543627.1:c.316-40547_316-40533del	XP_011541929.1:n.316-40547_316-40533del
XM_011543628.1:c.316-40547_316-40533del	XP_011541930.1:n.316-40547_316-40533del
NM_001318012.1:c.316-40547_316-40533del	NP_001304941.1:n.316-40547_316-40533del
NM_001318013.1:c.316-40547_316-40533del	NP_001304942.1:n.316-40547_316-40533del
NM_003401.4:c.316-40547_316-40533del	NP_003392.1:n.316-40547_316-40533del
NM_022406.3:c.316-40547_316-40533del	NP_071801.1:n.316-40547_316-40533del
NM_022550.3:c.316-40547_316-40533del	NP_072044.1:n.316-40547_316-40533del
XM_017009827.2:c.316-40547_316-40533del	XP_016865316.1:n.316-40547_316-40533del
XM_017009828.2:c.316-40547_316-40533del	XP_016865317.1:n.316-40547_316-40533del
XM_017009829.2:c.316-40547_316-40533del	XP_016865318.1:n.316-40547_316-40533del
NM_001318012.2:c.316-40547_316-40533del	NP_001304941.1:n.316-40547_316-40533del
NM_001318013.2:c.316-40547_316-40533del	NP_001304942.1:n.316-40547_316-40533del
NM_003401.5:c.316-40547_316-40533del MANE Select	NP_003392.1:n.316-40547_316-40533del
NM_022406.4:c.316-40547_316-40533del	NP_071801.1:n.316-40547_316-40533del
NM_001318012.3:c.316-40547_316-40533del	NP_001304941.1:n.316-40547_316-40533del
NM_022406.5:c.316-40547_316-40533del	NP_071801.1:n.316-40547_316-40533del
NM_022550.4:c.316-40547_316-40533del	NP_072044.1:n.316-40547_316-40533del