Canonical Allele Identifier: CA560925104

Gene: XRCC4

Linked Data

• dbSNP Id: rs1314900752
• gnomAD v2: 5-82451037-CTCATA-C
• gnomAD v3: 5-83155218-CTCATA-C
• gnomAD v4: 5-83155218-CTCATA-C
• MyVariant Identifiers: chr5:g.82451038_82451042del (hg19) ; chr5:g.83155219_83155223del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83155223_83155227del , CM000667.2:g.83155223_83155227del	GRCh38
NC_000005.9:g.82451042_82451046del , CM000667.1:g.82451042_82451046del	GRCh37
NC_000005.8:g.82486798_82486802del	NCBI36
NG_047086.1:g.82815_82819del

Transcript Alleles

HGVS	Amino-acid change
ENST00000396027.9:c.316-40547_316-40543del MANE Select	ENSP00000379344.4:n.316-40547_316-40543de...
ENST00000282268.7:c.316-40547_316-40543del	ENSP00000282268.3:n.316-40547_316-40543de...
ENST00000338635.10:c.316-40547_316-40543del	ENSP00000342011.6:n.316-40547_316-40543de...
ENST00000396027.8:c.316-40547_316-40543del	ENSP00000379344.4:n.316-40547_316-40543de...
ENST00000509268.1:n.328-40547_328-40543del
ENST00000511817.1:c.316-40547_316-40543del	ENSP00000421491.1:n.316-40547_316-40543de...
ENST00000542685.5:n.385-40547_385-40543del
NM_003401.3:c.316-40547_316-40543del	NP_003392.1:n.316-40547_316-40543del
NM_022406.2:c.316-40547_316-40543del	NP_071801.1:n.316-40547_316-40543del
NM_022550.2:c.316-40547_316-40543del	NP_072044.1:n.316-40547_316-40543del
XM_005248595.1:c.316-40547_316-40543del	XP_005248652.1:n.316-40547_316-40543del
XM_011543626.1:c.316-40547_316-40543del	XP_011541928.1:n.316-40547_316-40543del
XM_011543627.1:c.316-40547_316-40543del	XP_011541929.1:n.316-40547_316-40543del
XM_011543628.1:c.316-40547_316-40543del	XP_011541930.1:n.316-40547_316-40543del
NM_001318012.1:c.316-40547_316-40543del	NP_001304941.1:n.316-40547_316-40543del
NM_001318013.1:c.316-40547_316-40543del	NP_001304942.1:n.316-40547_316-40543del
NM_003401.4:c.316-40547_316-40543del	NP_003392.1:n.316-40547_316-40543del
NM_022406.3:c.316-40547_316-40543del	NP_071801.1:n.316-40547_316-40543del
NM_022550.3:c.316-40547_316-40543del	NP_072044.1:n.316-40547_316-40543del
XM_017009827.2:c.316-40547_316-40543del	XP_016865316.1:n.316-40547_316-40543del
XM_017009828.2:c.316-40547_316-40543del	XP_016865317.1:n.316-40547_316-40543del
XM_017009829.2:c.316-40547_316-40543del	XP_016865318.1:n.316-40547_316-40543del
NM_001318012.2:c.316-40547_316-40543del	NP_001304941.1:n.316-40547_316-40543del
NM_001318013.2:c.316-40547_316-40543del	NP_001304942.1:n.316-40547_316-40543del
NM_003401.5:c.316-40547_316-40543del MANE Select	NP_003392.1:n.316-40547_316-40543del
NM_022406.4:c.316-40547_316-40543del	NP_071801.1:n.316-40547_316-40543del
NM_001318012.3:c.316-40547_316-40543del	NP_001304941.1:n.316-40547_316-40543del
NM_022406.5:c.316-40547_316-40543del	NP_071801.1:n.316-40547_316-40543del
NM_022550.4:c.316-40547_316-40543del	NP_072044.1:n.316-40547_316-40543del