Canonical Allele Identifier: CA560933602

Gene: XRCC4

Linked Data

• dbSNP Id: rs1204115885
• gnomAD v2: 5-82589482-ATCAGTTTGTAAATT-A
• gnomAD v3: 5-83293663-ATCAGTTTGTAAATT-A
• gnomAD v4: 5-83293663-ATCAGTTTGTAAATT-A
• MyVariant Identifiers: chr5:g.82589483_82589496del (hg19) ; chr5:g.83293664_83293677del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83293668_83293681del , CM000667.2:g.83293668_83293681del	GRCh38
NC_000005.9:g.82589487_82589500del , CM000667.1:g.82589487_82589500del	GRCh37
NC_000005.8:g.82625243_82625256del	NCBI36
NG_047086.1:g.221260_221273del

Transcript Alleles

HGVS	Amino-acid change
ENST00000396027.9:c.893+34991_893+35004del MANE Select	ENSP00000379344.4:n.893+34991_893+35004de...
ENST00000282268.7:c.893+34991_893+35004del	ENSP00000282268.3:n.893+34991_893+35004de...
ENST00000338635.10:c.893+34991_893+35004del	ENSP00000342011.6:n.893+34991_893+35004de...
ENST00000396027.8:c.893+34991_893+35004del	ENSP00000379344.4:n.893+34991_893+35004de...
ENST00000511817.1:c.893+34991_893+35004del	ENSP00000421491.1:n.893+34991_893+35004de...
ENST00000542685.5:n.963-17121_963-17108del
NM_003401.3:c.893+34991_893+35004del	NP_003392.1:n.893+34991_893+35004del
NM_022406.2:c.893+34991_893+35004del	NP_071801.1:n.893+34991_893+35004del
NM_022550.2:c.893+34991_893+35004del	NP_072044.1:n.893+34991_893+35004del
XM_005248595.1:c.893+34991_893+35004del	XP_005248652.1:n.893+34991_893+35004del
XM_011543626.1:c.893+34991_893+35004del	XP_011541928.1:n.893+34991_893+35004del
XM_011543627.1:c.894-17121_894-17108del	XP_011541929.1:n.894-17121_894-17108del
XM_011543629.1:c.233+34991_233+35004del	XP_011541931.1:n.233+34991_233+35004del
NM_001318012.1:c.893+34991_893+35004del	NP_001304941.1:n.893+34991_893+35004del
NM_001318013.1:c.894-17121_894-17108del	NP_001304942.1:n.894-17121_894-17108del
NM_003401.4:c.893+34991_893+35004del	NP_003392.1:n.893+34991_893+35004del
NM_022406.3:c.893+34991_893+35004del	NP_071801.1:n.893+34991_893+35004del
NM_022550.3:c.893+34991_893+35004del	NP_072044.1:n.893+34991_893+35004del
XM_017009827.2:c.893+34991_893+35004del	XP_016865316.1:n.893+34991_893+35004del
NM_001318012.2:c.893+34991_893+35004del	NP_001304941.1:n.893+34991_893+35004del
NM_001318013.2:c.894-17121_894-17108del	NP_001304942.1:n.894-17121_894-17108del
NM_003401.5:c.893+34991_893+35004del MANE Select	NP_003392.1:n.893+34991_893+35004del
NM_022406.4:c.893+34991_893+35004del	NP_071801.1:n.893+34991_893+35004del
NM_001318012.3:c.893+34991_893+35004del	NP_001304941.1:n.893+34991_893+35004del
NM_022406.5:c.893+34991_893+35004del	NP_071801.1:n.893+34991_893+35004del
NM_022550.4:c.893+34991_893+35004del	NP_072044.1:n.893+34991_893+35004del