Canonical Allele Identifier: CA12150130
Gene: XRCC4 HGNC NCBI

Linked Data

dbSNP Id: rs13178127
gnomAD v2: 5-82589432-A-G
gnomAD v3: 5-83293613-A-G
gnomAD v4: 5-83293613-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83293613A>G , CM000667.2:g.83293613A>G GRCh38
NC_000005.9:g.82589432A>G , CM000667.1:g.82589432A>G GRCh37
NC_000005.8:g.82625188A>G NCBI36
NG_047086.1:g.221205A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000396027.9:c.893+34936A>G MANE Select ENSP00000379344.4:n.893+34936A>G
ENST00000282268.7:c.893+34936A>G ENSP00000282268.3:n.893+34936A>G
ENST00000338635.10:c.893+34936A>G ENSP00000342011.6:n.893+34936A>G
ENST00000396027.8:c.893+34936A>G ENSP00000379344.4:n.893+34936A>G
ENST00000511817.1:c.893+34936A>G ENSP00000421491.1:n.893+34936A>G
ENST00000542685.5:n.963-17176A>G
NM_003401.3:c.893+34936A>G NP_003392.1:n.893+34936A>G
NM_022406.2:c.893+34936A>G NP_071801.1:n.893+34936A>G
NM_022550.2:c.893+34936A>G NP_072044.1:n.893+34936A>G
XM_005248595.1:c.893+34936A>G XP_005248652.1:n.893+34936A>G
XM_011543626.1:c.893+34936A>G XP_011541928.1:n.893+34936A>G
XM_011543627.1:c.894-17176A>G XP_011541929.1:n.894-17176A>G
XM_011543629.1:c.233+34936A>G XP_011541931.1:n.233+34936A>G
NM_001318012.1:c.893+34936A>G NP_001304941.1:n.893+34936A>G
NM_001318013.1:c.894-17176A>G NP_001304942.1:n.894-17176A>G
NM_003401.4:c.893+34936A>G NP_003392.1:n.893+34936A>G
NM_022406.3:c.893+34936A>G NP_071801.1:n.893+34936A>G
NM_022550.3:c.893+34936A>G NP_072044.1:n.893+34936A>G
XM_017009827.2:c.893+34936A>G XP_016865316.1:n.893+34936A>G
NM_001318012.2:c.893+34936A>G NP_001304941.1:n.893+34936A>G
NM_001318013.2:c.894-17176A>G NP_001304942.1:n.894-17176A>G
NM_003401.5:c.893+34936A>G MANE Select NP_003392.1:n.893+34936A>G
NM_022406.4:c.893+34936A>G NP_071801.1:n.893+34936A>G
NM_001318012.3:c.893+34936A>G NP_001304941.1:n.893+34936A>G
NM_022406.5:c.893+34936A>G NP_071801.1:n.893+34936A>G
NM_022550.4:c.893+34936A>G NP_072044.1:n.893+34936A>G