Canonical Allele Identifier: CA1559687106

Gene: XRCC4

Linked Data

• dbSNP Id: rs7734849

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83344130T>G , CM000667.2:g.83344130T>G	GRCh38
NC_000005.9:g.82639949T>G , CM000667.1:g.82639949T>G	GRCh37
NC_000005.8:g.82675705T>G	NCBI36
NG_047086.1:g.271722T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396027.9:c.894-9001T>G MANE Select	ENSP00000379344.4:n.894-9001T>G
ENST00000282268.7:c.894-9001T>G	ENSP00000282268.3:n.894-9001T>G
ENST00000338635.10:c.894-8995T>G	ENSP00000342011.6:n.894-8995T>G
ENST00000396027.8:c.894-9001T>G	ENSP00000379344.4:n.894-9001T>G
ENST00000511817.1:c.894-8995T>G	ENSP00000421491.1:n.894-8995T>G
NM_003401.3:c.894-9001T>G	NP_003392.1:n.894-9001T>G
NM_022406.2:c.894-8995T>G	NP_071801.1:n.894-8995T>G
NM_022550.2:c.894-9001T>G	NP_072044.1:n.894-9001T>G
XM_005248595.1:c.894-8995T>G	XP_005248652.1:n.894-8995T>G
XM_011543626.1:c.894-8995T>G	XP_011541928.1:n.894-8995T>G
XM_011543629.1:c.234-8995T>G	XP_011541931.1:n.234-8995T>G
NM_001318012.1:c.894-8995T>G	NP_001304941.1:n.894-8995T>G
NM_003401.4:c.894-9001T>G	NP_003392.1:n.894-9001T>G
NM_022406.3:c.894-8995T>G	NP_071801.1:n.894-8995T>G
NM_022550.3:c.894-9001T>G	NP_072044.1:n.894-9001T>G
XM_017009827.2:c.894-26137T>G	XP_016865316.1:n.894-26137T>G
NM_001318012.2:c.894-8995T>G	NP_001304941.1:n.894-8995T>G
NM_003401.5:c.894-9001T>G MANE Select	NP_003392.1:n.894-9001T>G
NM_022406.4:c.894-8995T>G	NP_071801.1:n.894-8995T>G
NM_001318012.3:c.894-8995T>G	NP_001304941.1:n.894-8995T>G
NM_022406.5:c.894-8995T>G	NP_071801.1:n.894-8995T>G
NM_022550.4:c.894-9001T>G	NP_072044.1:n.894-9001T>G