Canonical Allele Identifier: CA122023085

Gene: XRCC4

Linked Data

• dbSNP Id: rs1022237088
• MyVariant Identifiers: chr5:g.82589498C>T (hg19) ; chr5:g.83293679C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83293679C>T , CM000667.2:g.83293679C>T	GRCh38
NC_000005.9:g.82589498C>T , CM000667.1:g.82589498C>T	GRCh37
NC_000005.8:g.82625254C>T	NCBI36
NG_047086.1:g.221271C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396027.9:c.893+35002C>T MANE Select	ENSP00000379344.4:n.893+35002C>T
ENST00000282268.7:c.893+35002C>T	ENSP00000282268.3:n.893+35002C>T
ENST00000338635.10:c.893+35002C>T	ENSP00000342011.6:n.893+35002C>T
ENST00000396027.8:c.893+35002C>T	ENSP00000379344.4:n.893+35002C>T
ENST00000511817.1:c.893+35002C>T	ENSP00000421491.1:n.893+35002C>T
ENST00000542685.5:n.963-17110C>T
NM_003401.3:c.893+35002C>T	NP_003392.1:n.893+35002C>T
NM_022406.2:c.893+35002C>T	NP_071801.1:n.893+35002C>T
NM_022550.2:c.893+35002C>T	NP_072044.1:n.893+35002C>T
XM_005248595.1:c.893+35002C>T	XP_005248652.1:n.893+35002C>T
XM_011543626.1:c.893+35002C>T	XP_011541928.1:n.893+35002C>T
XM_011543627.1:c.894-17110C>T	XP_011541929.1:n.894-17110C>T
XM_011543629.1:c.233+35002C>T	XP_011541931.1:n.233+35002C>T
NM_001318012.1:c.893+35002C>T	NP_001304941.1:n.893+35002C>T
NM_001318013.1:c.894-17110C>T	NP_001304942.1:n.894-17110C>T
NM_003401.4:c.893+35002C>T	NP_003392.1:n.893+35002C>T
NM_022406.3:c.893+35002C>T	NP_071801.1:n.893+35002C>T
NM_022550.3:c.893+35002C>T	NP_072044.1:n.893+35002C>T
XM_017009827.2:c.893+35002C>T	XP_016865316.1:n.893+35002C>T
NM_001318012.2:c.893+35002C>T	NP_001304941.1:n.893+35002C>T
NM_001318013.2:c.894-17110C>T	NP_001304942.1:n.894-17110C>T
NM_003401.5:c.893+35002C>T MANE Select	NP_003392.1:n.893+35002C>T
NM_022406.4:c.893+35002C>T	NP_071801.1:n.893+35002C>T
NM_001318012.3:c.893+35002C>T	NP_001304941.1:n.893+35002C>T
NM_022406.5:c.893+35002C>T	NP_071801.1:n.893+35002C>T
NM_022550.4:c.893+35002C>T	NP_072044.1:n.893+35002C>T