Canonical Allele Identifier: CA360357590

Gene: XRCC4

Linked Data

• MyVariant Identifiers: chr5:g.82648948A>T (hg19) ; chr5:g.83353129A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83353129A>T , CM000667.2:g.83353129A>T	GRCh38
NC_000005.9:g.82648948A>T , CM000667.1:g.82648948A>T	GRCh37
NC_000005.8:g.82684704A>T	NCBI36
NG_047086.1:g.280721A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396027.9:c.894-2A>T MANE Select	ENSP00000379344.4:n.894-2A>T
ENST00000282268.7:c.894-2A>T	ENSP00000282268.3:n.894-2A>T
ENST00000338635.10:c.898A>T	ENSP00000342011.6:p.Arg300Trp
ENST00000396027.8:c.894-2A>T	ENSP00000379344.4:n.894-2A>T
ENST00000511817.1:c.898A>T	ENSP00000421491.1:p.Arg300Trp
NM_003401.3:c.894-2A>T	NP_003392.1:n.894-2A>T
NM_022406.2:c.898A>T	NP_071801.1:p.Arg300Trp
NM_022550.2:c.894-2A>T	NP_072044.1:n.894-2A>T
XM_005248595.1:c.898A>T	XP_005248652.1:p.Arg300Trp
XM_011543626.1:c.898A>T	XP_011541928.1:p.Arg300Trp
XM_011543629.1:c.238A>T	XP_011541931.1:p.Arg80Trp
NM_001318012.1:c.898A>T	NP_001304941.1:p.Arg300Trp
NM_003401.4:c.894-2A>T	NP_003392.1:n.894-2A>T
NM_022406.3:c.898A>T	NP_071801.1:p.Arg300Trp
NM_022550.3:c.894-2A>T	NP_072044.1:n.894-2A>T
XM_017009827.2:c.894-17138A>T	XP_016865316.1:n.894-17138A>T
NM_001318012.2:c.898A>T	NP_001304941.1:p.Arg300Trp
NM_003401.5:c.894-2A>T MANE Select	NP_003392.1:n.894-2A>T
NM_022406.4:c.898A>T	NP_071801.1:p.Arg300Trp
NM_001318012.3:c.898A>T	NP_001304941.1:p.Arg300Trp
NM_022406.5:c.898A>T	NP_071801.1:p.Arg300Trp
NM_022550.4:c.894-2A>T	NP_072044.1:n.894-2A>T