Canonical Allele Identifier: CA1559694282

Gene: XRCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83353268C= , CM000667.2:g.83353268C=	GRCh38
NC_000005.9:g.82649087C= , CM000667.1:g.82649087C=	GRCh37
NC_000005.8:g.82684843C=	NCBI36
NG_047086.1:g.280860C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396027.9:c.*26C= MANE Select	ENSP00000379344.4:n.*26C=
ENST00000282268.7:c.*26C=	ENSP00000282268.3:n.*26C=
ENST00000338635.10:c.*26C=	ENSP00000342011.6:n.*26C=
ENST00000396027.8:c.*26C=	ENSP00000379344.4:n.*26C=
ENST00000511817.1:c.*26C=	ENSP00000421491.1:n.*26C=
NM_003401.3:c.*26C=	NP_003392.1:n.*26C=
NM_022406.2:c.*26C=	NP_071801.1:n.*26C=
NM_022550.2:c.*26C=	NP_072044.1:n.*26C=
XM_005248595.1:c.*26C=	XP_005248652.1:n.*26C=
XM_011543626.1:c.*26C=	XP_011541928.1:n.*26C=
XM_011543629.1:c.*26C=	XP_011541931.1:n.*26C=
NM_001318012.1:c.*26C=	NP_001304941.1:n.*26C=
NM_003401.4:c.*26C=	NP_003392.1:n.*26C=
NM_022406.3:c.*26C=	NP_071801.1:n.*26C=
NM_022550.3:c.*26C=	NP_072044.1:n.*26C=
XM_017009827.2:c.894-16999C=	XP_016865316.1:n.894-16999C=
NM_001318012.2:c.*26C=	NP_001304941.1:n.*26C=
NM_003401.5:c.*26C= MANE Select	NP_003392.1:n.*26C=
NM_022406.4:c.*26C=	NP_071801.1:n.*26C=
NM_001318012.3:c.*26C=	NP_001304941.1:n.*26C=
NM_022406.5:c.*26C=	NP_071801.1:n.*26C=
NM_022550.4:c.*26C=	NP_072044.1:n.*26C=