Canonical Allele Identifier: CA1559569136

Gene: XRCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83110989T= , CM000667.2:g.83110989T=	GRCh38
NC_000005.9:g.82406808T= , CM000667.1:g.82406808T=	GRCh37
NC_000005.8:g.82442564T=	NCBI36
NG_047086.1:g.38581T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396027.9:c.140-39T= MANE Select	ENSP00000379344.4:n.140-39T=
ENST00000282268.7:c.140-39T=	ENSP00000282268.3:n.140-39T=
ENST00000338635.10:c.140-39T=	ENSP00000342011.6:n.140-39T=
ENST00000396027.8:c.140-39T=	ENSP00000379344.4:n.140-39T=
ENST00000509268.1:n.152-39T=
ENST00000511817.1:c.140-39T=	ENSP00000421491.1:n.140-39T=
ENST00000542685.5:n.209-39T=
NM_003401.3:c.140-39T=	NP_003392.1:n.140-39T=
NM_022406.2:c.140-39T=	NP_071801.1:n.140-39T=
NM_022550.2:c.140-39T=	NP_072044.1:n.140-39T=
XM_005248595.1:c.140-39T=	XP_005248652.1:n.140-39T=
XM_011543626.1:c.140-39T=	XP_011541928.1:n.140-39T=
XM_011543627.1:c.140-39T=	XP_011541929.1:n.140-39T=
XM_011543628.1:c.140-39T=	XP_011541930.1:n.140-39T=
NM_001318012.1:c.140-39T=	NP_001304941.1:n.140-39T=
NM_001318013.1:c.140-39T=	NP_001304942.1:n.140-39T=
NM_003401.4:c.140-39T=	NP_003392.1:n.140-39T=
NM_022406.3:c.140-39T=	NP_071801.1:n.140-39T=
NM_022550.3:c.140-39T=	NP_072044.1:n.140-39T=
XM_017009827.2:c.140-39T=	XP_016865316.1:n.140-39T=
XM_017009828.2:c.140-39T=	XP_016865317.1:n.140-39T=
XM_017009829.2:c.140-39T=	XP_016865318.1:n.140-39T=
NM_001318012.2:c.140-39T=	NP_001304941.1:n.140-39T=
NM_001318013.2:c.140-39T=	NP_001304942.1:n.140-39T=
NM_003401.5:c.140-39T= MANE Select	NP_003392.1:n.140-39T=
NM_022406.4:c.140-39T=	NP_071801.1:n.140-39T=
NM_001318012.3:c.140-39T=	NP_001304941.1:n.140-39T=
NM_022406.5:c.140-39T=	NP_071801.1:n.140-39T=
NM_022550.4:c.140-39T=	NP_072044.1:n.140-39T=