Canonical Allele Identifier: CA1559694090

Gene: XRCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83353155G= , CM000667.2:g.83353155G=	GRCh38
NC_000005.9:g.82648974G= , CM000667.1:g.82648974G=	GRCh37
NC_000005.8:g.82684730G=	NCBI36
NG_047086.1:g.280747G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396027.9:c.918G= MANE Select	ENSP00000379344.4:p.Thr306=
ENST00000282268.7:c.918G=	ENSP00000282268.3:p.Thr306=
ENST00000338635.10:c.924G=	ENSP00000342011.6:p.Thr308=
ENST00000396027.8:c.918G=	ENSP00000379344.4:p.Thr306=
ENST00000511817.1:c.924G=	ENSP00000421491.1:p.Thr308=
NM_003401.3:c.918G=	NP_003392.1:p.Thr306=
NM_022406.2:c.924G=	NP_071801.1:p.Thr308=
NM_022550.2:c.918G=	NP_072044.1:p.Thr306=
XM_005248595.1:c.924G=	XP_005248652.1:p.Thr308=
XM_011543626.1:c.924G=	XP_011541928.1:p.Thr308=
XM_011543629.1:c.264G=	XP_011541931.1:p.Thr88=
NM_001318012.1:c.924G=	NP_001304941.1:p.Thr308=
NM_003401.4:c.918G=	NP_003392.1:p.Thr306=
NM_022406.3:c.924G=	NP_071801.1:p.Thr308=
NM_022550.3:c.918G=	NP_072044.1:p.Thr306=
XM_017009827.2:c.894-17112G=	XP_016865316.1:n.894-17112G=
NM_001318012.2:c.924G=	NP_001304941.1:p.Thr308=
NM_003401.5:c.918G= MANE Select	NP_003392.1:p.Thr306=
NM_022406.4:c.924G=	NP_071801.1:p.Thr308=
NM_001318012.3:c.924G=	NP_001304941.1:p.Thr308=
NM_022406.5:c.924G=	NP_071801.1:p.Thr308=
NM_022550.4:c.918G=	NP_072044.1:p.Thr306=