Canonical Allele Identifier: CA1559569207

Gene: XRCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83111059T= , CM000667.2:g.83111059T=	GRCh38
NC_000005.9:g.82406878T= , CM000667.1:g.82406878T=	GRCh37
NC_000005.8:g.82442634T=	NCBI36
NG_047086.1:g.38651T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396027.9:c.171T= MANE Select	ENSP00000379344.4:p.Asp57=
ENST00000282268.7:c.171T=	ENSP00000282268.3:p.Asp57=
ENST00000338635.10:c.171T=	ENSP00000342011.6:p.Asp57=
ENST00000396027.8:c.171T=	ENSP00000379344.4:p.Asp57=
ENST00000509268.1:n.183T=
ENST00000511817.1:c.171T=	ENSP00000421491.1:p.Asp57=
ENST00000542685.5:n.240T=
NM_003401.3:c.171T=	NP_003392.1:p.Asp57=
NM_022406.2:c.171T=	NP_071801.1:p.Asp57=
NM_022550.2:c.171T=	NP_072044.1:p.Asp57=
XM_005248595.1:c.171T=	XP_005248652.1:p.Asp57=
XM_011543626.1:c.171T=	XP_011541928.1:p.Asp57=
XM_011543627.1:c.171T=	XP_011541929.1:p.Asp57=
XM_011543628.1:c.171T=	XP_011541930.1:p.Asp57=
NM_001318012.1:c.171T=	NP_001304941.1:p.Asp57=
NM_001318013.1:c.171T=	NP_001304942.1:p.Asp57=
NM_003401.4:c.171T=	NP_003392.1:p.Asp57=
NM_022406.3:c.171T=	NP_071801.1:p.Asp57=
NM_022550.3:c.171T=	NP_072044.1:p.Asp57=
XM_017009827.2:c.171T=	XP_016865316.1:p.Asp57=
XM_017009828.2:c.171T=	XP_016865317.1:p.Asp57=
XM_017009829.2:c.171T=	XP_016865318.1:p.Asp57=
NM_001318012.2:c.171T=	NP_001304941.1:p.Asp57=
NM_001318013.2:c.171T=	NP_001304942.1:p.Asp57=
NM_003401.5:c.171T= MANE Select	NP_003392.1:p.Asp57=
NM_022406.4:c.171T=	NP_071801.1:p.Asp57=
NM_001318012.3:c.171T=	NP_001304941.1:p.Asp57=
NM_022406.5:c.171T=	NP_071801.1:p.Asp57=
NM_022550.4:c.171T=	NP_072044.1:p.Asp57=