Canonical Allele Identifier: CA445279297

Gene: XRCC4

Linked Data

• MyVariant Identifiers: chr5:g.82649028C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83353209C>T , CM000667.2:g.83353209C>T	GRCh38
NC_000005.9:g.82649028C>T , CM000667.1:g.82649028C>T	GRCh37
NC_000005.8:g.82684784C>T	NCBI36
NG_047086.1:g.280801C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396027.9:c.972C>T MANE Select	ENSP00000379344.4:p.Asn324=
ENST00000282268.7:c.972C>T	ENSP00000282268.3:p.Asn324=
ENST00000338635.10:c.978C>T	ENSP00000342011.6:p.Asn326=
ENST00000396027.8:c.972C>T	ENSP00000379344.4:p.Asn324=
ENST00000511817.1:c.978C>T	ENSP00000421491.1:p.Asn326=
NM_003401.3:c.972C>T	NP_003392.1:p.Asn324=
NM_022406.2:c.978C>T	NP_071801.1:p.Asn326=
NM_022550.2:c.972C>T	NP_072044.1:p.Asn324=
XM_005248595.1:c.978C>T	XP_005248652.1:p.Asn326=
XM_011543626.1:c.978C>T	XP_011541928.1:p.Asn326=
XM_011543629.1:c.318C>T	XP_011541931.1:p.Asn106=
NM_001318012.1:c.978C>T	NP_001304941.1:p.Asn326=
NM_003401.4:c.972C>T	NP_003392.1:p.Asn324=
NM_022406.3:c.978C>T	NP_071801.1:p.Asn326=
NM_022550.3:c.972C>T	NP_072044.1:p.Asn324=
XM_017009827.2:c.894-17058C>T	XP_016865316.1:n.894-17058C>T
NM_001318012.2:c.978C>T	NP_001304941.1:p.Asn326=
NM_003401.5:c.972C>T MANE Select	NP_003392.1:p.Asn324=
NM_022406.4:c.978C>T	NP_071801.1:p.Asn326=
NM_001318012.3:c.978C>T	NP_001304941.1:p.Asn326=
NM_022406.5:c.978C>T	NP_071801.1:p.Asn326=
NM_022550.4:c.972C>T	NP_072044.1:p.Asn324=