Canonical Allele Identifier: CA1559694047
Gene: XRCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83353127C= , CM000667.2:g.83353127C= GRCh38
NC_000005.9:g.82648946C= , CM000667.1:g.82648946C= GRCh37
NC_000005.8:g.82684702C= NCBI36
NG_047086.1:g.280719C=

Transcript Alleles

HGVS Amino-acid change
ENST00000396027.9:c.894-4C= MANE Select ENSP00000379344.4:n.894-4C=
ENST00000282268.7:c.894-4C= ENSP00000282268.3:n.894-4C=
ENST00000338635.10:c.896C= ENSP00000342011.6:p.Ser299=
ENST00000396027.8:c.894-4C= ENSP00000379344.4:n.894-4C=
ENST00000511817.1:c.896C= ENSP00000421491.1:p.Ser299=
NM_003401.3:c.894-4C= NP_003392.1:n.894-4C=
NM_022406.2:c.896C= NP_071801.1:p.Ser299=
NM_022550.2:c.894-4C= NP_072044.1:n.894-4C=
XM_005248595.1:c.896C= XP_005248652.1:p.Ser299=
XM_011543626.1:c.896C= XP_011541928.1:p.Ser299=
XM_011543629.1:c.236C= XP_011541931.1:p.Ser79=
NM_001318012.1:c.896C= NP_001304941.1:p.Ser299=
NM_003401.4:c.894-4C= NP_003392.1:n.894-4C=
NM_022406.3:c.896C= NP_071801.1:p.Ser299=
NM_022550.3:c.894-4C= NP_072044.1:n.894-4C=
XM_017009827.2:c.894-17140C= XP_016865316.1:n.894-17140C=
NM_001318012.2:c.896C= NP_001304941.1:p.Ser299=
NM_003401.5:c.894-4C= MANE Select NP_003392.1:n.894-4C=
NM_022406.4:c.896C= NP_071801.1:p.Ser299=
NM_001318012.3:c.896C= NP_001304941.1:p.Ser299=
NM_022406.5:c.896C= NP_071801.1:p.Ser299=
NM_022550.4:c.894-4C= NP_072044.1:n.894-4C=