Canonical Allele Identifier: CA2160435585
Community Standard Title: NM_005432.4(XRCC3):c.561+1132G=

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.103702041C= , CM000676.2:g.103702041C= GRCh38
NC_000014.8:g.104168378C= , CM000676.1:g.104168378C= GRCh37
NC_000014.7:g.103238131C= NCBI36
NG_011516.1:g.18446G=
NG_012307.1:g.77854C=

Transcript Alleles

HGVS Amino-acid Change
NM_005432.4:c.561+1132G= (XRCC3) MANE Select NP_005423.1:n.561+1132G=
ENST00000555055.6:c.561+1132G= (XRCC3) MANE Select ENSP00000452598.1:n.561+1132G=
NM_001100118.1:c.561+1132G= (XRCC3) NP_001093588.1:n.561+1132G=
NM_001100118.2:c.561+1132G= (XRCC3) NP_001093588.1:n.561+1132G=
NM_001100119.1:c.561+1132G= (XRCC3) NP_001093589.1:n.561+1132G=
NM_001100119.2:c.561+1132G= (XRCC3) NP_001093589.1:n.561+1132G=
NM_001371229.1:c.561+1132G= (XRCC3) NP_001358158.1:n.561+1132G=
NM_001371231.1:c.561+1132G= (XRCC3) NP_001358160.1:n.561+1132G=
NM_001371232.1:c.561+1132G= (XRCC3) NP_001358161.1:n.561+1132G=
NM_005432.3:c.561+1132G= (XRCC3) NP_005423.1:n.561+1132G=
ENST00000348520.10:c.*842C= (KLC1) ENSP00000341154.6:n.*842C=
ENST00000352127.11:c.561+1132G= (XRCC3) ENSP00000343392.7:n.561+1132G=
ENST00000553264.5:c.561+1132G= (XRCC3) ENSP00000451974.1:n.561+1132G=
ENST00000554774.1:n.175+1132G= (XRCC3)
ENST00000554811.5:n.2008+1132G= (XRCC3)
ENST00000554913.5:c.561+1132G= (XRCC3) ENSP00000451362.1:n.561+1132G=
ENST00000554974.5:c.-54-2465G= (XRCC3) ENSP00000451361.1:n.-54-2465G=
ENST00000555055.5:c.561+1132G= (XRCC3) ENSP00000452598.1:n.561+1132G=
ENST00000555451.1:n.155+1132G= (XRCC3)
ENST00000555832.1:n.607G= (XRCC3)
XM_005268046.1:c.561+1132G= (XRCC3) XP_005268103.1:n.561+1132G=
XM_005268046.2:c.561+1132G= (XRCC3) XP_005268103.1:n.561+1132G=
XM_011537138.1:c.561+1132G= (XRCC3) XP_011535440.1:n.561+1132G=
XM_011537138.2:c.561+1132G= (XRCC3) XP_011535440.1:n.561+1132G=
XM_024449799.1:c.109C= XP_024305567.1:p.Arg37=
XM_024449800.1:c.-91C= XP_024305568.1:n.-91C=
XR_002957600.1:n.226C=