Canonical Allele Identifier: CA2825002570
Community Standard Title: NM_058216.3(RAD51C):c.858_861dup (p.Thr288AspfsTer5)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720766_58720769dup , CM000679.2:g.58720766_58720769dup GRCh38
NC_000017.10:g.56798127_56798130dup , CM000679.1:g.56798127_56798130dup GRCh37
NC_000017.9:g.54153126_54153129dup NCBI36
NG_023199.1:g.33165_33168dup , LRG_314:g.33165_33168dup

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.858_861dup MANE Select NP_478123.1:p.Thr288AspfsTer5
ENST00000337432.9:c.858_861dup MANE Select ENSP00000336701.4:p.Thr288AspfsTer5
NM_058216.2:c.858_861dup NP_478123.1:p.Thr288AspfsTer5
NR_103872.1:n.762_765dup
NR_103872.2:n.733_736dup
ENST00000337432.8:c.858_861dup ENSP00000336701.4:p.Thr288AspfsTer5
ENST00000413590.5:c.496_499dup
ENST00000461271.6:c.507_510dup ENSP00000464056.2:p.Thr171AspfsTer5
ENST00000475762.5:c.*1541-3274_*1541-3271dup ENSP00000432421.1:n.*1541-3274_*1541-3271dup
ENST00000482007.5:c.*286_*289dup ENSP00000433332.1:n.*286_*289dup
ENST00000487525.5:c.*431_*434dup ENSP00000431637.1:n.*431_*434dup
ENST00000578151.1:n.193_196dup
ENST00000581221.5:n.373_376dup
ENST00000583539.5:c.858_861dup ENSP00000463121.1:p.Thr288AspfsTer5
ENST00000584617.5:c.580_583dup
ENST00000584804.1:c.153_156dup ENSP00000463658.1:p.Thr53AspfsTer5
ENST00000697678.1:n.760_763dup
ENST00000697679.1:n.1932_1935dup
ENST00000697680.1:c.*1822_*1825dup ENSP00000513392.1:n.*1822_*1825dup
ENST00000697681.1:c.*2019_*2022dup ENSP00000513393.1:n.*2019_*2022dup
ENST00000697683.1:c.*1722_*1725dup ENSP00000513395.1:n.*1722_*1725dup
ENST00000697684.1:n.918_921dup
ENST00000697685.1:c.*1555_*1558dup ENSP00000513396.1:n.*1555_*1558dup
ENST00000697686.1:c.507_510dup ENSP00000513397.1:p.Thr171AspfsTer5
ENST00000697687.1:n.737_740dup
ENST00000697688.1:n.904_907dup
ENST00000697689.1:c.*1394_*1397dup ENSP00000513398.1:n.*1394_*1397dup
ENST00000697690.1:c.858_861dup ENSP00000513399.1:p.Thr288AspfsTer5
ENST00000697691.1:c.*830_*833dup ENSP00000513400.1:n.*830_*833dup
ENST00000697692.1:c.*870_*873dup ENSP00000513401.1:n.*870_*873dup
ENST00000697694.1:c.507_510dup ENSP00000513402.1:p.Thr171AspfsTer5
ENST00000697695.1:n.1465_1468dup
XM_006722001.2:c.858_861dup XP_006722064.1:p.Thr288AspfsTer5
XM_006722001.4:c.858_861dup XP_006722064.1:p.Thr288AspfsTer5
XM_006722002.2:c.858_861dup XP_006722065.1:p.Thr288AspfsTer5
XM_006722002.4:c.858_861dup XP_006722065.1:p.Thr288AspfsTer5
XM_006722004.2:c.507_510dup XP_006722067.1:p.Thr171AspfsTer5
XM_006722004.3:c.507_510dup XP_006722067.1:p.Thr171AspfsTer5
XM_006722005.2:c.507_510dup XP_006722068.1:p.Thr171AspfsTer5
XM_006722005.3:c.507_510dup XP_006722068.1:p.Thr171AspfsTer5
XM_011525092.1:c.507_510dup XP_011523394.1:p.Thr171AspfsTer5
XM_011525092.2:c.507_510dup XP_011523394.1:p.Thr171AspfsTer5
XM_011525093.1:c.507_510dup XP_011523395.1:p.Thr171AspfsTer5
XM_011525093.2:c.507_510dup XP_011523395.1:p.Thr171AspfsTer5
XM_011525094.1:c.507_510dup XP_011523396.1:p.Thr171AspfsTer5
XM_011525094.2:c.507_510dup XP_011523396.1:p.Thr171AspfsTer5
XM_017024914.1:c.507_510dup XP_016880403.1:p.Thr171AspfsTer5
XM_017024915.1:c.507_510dup XP_016880404.1:p.Thr171AspfsTer5
XM_017024916.1:c.507_510dup XP_016880405.1:p.Thr171AspfsTer5
XM_017024917.1:c.507_510dup XP_016880406.1:p.Thr171AspfsTer5
XM_017024918.2:c.507_510dup XP_016880407.1:p.Thr171AspfsTer5
XM_017024919.1:c.507_510dup XP_016880408.1:p.Thr171AspfsTer5
XR_934513.1:n.1076_1079dup
XR_934513.3:n.1507_1510dup
XR_934514.1:n.1076_1079dup
XR_934514.3:n.1507_1510dup