Canonical Allele Identifier: CA3057243383
Community Standard Title: NM_058216.3(RAD51C):c.1076_1078del (p.Thr359_Glu360delinsLys)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734167_58734169del , CM000679.2:g.58734167_58734169del GRCh38
NC_000017.10:g.56811528_56811530del , CM000679.1:g.56811528_56811530del GRCh37
NC_000017.9:g.54166527_54166529del NCBI36
NG_023199.1:g.46566_46568del , LRG_314:g.46566_46568del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1076_1078del MANE Select NP_478123.1:p.Thr359_Glu360delinsLys
ENST00000337432.9:c.1076_1078del MANE Select ENSP00000336701.4:p.Thr359_Glu360delinsLys
NM_058216.2:c.1076_1078del NP_478123.1:p.Thr359_Glu360delinsLys
NR_103872.1:n.980_982del
NR_103872.2:n.951_953del
ENST00000337432.8:c.1076_1078del ENSP00000336701.4:p.Thr359_Glu360delinsLys
ENST00000413590.5:c.717_719del
ENST00000461271.6:c.*1608_*1610del ENSP00000464056.2:n.*1608_*1610del
ENST00000461706.1:n.263_265del
ENST00000475762.5:c.*1712_*1714del ENSP00000432421.1:n.*1712_*1714del
ENST00000482007.5:c.*504_*506del ENSP00000433332.1:n.*504_*506del
ENST00000487525.5:c.*652_*654del ENSP00000431637.1:n.*652_*654del
ENST00000578151.1:n.289_291del
ENST00000581221.5:n.591_593del
ENST00000584804.1:c.310_312del ENSP00000463658.1:p.Gln104del
ENST00000697680.1:c.*2040_*2042del ENSP00000513392.1:n.*2040_*2042del
ENST00000697681.1:c.*2237_*2239del ENSP00000513393.1:n.*2237_*2239del
ENST00000697683.1:c.*2012_*2014del ENSP00000513395.1:n.*2012_*2014del
ENST00000697685.1:c.*1773_*1775del ENSP00000513396.1:n.*1773_*1775del
ENST00000697686.1:c.847_849del ENSP00000513397.1:p.Gln283del
ENST00000697689.1:c.*1490_*1492del ENSP00000513398.1:n.*1490_*1492del
ENST00000697690.1:c.*36_*38del ENSP00000513399.1:n.*36_*38del
ENST00000697691.1:c.*1048_*1050del ENSP00000513400.1:n.*1048_*1050del
ENST00000697692.1:c.*1088_*1090del ENSP00000513401.1:n.*1088_*1090del
ENST00000697694.1:c.725_727del ENSP00000513402.1:p.Thr242_Glu243delinsLys
ENST00000697695.1:n.1683_1685del
XM_006722001.2:c.1079_1081del XP_006722064.1:p.Thr360_Glu361delinsLys
XM_006722001.4:c.1079_1081del XP_006722064.1:p.Thr360_Glu361delinsLys
XM_006722002.2:c.1015_1017del XP_006722065.1:p.Gln339del
XM_006722002.4:c.1015_1017del XP_006722065.1:p.Gln339del
XM_006722004.2:c.728_730del XP_006722067.1:p.Thr243_Glu244delinsLys
XM_006722004.3:c.728_730del XP_006722067.1:p.Thr243_Glu244delinsLys
XM_006722005.2:c.728_730del XP_006722068.1:p.Thr243_Glu244delinsLys
XM_006722005.3:c.728_730del XP_006722068.1:p.Thr243_Glu244delinsLys
XM_011525092.1:c.728_730del XP_011523394.1:p.Thr243_Glu244delinsLys
XM_011525092.2:c.728_730del XP_011523394.1:p.Thr243_Glu244delinsLys
XM_011525093.1:c.728_730del XP_011523395.1:p.Thr243_Glu244delinsLys
XM_011525093.2:c.728_730del XP_011523395.1:p.Thr243_Glu244delinsLys
XM_011525094.1:c.728_730del XP_011523396.1:p.Thr243_Glu244delinsLys
XM_011525094.2:c.728_730del XP_011523396.1:p.Thr243_Glu244delinsLys
XM_017024914.1:c.725_727del XP_016880403.1:p.Thr242_Glu243delinsLys
XM_017024915.1:c.725_727del XP_016880404.1:p.Thr242_Glu243delinsLys
XM_017024916.1:c.725_727del XP_016880405.1:p.Thr242_Glu243delinsLys
XM_017024917.1:c.725_727del XP_016880406.1:p.Thr242_Glu243delinsLys
XM_017024918.2:c.725_727del XP_016880407.1:p.Thr242_Glu243delinsLys
XM_017024919.1:c.664_666del XP_016880408.1:p.Gln222del
XR_934513.1:n.1294_1296del
XR_934513.3:n.1725_1727del
XR_934514.1:n.1297_1299del
XR_934514.3:n.1728_1730del
XR_934886.1:n.149+3902_149+3904del
XR_934886.2:n.149+3902_149+3904del