Canonical Allele Identifier: CA3261180593
Community Standard Title: NM_058216.3(RAD51C):c.1093_1095delinsCCT (p.Thr365Pro)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734184_58734186delinsCCT , CM000679.2:g.58734184_58734186delinsCCT GRCh38
NC_000017.10:g.56811545_56811547delinsCCT , CM000679.1:g.56811545_56811547delinsCCT GRCh37
NC_000017.9:g.54166544_54166546delinsCCT NCBI36
NG_023199.1:g.46583_46585delinsCCT , LRG_314:g.46583_46585delinsCCT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1093_1095delinsCCT MANE Select NP_478123.1:p.Thr365Pro
ENST00000337432.9:c.1093_1095delinsCCT MANE Select ENSP00000336701.4:p.Thr365Pro
NM_058216.2:c.1093_1095delinsCCT NP_478123.1:p.Thr365Pro
NR_103872.1:n.997_999delinsCCT
NR_103872.2:n.968_970delinsCCT
ENST00000337432.8:c.1093_1095delinsCCT ENSP00000336701.4:p.Thr365Pro
ENST00000413590.5:c.734_736delinsCCT
ENST00000461271.6:c.*1625_*1627delinsCCT ENSP00000464056.2:n.*1625_*1627delinsCCT
ENST00000461706.1:n.280_282delinsCCT
ENST00000475762.5:c.*1729_*1731delinsCCT ENSP00000432421.1:n.*1729_*1731delinsCCT
ENST00000482007.5:c.*521_*523delinsCCT ENSP00000433332.1:n.*521_*523delinsCCT
ENST00000487525.5:c.*669_*671delinsCCT ENSP00000431637.1:n.*669_*671delinsCCT
ENST00000578151.1:n.306_308delinsCCT
ENST00000581221.5:n.608_610delinsCCT
ENST00000584804.1:c.327_329delinsCCT ENSP00000463658.1:n.327_329delinsCCT
ENST00000697680.1:c.*2057_*2059delinsCCT ENSP00000513392.1:n.*2057_*2059delinsCCT
ENST00000697681.1:c.*2254_*2256delinsCCT ENSP00000513393.1:n.*2254_*2256delinsCCT
ENST00000697683.1:c.*2029_*2031delinsCCT ENSP00000513395.1:n.*2029_*2031delinsCCT
ENST00000697685.1:c.*1790_*1792delinsCCT ENSP00000513396.1:n.*1790_*1792delinsCCT
ENST00000697686.1:c.*3_*5delinsCCT ENSP00000513397.1:n.*3_*5delinsCCT
ENST00000697689.1:c.*1507_*1509delinsCCT ENSP00000513398.1:n.*1507_*1509delinsCCT
ENST00000697690.1:c.*53_*55delinsCCT ENSP00000513399.1:n.*53_*55delinsCCT
ENST00000697691.1:c.*1065_*1067delinsCCT ENSP00000513400.1:n.*1065_*1067delinsCCT
ENST00000697692.1:c.*1105_*1107delinsCCT ENSP00000513401.1:n.*1105_*1107delinsCCT
ENST00000697694.1:c.742_744delinsCCT ENSP00000513402.1:p.Thr248Pro
ENST00000697695.1:n.1700_1702delinsCCT
XM_006722001.2:c.1096_1098delinsCCT XP_006722064.1:p.Thr366Pro
XM_006722001.4:c.1096_1098delinsCCT XP_006722064.1:p.Thr366Pro
XM_006722002.2:c.*3_*5delinsCCT XP_006722065.1:n.*3_*5delinsCCT
XM_006722002.4:c.*3_*5delinsCCT XP_006722065.1:n.*3_*5delinsCCT
XM_006722004.2:c.745_747delinsCCT XP_006722067.1:p.Thr249Pro
XM_006722004.3:c.745_747delinsCCT XP_006722067.1:p.Thr249Pro
XM_006722005.2:c.745_747delinsCCT XP_006722068.1:p.Thr249Pro
XM_006722005.3:c.745_747delinsCCT XP_006722068.1:p.Thr249Pro
XM_011525092.1:c.745_747delinsCCT XP_011523394.1:p.Thr249Pro
XM_011525092.2:c.745_747delinsCCT XP_011523394.1:p.Thr249Pro
XM_011525093.1:c.745_747delinsCCT XP_011523395.1:p.Thr249Pro
XM_011525093.2:c.745_747delinsCCT XP_011523395.1:p.Thr249Pro
XM_011525094.1:c.745_747delinsCCT XP_011523396.1:p.Thr249Pro
XM_011525094.2:c.745_747delinsCCT XP_011523396.1:p.Thr249Pro
XM_017024914.1:c.742_744delinsCCT XP_016880403.1:p.Thr248Pro
XM_017024915.1:c.742_744delinsCCT XP_016880404.1:p.Thr248Pro
XM_017024916.1:c.742_744delinsCCT XP_016880405.1:p.Thr248Pro
XM_017024917.1:c.742_744delinsCCT XP_016880406.1:p.Thr248Pro
XM_017024918.2:c.742_744delinsCCT XP_016880407.1:p.Thr248Pro
XM_017024919.1:c.*3_*5delinsCCT XP_016880408.1:n.*3_*5delinsCCT
XR_934513.1:n.1311_1313delinsCCT
XR_934513.3:n.1742_1744delinsCCT
XR_934886.1:n.149+3885_149+3887delinsAGG
XR_934886.2:n.149+3885_149+3887delinsAGG