Canonical Allele Identifier: CA3261180159
Community Standard Title: NM_058216.3(RAD51C):c.107_108delinsTC (p.Glu36Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692750_58692751delinsTC , CM000679.2:g.58692750_58692751delinsTC GRCh38
NC_000017.10:g.56770111_56770112delinsTC , CM000679.1:g.56770111_56770112delinsTC GRCh37
NC_000017.9:g.54125110_54125111delinsTC NCBI36
NG_023199.1:g.5149_5150delinsTC , LRG_314:g.5149_5150delinsTC
NG_047169.1:g.4329_4330delinsGA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.107_108delinsTC MANE Select NP_478123.1:p.Glu36Val
ENST00000337432.9:c.107_108delinsTC MANE Select ENSP00000336701.4:p.Glu36Val
NM_002876.3:c.107_108delinsTC NP_002867.1:p.Glu36Val
NM_002876.4:c.107_108delinsTC NP_002867.1:p.Glu36Val
NM_058216.2:c.107_108delinsTC NP_478123.1:p.Glu36Val
NR_103872.1:n.178_179delinsTC
NR_103872.2:n.149_150delinsTC
NR_103873.1:n.113+65_113+66delinsTC
ENST00000337432.8:c.107_108delinsTC ENSP00000336701.4:p.Glu36Val
ENST00000421782.3:c.107_108delinsTC ENSP00000391450.2:p.Glu36Val
ENST00000461271.5:c.-207+65_-207+66delinsTC ENSP00000464056.1:n.-207+65_-207+66delinsTC
ENST00000461271.6:c.-207+65_-207+66delinsTC ENSP00000464056.2:n.-207+65_-207+66delinsTC
ENST00000475762.5:c.107_108delinsTC ENSP00000432421.1:p.Glu36Val
ENST00000476741.2:n.149_150delinsTC
ENST00000482007.5:c.107_108delinsTC ENSP00000433332.1:p.Glu36Val
ENST00000486827.1:c.107_108delinsTC ENSP00000436761.1:p.Glu36Val
ENST00000487525.5:c.107_108delinsTC ENSP00000431637.1:p.Glu36Val
ENST00000487921.5:n.57+118_57+119delinsTC
ENST00000583539.5:c.107_108delinsTC ENSP00000463121.1:p.Glu36Val
ENST00000584617.5:c.88_89delinsTC
ENST00000697675.1:n.178_179delinsTC
ENST00000697676.1:n.167_168delinsTC
ENST00000697677.1:n.165_166delinsTC
ENST00000697678.1:n.47+118_47+119delinsTC
ENST00000697679.1:n.158_159delinsTC
ENST00000697680.1:c.107_108delinsTC ENSP00000513392.1:p.Glu36Val
ENST00000697681.1:c.107_108delinsTC ENSP00000513393.1:p.Glu36Val
ENST00000697683.1:c.107_108delinsTC ENSP00000513395.1:p.Glu36Val
ENST00000697684.1:n.167_168delinsTC
ENST00000697685.1:c.107_108delinsTC ENSP00000513396.1:p.Glu36Val
ENST00000697686.1:c.-207+118_-207+119delinsTC ENSP00000513397.1:n.-207+118_-207+119delinsTC
ENST00000697687.1:n.153_154delinsTC
ENST00000697688.1:n.153_154delinsTC
ENST00000697689.1:c.107_108delinsTC ENSP00000513398.1:p.Glu36Val
ENST00000697690.1:c.107_108delinsTC ENSP00000513399.1:p.Glu36Val
ENST00000697691.1:c.42+65_42+66delinsTC ENSP00000513400.1:n.42+65_42+66delinsTC
ENST00000697692.1:c.107_108delinsTC ENSP00000513401.1:p.Glu36Val
ENST00000697693.1:n.20_21delinsTC
XM_006722001.2:c.107_108delinsTC XP_006722064.1:p.Glu36Val
XM_006722001.4:c.107_108delinsTC XP_006722064.1:p.Glu36Val
XM_006722002.2:c.107_108delinsTC XP_006722065.1:p.Glu36Val
XM_006722002.4:c.107_108delinsTC XP_006722065.1:p.Glu36Val
XM_006722004.2:c.-207+65_-207+66delinsTC XP_006722067.1:n.-207+65_-207+66delinsTC
XM_006722004.3:c.-207+65_-207+66delinsTC XP_006722067.1:n.-207+65_-207+66delinsTC
XM_006722005.2:c.-207+118_-207+119delinsTC XP_006722068.1:n.-207+118_-207+119delinsTC
XM_006722005.3:c.-207+118_-207+119delinsTC XP_006722068.1:n.-207+118_-207+119delinsTC
XM_011525092.1:c.-507+65_-507+66delinsTC XP_011523394.1:n.-507+65_-507+66delinsTC
XM_011525092.2:c.-507+65_-507+66delinsTC XP_011523394.1:n.-507+65_-507+66delinsTC
XM_011525093.1:c.-668+65_-668+66delinsTC XP_011523395.1:n.-668+65_-668+66delinsTC
XM_011525093.2:c.-668+65_-668+66delinsTC XP_011523395.1:n.-668+65_-668+66delinsTC
XM_017024914.1:c.-207+65_-207+66delinsTC XP_016880403.1:n.-207+65_-207+66delinsTC
XM_017024916.1:c.-507+65_-507+66delinsTC XP_016880405.1:n.-507+65_-507+66delinsTC
XM_017024917.1:c.-207+118_-207+119delinsTC XP_016880406.1:n.-207+118_-207+119delinsTC
XM_017024918.2:c.-416_-415delinsTC XP_016880407.1:n.-416_-415delinsTC
XM_017024919.1:c.-668+65_-668+66delinsTC XP_016880408.1:n.-668+65_-668+66delinsTC
XR_934513.1:n.180_181delinsTC
XR_934513.3:n.611_612delinsTC
XR_934514.1:n.180_181delinsTC
XR_934514.3:n.611_612delinsTC