Canonical Allele Identifier: CA2267814042
Gene: RAD51C HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692722_58692742delinsCTGGTGTCTGCGGGGTTCCAG , CM000679.2:g.58692722_58692742delinsCTGGTGTCTGCGGGGTTCCAG GRCh38
NC_000017.10:g.56770083_56770103delinsCTGGTGTCTGCGGGGTTCCAG , CM000679.1:g.56770083_56770103delinsCTGGTGTCTGCGGGGTTCCAG GRCh37
NC_000017.9:g.54125082_54125102delinsCTGGTGTCTGCGGGGTTCCAG NCBI36
NG_023199.1:g.5121_5141delinsCTGGTGTCTGCGGGGTTCCAG , LRG_314:g.5121_5141delinsCTGGTGTCTGCGGGGTTCCAG
NG_047169.1:g.4338_4358delinsCTGGAACCCCGCAGACACCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-207+37_-207+57delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000464056.2:n.-207+37_-207+57delinsCTGGTGTCTGCGGGGTTCCA...
ENST00000697675.1:n.150_170delinsCTGGTGTCTGCGGGGTTCCAG
ENST00000697676.1:n.139_159delinsCTGGTGTCTGCGGGGTTCCAG
ENST00000697677.1:n.137_157delinsCTGGTGTCTGCGGGGTTCCAG
ENST00000697678.1:n.47+90_47+110delinsCTGGTGTCTGCGGGGTTCCAG
ENST00000697679.1:n.130_150delinsCTGGTGTCTGCGGGGTTCCAG
ENST00000697680.1:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000513392.1:p.Leu27=
ENST00000697681.1:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000513393.1:p.Leu27=
ENST00000697683.1:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000513395.1:p.Leu27=
ENST00000697684.1:n.139_159delinsCTGGTGTCTGCGGGGTTCCAG
ENST00000697685.1:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000513396.1:p.Leu27=
ENST00000697686.1:c.-207+90_-207+110delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000513397.1:n.-207+90_-207+110delinsCTGGTGTCTGCGGGGTTCC...
ENST00000697687.1:n.125_145delinsCTGGTGTCTGCGGGGTTCCAG
ENST00000697688.1:n.125_145delinsCTGGTGTCTGCGGGGTTCCAG
ENST00000697689.1:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000513398.1:p.Leu27=
ENST00000697690.1:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000513399.1:p.Leu27=
ENST00000697691.1:c.42+37_42+57delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000513400.1:n.42+37_42+57delinsCTGGTGTCTGCGGGGTTCCAG
ENST00000697692.1:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000513401.1:p.Leu27=
ENST00000337432.9:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG MANE Select ENSP00000336701.4:p.Leu27=
ENST00000337432.8:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000336701.4:p.Leu27=
ENST00000421782.3:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000391450.2:p.Leu27=
ENST00000461271.5:c.-207+37_-207+57delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000464056.1:n.-207+37_-207+57delinsCTGGTGTCTGCGGGGTTCCA...
ENST00000475762.5:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000432421.1:p.Leu27=
ENST00000476741.2:n.121_141delinsCTGGTGTCTGCGGGGTTCCAG
ENST00000482007.5:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000433332.1:p.Leu27=
ENST00000486827.1:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000436761.1:p.Leu27=
ENST00000487525.5:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000431637.1:p.Leu27=
ENST00000487921.5:n.57+90_57+110delinsCTGGTGTCTGCGGGGTTCCAG
ENST00000583539.5:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG ENSP00000463121.1:p.Leu27=
ENST00000584617.5:c.60_80delinsCTGGTGTCTGCGGGGTTCCAG
NM_002876.3:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG NP_002867.1:p.Leu27=
NM_058216.2:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG NP_478123.1:p.Leu27=
NR_103872.1:n.150_170delinsCTGGTGTCTGCGGGGTTCCAG
NR_103873.1:n.113+37_113+57delinsCTGGTGTCTGCGGGGTTCCAG
XM_006722001.2:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG XP_006722064.1:p.Leu27=
XM_006722002.2:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG XP_006722065.1:p.Leu27=
XM_006722004.2:c.-207+37_-207+57delinsCTGGTGTCTGCGGGGTTCCAG XP_006722067.1:n.-207+37_-207+57delinsCTGGTGTCTGCGGGGTTCCAG
XM_006722005.2:c.-207+90_-207+110delinsCTGGTGTCTGCGGGGTTCCAG XP_006722068.1:n.-207+90_-207+110delinsCTGGTGTCTGCGGGGTTCCAG
XM_011525092.1:c.-507+37_-507+57delinsCTGGTGTCTGCGGGGTTCCAG XP_011523394.1:n.-507+37_-507+57delinsCTGGTGTCTGCGGGGTTCCAG
XM_011525093.1:c.-668+37_-668+57delinsCTGGTGTCTGCGGGGTTCCAG XP_011523395.1:n.-668+37_-668+57delinsCTGGTGTCTGCGGGGTTCCAG
XR_934513.1:n.152_172delinsCTGGTGTCTGCGGGGTTCCAG
XR_934514.1:n.152_172delinsCTGGTGTCTGCGGGGTTCCAG
XM_006722001.4:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG XP_006722064.1:p.Leu27=
XM_006722002.4:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG XP_006722065.1:p.Leu27=
XM_006722004.3:c.-207+37_-207+57delinsCTGGTGTCTGCGGGGTTCCAG XP_006722067.1:n.-207+37_-207+57delinsCTGGTGTCTGCGGGGTTCCAG
XM_006722005.3:c.-207+90_-207+110delinsCTGGTGTCTGCGGGGTTCCAG XP_006722068.1:n.-207+90_-207+110delinsCTGGTGTCTGCGGGGTTCCAG
XM_011525092.2:c.-507+37_-507+57delinsCTGGTGTCTGCGGGGTTCCAG XP_011523394.1:n.-507+37_-507+57delinsCTGGTGTCTGCGGGGTTCCAG
XM_011525093.2:c.-668+37_-668+57delinsCTGGTGTCTGCGGGGTTCCAG XP_011523395.1:n.-668+37_-668+57delinsCTGGTGTCTGCGGGGTTCCAG
XM_017024914.1:c.-207+37_-207+57delinsCTGGTGTCTGCGGGGTTCCAG XP_016880403.1:n.-207+37_-207+57delinsCTGGTGTCTGCGGGGTTCCAG
XM_017024916.1:c.-507+37_-507+57delinsCTGGTGTCTGCGGGGTTCCAG XP_016880405.1:n.-507+37_-507+57delinsCTGGTGTCTGCGGGGTTCCAG
XM_017024917.1:c.-207+90_-207+110delinsCTGGTGTCTGCGGGGTTCCAG XP_016880406.1:n.-207+90_-207+110delinsCTGGTGTCTGCGGGGTTCCAG
XM_017024918.2:c.-444_-424delinsCTGGTGTCTGCGGGGTTCCAG XP_016880407.1:n.-444_-424delinsCTGGTGTCTGCGGGGTTCCAG
XM_017024919.1:c.-668+37_-668+57delinsCTGGTGTCTGCGGGGTTCCAG XP_016880408.1:n.-668+37_-668+57delinsCTGGTGTCTGCGGGGTTCCAG
XR_934513.3:n.583_603delinsCTGGTGTCTGCGGGGTTCCAG
XR_934514.3:n.583_603delinsCTGGTGTCTGCGGGGTTCCAG
NM_058216.3:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG MANE Select NP_478123.1:p.Leu27=
NR_103872.2:n.121_141delinsCTGGTGTCTGCGGGGTTCCAG
NM_002876.4:c.79_99delinsCTGGTGTCTGCGGGGTTCCAG NP_002867.1:p.Leu27=
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