Canonical Allele Identifier: CA3057229300
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695182_58695184del , CM000679.2:g.58695182_58695184del GRCh38
NC_000017.10:g.56772543_56772545del , CM000679.1:g.56772543_56772545del GRCh37
NC_000017.9:g.54127542_54127544del NCBI36
NG_023199.1:g.7581_7583del , LRG_314:g.7581_7583del
NG_047169.1:g.1897_1899del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.46_48del ENSP00000464056.2:p.Gln16del
ENST00000697675.1:n.1491_1493del
ENST00000697676.1:n.457_459del
ENST00000697677.1:n.1478_1480del
ENST00000697678.1:n.299_301del
ENST00000697679.1:n.1471_1473del
ENST00000697680.1:c.*1261_*1263del ENSP00000513392.1:n.*1261_*1263del
ENST00000697681.1:c.*1261_*1263del ENSP00000513393.1:n.*1261_*1263del
ENST00000697683.1:c.*1261_*1263del ENSP00000513395.1:n.*1261_*1263del
ENST00000697684.1:n.457_459del
ENST00000697685.1:c.*1261_*1263del ENSP00000513396.1:n.*1261_*1263del
ENST00000697686.1:c.46_48del ENSP00000513397.1:p.Gln16del
ENST00000697687.1:n.443_445del
ENST00000697688.1:n.443_445del
ENST00000697689.1:c.*1100_*1102del ENSP00000513398.1:n.*1100_*1102del
ENST00000697690.1:c.397_399del ENSP00000513399.1:p.Gln133del
ENST00000697691.1:c.*369_*371del ENSP00000513400.1:n.*369_*371del
ENST00000697692.1:c.*409_*411del ENSP00000513401.1:n.*409_*411del
ENST00000697693.1:n.1172_1174del
ENST00000697694.1:c.46_48del ENSP00000513402.1:p.Gln16del
ENST00000697695.1:n.1004_1006del
ENST00000337432.9:c.397_399del MANE Select ENSP00000336701.4:p.Gln133del
ENST00000337432.8:c.397_399del ENSP00000336701.4:p.Gln133del
ENST00000413590.5:c.35_37del
ENST00000421782.3:c.397_399del ENSP00000391450.2:p.Gln133del
ENST00000425173.5:c.193_195del ENSP00000407282.1:p.Gln65del
ENST00000461271.5:c.46_48del ENSP00000464056.1:p.Gln16del
ENST00000475762.5:c.*1100_*1102del ENSP00000432421.1:n.*1100_*1102del
ENST00000482007.5:c.397_399del ENSP00000433332.1:p.Gln133del
ENST00000486827.1:c.*1261_*1263del ENSP00000436761.1:n.*1261_*1263del
ENST00000487525.5:c.397_399del ENSP00000431637.1:p.Gln133del
ENST00000487921.5:n.309_311del
ENST00000583539.5:c.397_399del ENSP00000463121.1:p.Gln133del
ENST00000584617.5:c.127-1511_127-1509del
ENST00000622327.4:c.133_135del ENSP00000482326.1:p.Gln45del
NM_002876.3:c.397_399del NP_002867.1:p.Gln133del
NM_058216.2:c.397_399del NP_478123.1:p.Gln133del
NR_103872.1:n.468_470del
NR_103873.1:n.365_367del
XM_006722001.2:c.397_399del XP_006722064.1:p.Gln133del
XM_006722002.2:c.397_399del XP_006722065.1:p.Gln133del
XM_006722004.2:c.46_48del XP_006722067.1:p.Gln16del
XM_006722005.2:c.46_48del XP_006722068.1:p.Gln16del
XM_011525092.1:c.46_48del XP_011523394.1:p.Gln16del
XM_011525093.1:c.46_48del XP_011523395.1:p.Gln16del
XM_011525094.1:c.46_48del XP_011523396.1:p.Gln16del
XR_934513.1:n.470_472del
XR_934514.1:n.470_472del
XM_006722001.4:c.397_399del XP_006722064.1:p.Gln133del
XM_006722002.4:c.397_399del XP_006722065.1:p.Gln133del
XM_006722004.3:c.46_48del XP_006722067.1:p.Gln16del
XM_006722005.3:c.46_48del XP_006722068.1:p.Gln16del
XM_011525092.2:c.46_48del XP_011523394.1:p.Gln16del
XM_011525093.2:c.46_48del XP_011523395.1:p.Gln16del
XM_011525094.2:c.46_48del XP_011523396.1:p.Gln16del
XM_017024914.1:c.46_48del XP_016880403.1:p.Gln16del
XM_017024915.1:c.46_48del XP_016880404.1:p.Gln16del
XM_017024916.1:c.46_48del XP_016880405.1:p.Gln16del
XM_017024917.1:c.46_48del XP_016880406.1:p.Gln16del
XM_017024918.2:c.46_48del XP_016880407.1:p.Gln16del
XM_017024919.1:c.46_48del XP_016880408.1:p.Gln16del
XR_934513.3:n.901_903del
XR_934514.3:n.901_903del
NM_058216.3:c.397_399del MANE Select NP_478123.1:p.Gln133del
NR_103872.2:n.439_441del
NM_002876.4:c.397_399del NP_002867.1:p.Gln133del