Canonical Allele Identifier: CA2695200295
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 2673897
ClinVar RCV Id: RCV003450514

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58724064_58724074del , CM000679.2:g.58724064_58724074del GRCh38
NC_000017.10:g.56801425_56801435del , CM000679.1:g.56801425_56801435del GRCh37
NC_000017.9:g.54156424_54156434del NCBI36
NG_023199.1:g.36463_36473del , LRG_314:g.36463_36473del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.578_588del ENSP00000464056.2:p.Thr193AsnfsTer?
ENST00000697680.1:c.*1893_*1903del ENSP00000513392.1:n.*1893_*1903del
ENST00000697681.1:c.*2090_*2100del ENSP00000513393.1:n.*2090_*2100del
ENST00000697683.1:c.*1793_*1803del ENSP00000513395.1:n.*1793_*1803del
ENST00000697684.1:n.989_999del
ENST00000697685.1:c.*1626_*1636del ENSP00000513396.1:n.*1626_*1636del
ENST00000697686.1:c.578_588del ENSP00000513397.1:p.Thr193AsnfsTer?
ENST00000697687.1:n.808_818del
ENST00000697688.1:n.975_985del
ENST00000697689.1:c.*1440+3252_*1440+3262del ENSP00000513398.1:n.*1440+3252_*1440+3262del
ENST00000697690.1:c.904+3252_904+3262del ENSP00000513399.1:n.904+3252_904+3262del
ENST00000697691.1:c.*901_*911del ENSP00000513400.1:n.*901_*911del
ENST00000697692.1:c.*941_*951del ENSP00000513401.1:n.*941_*951del
ENST00000697694.1:c.578_588del ENSP00000513402.1:p.Thr193AsnfsTer?
ENST00000697695.1:n.1536_1546del
ENST00000337432.9:c.929_939del MANE Select ENSP00000336701.4:p.Thr310AsnfsTer?
ENST00000337432.8:c.929_939del ENSP00000336701.4:p.Thr310AsnfsTer?
ENST00000413590.5:c.567_577del
ENST00000475762.5:c.*1565_*1575del ENSP00000432421.1:n.*1565_*1575del
ENST00000482007.5:c.*357_*367del ENSP00000433332.1:n.*357_*367del
ENST00000487525.5:c.*502_*512del ENSP00000431637.1:n.*502_*512del
ENST00000578151.1:n.239+3252_239+3262del
ENST00000581221.5:n.444_454del
ENST00000583539.5:c.929_939del ENSP00000463121.1:p.Thr310AsnfsTer?
ENST00000584617.5:c.651_661del
ENST00000584804.1:c.199+3252_199+3262del ENSP00000463658.1:n.199+3252_199+3262del
NM_058216.2:c.929_939del NP_478123.1:p.Thr310AsnfsTer?
NR_103872.1:n.833_843del
XM_006722001.2:c.929_939del XP_006722064.1:p.Thr310AsnfsTer?
XM_006722002.2:c.904+3252_904+3262del XP_006722065.1:n.904+3252_904+3262del
XM_006722004.2:c.578_588del XP_006722067.1:p.Thr193AsnfsTer?
XM_006722005.2:c.578_588del XP_006722068.1:p.Thr193AsnfsTer?
XM_011525092.1:c.578_588del XP_011523394.1:p.Thr193AsnfsTer?
XM_011525093.1:c.578_588del XP_011523395.1:p.Thr193AsnfsTer?
XM_011525094.1:c.578_588del XP_011523396.1:p.Thr193AsnfsTer?
XR_934513.1:n.1147_1157del
XR_934514.1:n.1147_1157del
XM_006722001.4:c.929_939del XP_006722064.1:p.Thr310AsnfsTer?
XM_006722002.4:c.904+3252_904+3262del XP_006722065.1:n.904+3252_904+3262del
XM_006722004.3:c.578_588del XP_006722067.1:p.Thr193AsnfsTer?
XM_006722005.3:c.578_588del XP_006722068.1:p.Thr193AsnfsTer?
XM_011525092.2:c.578_588del XP_011523394.1:p.Thr193AsnfsTer?
XM_011525093.2:c.578_588del XP_011523395.1:p.Thr193AsnfsTer?
XM_011525094.2:c.578_588del XP_011523396.1:p.Thr193AsnfsTer?
XM_017024914.1:c.578_588del XP_016880403.1:p.Thr193AsnfsTer?
XM_017024915.1:c.578_588del XP_016880404.1:p.Thr193AsnfsTer?
XM_017024916.1:c.578_588del XP_016880405.1:p.Thr193AsnfsTer?
XM_017024917.1:c.578_588del XP_016880406.1:p.Thr193AsnfsTer?
XM_017024918.2:c.578_588del XP_016880407.1:p.Thr193AsnfsTer?
XM_017024919.1:c.553+3252_553+3262del XP_016880408.1:n.553+3252_553+3262del
XR_934513.3:n.1578_1588del
XR_934514.3:n.1578_1588del
NM_058216.3:c.929_939del MANE Select NP_478123.1:p.Thr310AsnfsTer?
NR_103872.2:n.804_814del