Canonical Allele Identifier: CA658658636

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 484737
• ClinVar RCV Id: RCV003507291
• dbSNP Id: rs1555593498
• gnomAD v4: 17-58694971-AATT-A
• MyVariant Identifiers: chr17:g.56772335_56772337del (hg19) ; chr17:g.58694974_58694976del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58694974_58694976del , CM000679.2:g.58694974_58694976del	GRCh38
NC_000017.10:g.56772335_56772337del , CM000679.1:g.56772335_56772337del	GRCh37
NC_000017.9:g.54127334_54127336del	NCBI36
NG_023199.1:g.7373_7375del , LRG_314:g.7373_7375del
NG_047169.1:g.2106_2108del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-163_-161del	ENSP00000464056.2:n.-163_-161del
ENST00000697675.1:n.1283_1285del
ENST00000697676.1:n.249_251del
ENST00000697677.1:n.1270_1272del
ENST00000697678.1:n.91_93del
ENST00000697679.1:n.1263_1265del
ENST00000697680.1:c.*1053_*1055del	ENSP00000513392.1:n.*1053_*1055del
ENST00000697681.1:c.*1053_*1055del	ENSP00000513393.1:n.*1053_*1055del
ENST00000697683.1:c.*1053_*1055del	ENSP00000513395.1:n.*1053_*1055del
ENST00000697684.1:n.249_251del
ENST00000697685.1:c.*1053_*1055del	ENSP00000513396.1:n.*1053_*1055del
ENST00000697686.1:c.-163_-161del	ENSP00000513397.1:n.-163_-161del
ENST00000697687.1:n.235_237del
ENST00000697688.1:n.235_237del
ENST00000697689.1:c.*892_*894del	ENSP00000513398.1:n.*892_*894del
ENST00000697690.1:c.189_191del	ENSP00000513399.1:p.Ile64del
ENST00000697691.1:c.*161_*163del	ENSP00000513400.1:n.*161_*163del
ENST00000697692.1:c.*201_*203del	ENSP00000513401.1:n.*201_*203del
ENST00000697693.1:n.964_966del
ENST00000697694.1:c.-163_-161del	ENSP00000513402.1:n.-163_-161del
ENST00000697695.1:n.796_798del
ENST00000337432.9:c.189_191del MANE Select	ENSP00000336701.4:p.Ile64del
ENST00000337432.8:c.189_191del	ENSP00000336701.4:p.Ile64del
ENST00000421782.3:c.189_191del	ENSP00000391450.2:p.Ile64del
ENST00000461271.5:c.-163_-161del	ENSP00000464056.1:n.-163_-161del
ENST00000475762.5:c.*892_*894del	ENSP00000432421.1:n.*892_*894del
ENST00000482007.5:c.189_191del	ENSP00000433332.1:p.Ile64del
ENST00000486827.1:c.*1053_*1055del	ENSP00000436761.1:n.*1053_*1055del
ENST00000487525.5:c.189_191del	ENSP00000431637.1:p.Ile64del
ENST00000487921.5:n.101_103del
ENST00000583539.5:c.189_191del	ENSP00000463121.1:p.Ile64del
ENST00000584617.5:c.127-1719_127-1717del
NM_002876.3:c.189_191del	NP_002867.1:p.Ile64del
NM_058216.2:c.189_191del	NP_478123.1:p.Ile64del
NR_103872.1:n.260_262del
NR_103873.1:n.157_159del
XM_006722001.2:c.189_191del	XP_006722064.1:p.Ile64del
XM_006722002.2:c.189_191del	XP_006722065.1:p.Ile64del
XM_006722004.2:c.-163_-161del	XP_006722067.1:n.-163_-161del
XM_006722005.2:c.-163_-161del	XP_006722068.1:n.-163_-161del
XM_011525092.1:c.-163_-161del	XP_011523394.1:n.-163_-161del
XM_011525093.1:c.-163_-161del	XP_011523395.1:n.-163_-161del
XM_011525094.1:c.-163_-161del	XP_011523396.1:n.-163_-161del
XR_934513.1:n.262_264del
XR_934514.1:n.262_264del
XM_006722001.4:c.189_191del	XP_006722064.1:p.Ile64del
XM_006722002.4:c.189_191del	XP_006722065.1:p.Ile64del
XM_006722004.3:c.-163_-161del	XP_006722067.1:n.-163_-161del
XM_006722005.3:c.-163_-161del	XP_006722068.1:n.-163_-161del
XM_011525092.2:c.-163_-161del	XP_011523394.1:n.-163_-161del
XM_011525093.2:c.-163_-161del	XP_011523395.1:n.-163_-161del
XM_011525094.2:c.-163_-161del	XP_011523396.1:n.-163_-161del
XM_017024914.1:c.-163_-161del	XP_016880403.1:n.-163_-161del
XM_017024915.1:c.-163_-161del	XP_016880404.1:n.-163_-161del
XM_017024916.1:c.-163_-161del	XP_016880405.1:n.-163_-161del
XM_017024917.1:c.-163_-161del	XP_016880406.1:n.-163_-161del
XM_017024918.2:c.-163_-161del	XP_016880407.1:n.-163_-161del
XM_017024919.1:c.-163_-161del	XP_016880408.1:n.-163_-161del
XR_934513.3:n.693_695del
XR_934514.3:n.693_695del
NM_058216.3:c.189_191del MANE Select	NP_478123.1:p.Ile64del
NR_103872.2:n.231_233del
NM_002876.4:c.189_191del	NP_002867.1:p.Ile64del