Canonical Allele Identifier: CA773573792

Gene: RAD51C

Linked Data

• dbSNP Id: rs1328168814
• gnomAD v4: 17-58696598-CTTTAGT-C
• MyVariant Identifiers: chr17:g.56773960_56773965del (hg19) ; chr17:g.58696599_58696604del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696599_58696604del , CM000679.2:g.58696599_58696604del	GRCh38
NC_000017.10:g.56773960_56773965del , CM000679.1:g.56773960_56773965del	GRCh37
NC_000017.9:g.54128959_54128964del	NCBI36
NG_023199.1:g.8998_9003del , LRG_314:g.8998_9003del
NG_047169.1:g.476_481del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.54-94_54-89del	ENSP00000464056.2:n.54-94_54-89del
ENST00000697675.1:n.2908_2913del
ENST00000697676.1:n.465-94_465-89del
ENST00000697677.1:n.1486-94_1486-89del
ENST00000697678.1:n.307-94_307-89del
ENST00000697679.1:n.1479-94_1479-89del
ENST00000697680.1:c.*1269-94_*1269-89del	ENSP00000513392.1:n.*1269-94_*1269-89del
ENST00000697681.1:c.*1296-94_*1296-89del	ENSP00000513393.1:n.*1296-94_*1296-89del
ENST00000697683.1:c.*1269-94_*1269-89del	ENSP00000513395.1:n.*1269-94_*1269-89del
ENST00000697684.1:n.465-94_465-89del
ENST00000697685.1:c.*1268+1410_*1268+1415del	ENSP00000513396.1:n.*1268+1410_*1268+1415...
ENST00000697686.1:c.54-94_54-89del	ENSP00000513397.1:n.54-94_54-89del
ENST00000697687.1:n.450+1410_450+1415del
ENST00000697688.1:n.451-94_451-89del
ENST00000697689.1:c.*1107+1410_*1107+1415del	ENSP00000513398.1:n.*1107+1410_*1107+1415...
ENST00000697690.1:c.405-94_405-89del	ENSP00000513399.1:n.405-94_405-89del
ENST00000697691.1:c.*377-94_*377-89del	ENSP00000513400.1:n.*377-94_*377-89del
ENST00000697692.1:c.*417-94_*417-89del	ENSP00000513401.1:n.*417-94_*417-89del
ENST00000697694.1:c.54-94_54-89del	ENSP00000513402.1:n.54-94_54-89del
ENST00000697695.1:n.1012-94_1012-89del
ENST00000337432.9:c.405-94_405-89del MANE Select	ENSP00000336701.4:n.405-94_405-89del
ENST00000337432.8:c.405-94_405-89del	ENSP00000336701.4:n.405-94_405-89del
ENST00000413590.5:c.43-94_43-89del
ENST00000425173.5:c.201-94_201-89del	ENSP00000407282.1:n.201-94_201-89del
ENST00000461271.5:c.54-94_54-89del	ENSP00000464056.1:n.54-94_54-89del
ENST00000475762.5:c.*1108-94_*1108-89del	ENSP00000432421.1:n.*1108-94_*1108-89del
ENST00000482007.5:c.404+1410_404+1415del	ENSP00000433332.1:n.404+1410_404+1415del
ENST00000487525.5:c.404+1410_404+1415del	ENSP00000431637.1:n.404+1410_404+1415del
ENST00000487921.5:n.317-94_317-89del
ENST00000583539.5:c.405-94_405-89del	ENSP00000463121.1:n.405-94_405-89del
ENST00000584617.5:c.127-94_127-89del
ENST00000622327.4:c.141-94_141-89del	ENSP00000482326.1:n.141-94_141-89del
NM_058216.2:c.405-94_405-89del	NP_478123.1:n.405-94_405-89del
NR_103872.1:n.475+1410_475+1415del
XM_006722001.2:c.405-94_405-89del	XP_006722064.1:n.405-94_405-89del
XM_006722002.2:c.405-94_405-89del	XP_006722065.1:n.405-94_405-89del
XM_006722004.2:c.54-94_54-89del	XP_006722067.1:n.54-94_54-89del
XM_006722005.2:c.54-94_54-89del	XP_006722068.1:n.54-94_54-89del
XM_011525092.1:c.54-94_54-89del	XP_011523394.1:n.54-94_54-89del
XM_011525093.1:c.54-94_54-89del	XP_011523395.1:n.54-94_54-89del
XM_011525094.1:c.54-94_54-89del	XP_011523396.1:n.54-94_54-89del
XR_934513.1:n.478-94_478-89del
XR_934514.1:n.478-94_478-89del
XM_006722001.4:c.405-94_405-89del	XP_006722064.1:n.405-94_405-89del
XM_006722002.4:c.405-94_405-89del	XP_006722065.1:n.405-94_405-89del
XM_006722004.3:c.54-94_54-89del	XP_006722067.1:n.54-94_54-89del
XM_006722005.3:c.54-94_54-89del	XP_006722068.1:n.54-94_54-89del
XM_011525092.2:c.54-94_54-89del	XP_011523394.1:n.54-94_54-89del
XM_011525093.2:c.54-94_54-89del	XP_011523395.1:n.54-94_54-89del
XM_011525094.2:c.54-94_54-89del	XP_011523396.1:n.54-94_54-89del
XM_017024914.1:c.54-94_54-89del	XP_016880403.1:n.54-94_54-89del
XM_017024915.1:c.54-94_54-89del	XP_016880404.1:n.54-94_54-89del
XM_017024916.1:c.54-94_54-89del	XP_016880405.1:n.54-94_54-89del
XM_017024917.1:c.54-94_54-89del	XP_016880406.1:n.54-94_54-89del
XM_017024918.2:c.54-94_54-89del	XP_016880407.1:n.54-94_54-89del
XM_017024919.1:c.54-94_54-89del	XP_016880408.1:n.54-94_54-89del
XR_934513.3:n.909-94_909-89del
XR_934514.3:n.909-94_909-89del
NM_058216.3:c.405-94_405-89del MANE Select	NP_478123.1:n.405-94_405-89del
NR_103872.2:n.446+1410_446+1415del