Canonical Allele Identifier: CA3057229568

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696790_58696791delinsTA , CM000679.2:g.58696790_58696791delinsTA	GRCh38
NC_000017.10:g.56774151_56774152delinsTA , CM000679.1:g.56774151_56774152delinsTA	GRCh37
NC_000017.9:g.54129150_54129151delinsTA	NCBI36
NG_023199.1:g.9189_9190delinsTA , LRG_314:g.9189_9190delinsTA
NG_047169.1:g.289_290delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.151_152delinsTA	ENSP00000464056.2:p.Arg51Ter
ENST00000697675.1:n.3099_3100delinsTA
ENST00000697676.1:n.562_563delinsTA
ENST00000697677.1:n.1583_1584delinsTA
ENST00000697678.1:n.404_405delinsTA
ENST00000697679.1:n.1576_1577delinsTA
ENST00000697680.1:c.*1366_*1367delinsTA	ENSP00000513392.1:n.*1366_*1367delinsTA
ENST00000697681.1:c.*1393_*1394delinsTA	ENSP00000513393.1:n.*1393_*1394delinsTA
ENST00000697683.1:c.*1366_*1367delinsTA	ENSP00000513395.1:n.*1366_*1367delinsTA
ENST00000697684.1:n.562_563delinsTA
ENST00000697685.1:c.*1268+1601_*1268+1602delinsTA	ENSP00000513396.1:n.*1268+1601_*1268+1602delinsTA
ENST00000697686.1:c.151_152delinsTA	ENSP00000513397.1:p.Arg51Ter
ENST00000697687.1:n.450+1601_450+1602delinsTA
ENST00000697688.1:n.548_549delinsTA
ENST00000697689.1:c.*1107+1601_*1107+1602delinsTA	ENSP00000513398.1:n.*1107+1601_*1107+1602delinsTA
ENST00000697690.1:c.502_503delinsTA	ENSP00000513399.1:p.Arg168Ter
ENST00000697691.1:c.*474_*475delinsTA	ENSP00000513400.1:n.*474_*475delinsTA
ENST00000697692.1:c.*514_*515delinsTA	ENSP00000513401.1:n.*514_*515delinsTA
ENST00000697694.1:c.151_152delinsTA	ENSP00000513402.1:p.Arg51Ter
ENST00000697695.1:n.1109_1110delinsTA
ENST00000337432.9:c.502_503delinsTA MANE Select	ENSP00000336701.4:p.Arg168Ter
ENST00000337432.8:c.502_503delinsTA	ENSP00000336701.4:p.Arg168Ter
ENST00000413590.5:c.140_141delinsTA
ENST00000425173.5:c.298_299delinsTA	ENSP00000407282.1:p.Arg100Ter
ENST00000461271.5:c.151_152delinsTA	ENSP00000464056.1:p.Arg51Ter
ENST00000475762.5:c.*1205_*1206delinsTA	ENSP00000432421.1:n.*1205_*1206delinsTA
ENST00000482007.5:c.404+1601_404+1602delinsTA	ENSP00000433332.1:n.404+1601_404+1602delinsTA
ENST00000487525.5:c.404+1601_404+1602delinsTA	ENSP00000431637.1:n.404+1601_404+1602delinsTA
ENST00000487921.5:n.414_415delinsTA
ENST00000583539.5:c.502_503delinsTA	ENSP00000463121.1:p.Arg168Ter
ENST00000584617.5:c.224_225delinsTA
ENST00000622327.4:c.238_239delinsTA	ENSP00000482326.1:p.Arg80Ter
NM_058216.2:c.502_503delinsTA	NP_478123.1:p.Arg168Ter
NR_103872.1:n.475+1601_475+1602delinsTA
XM_006722001.2:c.502_503delinsTA	XP_006722064.1:p.Arg168Ter
XM_006722002.2:c.502_503delinsTA	XP_006722065.1:p.Arg168Ter
XM_006722004.2:c.151_152delinsTA	XP_006722067.1:p.Arg51Ter
XM_006722005.2:c.151_152delinsTA	XP_006722068.1:p.Arg51Ter
XM_011525092.1:c.151_152delinsTA	XP_011523394.1:p.Arg51Ter
XM_011525093.1:c.151_152delinsTA	XP_011523395.1:p.Arg51Ter
XM_011525094.1:c.151_152delinsTA	XP_011523396.1:p.Arg51Ter
XR_934513.1:n.575_576delinsTA
XR_934514.1:n.575_576delinsTA
XM_006722001.4:c.502_503delinsTA	XP_006722064.1:p.Arg168Ter
XM_006722002.4:c.502_503delinsTA	XP_006722065.1:p.Arg168Ter
XM_006722004.3:c.151_152delinsTA	XP_006722067.1:p.Arg51Ter
XM_006722005.3:c.151_152delinsTA	XP_006722068.1:p.Arg51Ter
XM_011525092.2:c.151_152delinsTA	XP_011523394.1:p.Arg51Ter
XM_011525093.2:c.151_152delinsTA	XP_011523395.1:p.Arg51Ter
XM_011525094.2:c.151_152delinsTA	XP_011523396.1:p.Arg51Ter
XM_017024914.1:c.151_152delinsTA	XP_016880403.1:p.Arg51Ter
XM_017024915.1:c.151_152delinsTA	XP_016880404.1:p.Arg51Ter
XM_017024916.1:c.151_152delinsTA	XP_016880405.1:p.Arg51Ter
XM_017024917.1:c.151_152delinsTA	XP_016880406.1:p.Arg51Ter
XM_017024918.2:c.151_152delinsTA	XP_016880407.1:p.Arg51Ter
XM_017024919.1:c.151_152delinsTA	XP_016880408.1:p.Arg51Ter
XR_934513.3:n.1006_1007delinsTA
XR_934514.3:n.1006_1007delinsTA
NM_058216.3:c.502_503delinsTA MANE Select	NP_478123.1:p.Arg168Ter
NR_103872.2:n.446+1601_446+1602delinsTA