Canonical Allele Identifier: CA3261180811
Community Standard Title: NM_058216.3(RAD51C):c.451_453delinsCTC (p.Val151Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696739_58696741delinsCTC , CM000679.2:g.58696739_58696741delinsCTC GRCh38
NC_000017.10:g.56774100_56774102delinsCTC , CM000679.1:g.56774100_56774102delinsCTC GRCh37
NC_000017.9:g.54129099_54129101delinsCTC NCBI36
NG_023199.1:g.9138_9140delinsCTC , LRG_314:g.9138_9140delinsCTC
NG_047169.1:g.339_341delinsGAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.451_453delinsCTC MANE Select NP_478123.1:p.Val151Leu
ENST00000337432.9:c.451_453delinsCTC MANE Select ENSP00000336701.4:p.Val151Leu
NM_058216.2:c.451_453delinsCTC NP_478123.1:p.Val151Leu
NR_103872.1:n.475+1550_475+1552delinsCTC
NR_103872.2:n.446+1550_446+1552delinsCTC
ENST00000337432.8:c.451_453delinsCTC ENSP00000336701.4:p.Val151Leu
ENST00000413590.5:c.89_91delinsCTC
ENST00000425173.5:c.247_249delinsCTC ENSP00000407282.1:p.Val83Leu
ENST00000461271.5:c.100_102delinsCTC ENSP00000464056.1:p.Val34Leu
ENST00000461271.6:c.100_102delinsCTC ENSP00000464056.2:p.Val34Leu
ENST00000475762.5:c.*1154_*1156delinsCTC ENSP00000432421.1:n.*1154_*1156delinsCTC
ENST00000482007.5:c.404+1550_404+1552delinsCTC ENSP00000433332.1:n.404+1550_404+1552delinsCTC
ENST00000487525.5:c.404+1550_404+1552delinsCTC ENSP00000431637.1:n.404+1550_404+1552delinsCTC
ENST00000487921.5:n.363_365delinsCTC
ENST00000583539.5:c.451_453delinsCTC ENSP00000463121.1:p.Val151Leu
ENST00000584617.5:c.173_175delinsCTC
ENST00000622327.4:c.187_189delinsCTC ENSP00000482326.1:p.Val63Leu
ENST00000697675.1:n.3048_3050delinsCTC
ENST00000697676.1:n.511_513delinsCTC
ENST00000697677.1:n.1532_1534delinsCTC
ENST00000697678.1:n.353_355delinsCTC
ENST00000697679.1:n.1525_1527delinsCTC
ENST00000697680.1:c.*1315_*1317delinsCTC ENSP00000513392.1:n.*1315_*1317delinsCTC
ENST00000697681.1:c.*1342_*1344delinsCTC ENSP00000513393.1:n.*1342_*1344delinsCTC
ENST00000697683.1:c.*1315_*1317delinsCTC ENSP00000513395.1:n.*1315_*1317delinsCTC
ENST00000697684.1:n.511_513delinsCTC
ENST00000697685.1:c.*1268+1550_*1268+1552delinsCTC ENSP00000513396.1:n.*1268+1550_*1268+1552delinsCTC
ENST00000697686.1:c.100_102delinsCTC ENSP00000513397.1:p.Val34Leu
ENST00000697687.1:n.450+1550_450+1552delinsCTC
ENST00000697688.1:n.497_499delinsCTC
ENST00000697689.1:c.*1107+1550_*1107+1552delinsCTC ENSP00000513398.1:n.*1107+1550_*1107+1552delinsCTC
ENST00000697690.1:c.451_453delinsCTC ENSP00000513399.1:p.Val151Leu
ENST00000697691.1:c.*423_*425delinsCTC ENSP00000513400.1:n.*423_*425delinsCTC
ENST00000697692.1:c.*463_*465delinsCTC ENSP00000513401.1:n.*463_*465delinsCTC
ENST00000697694.1:c.100_102delinsCTC ENSP00000513402.1:p.Val34Leu
ENST00000697695.1:n.1058_1060delinsCTC
XM_006722001.2:c.451_453delinsCTC XP_006722064.1:p.Val151Leu
XM_006722001.4:c.451_453delinsCTC XP_006722064.1:p.Val151Leu
XM_006722002.2:c.451_453delinsCTC XP_006722065.1:p.Val151Leu
XM_006722002.4:c.451_453delinsCTC XP_006722065.1:p.Val151Leu
XM_006722004.2:c.100_102delinsCTC XP_006722067.1:p.Val34Leu
XM_006722004.3:c.100_102delinsCTC XP_006722067.1:p.Val34Leu
XM_006722005.2:c.100_102delinsCTC XP_006722068.1:p.Val34Leu
XM_006722005.3:c.100_102delinsCTC XP_006722068.1:p.Val34Leu
XM_011525092.1:c.100_102delinsCTC XP_011523394.1:p.Val34Leu
XM_011525092.2:c.100_102delinsCTC XP_011523394.1:p.Val34Leu
XM_011525093.1:c.100_102delinsCTC XP_011523395.1:p.Val34Leu
XM_011525093.2:c.100_102delinsCTC XP_011523395.1:p.Val34Leu
XM_011525094.1:c.100_102delinsCTC XP_011523396.1:p.Val34Leu
XM_011525094.2:c.100_102delinsCTC XP_011523396.1:p.Val34Leu
XM_017024914.1:c.100_102delinsCTC XP_016880403.1:p.Val34Leu
XM_017024915.1:c.100_102delinsCTC XP_016880404.1:p.Val34Leu
XM_017024916.1:c.100_102delinsCTC XP_016880405.1:p.Val34Leu
XM_017024917.1:c.100_102delinsCTC XP_016880406.1:p.Val34Leu
XM_017024918.2:c.100_102delinsCTC XP_016880407.1:p.Val34Leu
XM_017024919.1:c.100_102delinsCTC XP_016880408.1:p.Val34Leu
XR_934513.1:n.524_526delinsCTC
XR_934513.3:n.955_957delinsCTC
XR_934514.1:n.524_526delinsCTC
XR_934514.3:n.955_957delinsCTC