Canonical Allele Identifier: CA3261181154
Community Standard Title: NM_058216.3(RAD51C):c.506_507delinsCC (p.Val169Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696794_58696795delinsCC , CM000679.2:g.58696794_58696795delinsCC GRCh38
NC_000017.10:g.56774155_56774156delinsCC , CM000679.1:g.56774155_56774156delinsCC GRCh37
NC_000017.9:g.54129154_54129155delinsCC NCBI36
NG_023199.1:g.9193_9194delinsCC , LRG_314:g.9193_9194delinsCC
NG_047169.1:g.285_286delinsGG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.506_507delinsCC MANE Select NP_478123.1:p.Val169Ala
ENST00000337432.9:c.506_507delinsCC MANE Select ENSP00000336701.4:p.Val169Ala
NM_058216.2:c.506_507delinsCC NP_478123.1:p.Val169Ala
NR_103872.1:n.475+1605_475+1606delinsCC
NR_103872.2:n.446+1605_446+1606delinsCC
ENST00000337432.8:c.506_507delinsCC ENSP00000336701.4:p.Val169Ala
ENST00000413590.5:c.144_145delinsCC
ENST00000425173.5:c.302_303delinsCC ENSP00000407282.1:p.Val101Ala
ENST00000461271.5:c.155_156delinsCC ENSP00000464056.1:p.Val52Ala
ENST00000461271.6:c.155_156delinsCC ENSP00000464056.2:p.Val52Ala
ENST00000475762.5:c.*1209_*1210delinsCC ENSP00000432421.1:n.*1209_*1210delinsCC
ENST00000482007.5:c.404+1605_404+1606delinsCC ENSP00000433332.1:n.404+1605_404+1606delinsCC
ENST00000487525.5:c.404+1605_404+1606delinsCC ENSP00000431637.1:n.404+1605_404+1606delinsCC
ENST00000487921.5:n.418_419delinsCC
ENST00000583539.5:c.506_507delinsCC ENSP00000463121.1:p.Val169Ala
ENST00000584617.5:c.228_229delinsCC
ENST00000622327.4:c.242_243delinsCC ENSP00000482326.1:p.Val81Ala
ENST00000697675.1:n.3103_3104delinsCC
ENST00000697676.1:n.566_567delinsCC
ENST00000697677.1:n.1587_1588delinsCC
ENST00000697678.1:n.408_409delinsCC
ENST00000697679.1:n.1580_1581delinsCC
ENST00000697680.1:c.*1370_*1371delinsCC ENSP00000513392.1:n.*1370_*1371delinsCC
ENST00000697681.1:c.*1397_*1398delinsCC ENSP00000513393.1:n.*1397_*1398delinsCC
ENST00000697683.1:c.*1370_*1371delinsCC ENSP00000513395.1:n.*1370_*1371delinsCC
ENST00000697684.1:n.566_567delinsCC
ENST00000697685.1:c.*1268+1605_*1268+1606delinsCC ENSP00000513396.1:n.*1268+1605_*1268+1606delinsCC
ENST00000697686.1:c.155_156delinsCC ENSP00000513397.1:p.Val52Ala
ENST00000697687.1:n.450+1605_450+1606delinsCC
ENST00000697688.1:n.552_553delinsCC
ENST00000697689.1:c.*1107+1605_*1107+1606delinsCC ENSP00000513398.1:n.*1107+1605_*1107+1606delinsCC
ENST00000697690.1:c.506_507delinsCC ENSP00000513399.1:p.Val169Ala
ENST00000697691.1:c.*478_*479delinsCC ENSP00000513400.1:n.*478_*479delinsCC
ENST00000697692.1:c.*518_*519delinsCC ENSP00000513401.1:n.*518_*519delinsCC
ENST00000697694.1:c.155_156delinsCC ENSP00000513402.1:p.Val52Ala
ENST00000697695.1:n.1113_1114delinsCC
XM_006722001.2:c.506_507delinsCC XP_006722064.1:p.Val169Ala
XM_006722001.4:c.506_507delinsCC XP_006722064.1:p.Val169Ala
XM_006722002.2:c.506_507delinsCC XP_006722065.1:p.Val169Ala
XM_006722002.4:c.506_507delinsCC XP_006722065.1:p.Val169Ala
XM_006722004.2:c.155_156delinsCC XP_006722067.1:p.Val52Ala
XM_006722004.3:c.155_156delinsCC XP_006722067.1:p.Val52Ala
XM_006722005.2:c.155_156delinsCC XP_006722068.1:p.Val52Ala
XM_006722005.3:c.155_156delinsCC XP_006722068.1:p.Val52Ala
XM_011525092.1:c.155_156delinsCC XP_011523394.1:p.Val52Ala
XM_011525092.2:c.155_156delinsCC XP_011523394.1:p.Val52Ala
XM_011525093.1:c.155_156delinsCC XP_011523395.1:p.Val52Ala
XM_011525093.2:c.155_156delinsCC XP_011523395.1:p.Val52Ala
XM_011525094.1:c.155_156delinsCC XP_011523396.1:p.Val52Ala
XM_011525094.2:c.155_156delinsCC XP_011523396.1:p.Val52Ala
XM_017024914.1:c.155_156delinsCC XP_016880403.1:p.Val52Ala
XM_017024915.1:c.155_156delinsCC XP_016880404.1:p.Val52Ala
XM_017024916.1:c.155_156delinsCC XP_016880405.1:p.Val52Ala
XM_017024917.1:c.155_156delinsCC XP_016880406.1:p.Val52Ala
XM_017024918.2:c.155_156delinsCC XP_016880407.1:p.Val52Ala
XM_017024919.1:c.155_156delinsCC XP_016880408.1:p.Val52Ala
XR_934513.1:n.579_580delinsCC
XR_934513.3:n.1010_1011delinsCC
XR_934514.1:n.579_580delinsCC
XR_934514.3:n.1010_1011delinsCC