Canonical Allele Identifier: CA3261180828
Community Standard Title: NM_058216.3(RAD51C):c.454_456delinsAGC (p.Ala152Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696742_58696744delinsAGC , CM000679.2:g.58696742_58696744delinsAGC GRCh38
NC_000017.10:g.56774103_56774105delinsAGC , CM000679.1:g.56774103_56774105delinsAGC GRCh37
NC_000017.9:g.54129102_54129104delinsAGC NCBI36
NG_023199.1:g.9141_9143delinsAGC , LRG_314:g.9141_9143delinsAGC
NG_047169.1:g.336_338delinsGCT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.454_456delinsAGC MANE Select NP_478123.1:p.Ala152Ser
ENST00000337432.9:c.454_456delinsAGC MANE Select ENSP00000336701.4:p.Ala152Ser
NM_058216.2:c.454_456delinsAGC NP_478123.1:p.Ala152Ser
NR_103872.1:n.475+1553_475+1555delinsAGC
NR_103872.2:n.446+1553_446+1555delinsAGC
ENST00000337432.8:c.454_456delinsAGC ENSP00000336701.4:p.Ala152Ser
ENST00000413590.5:c.92_94delinsAGC
ENST00000425173.5:c.250_252delinsAGC ENSP00000407282.1:p.Ala84Ser
ENST00000461271.5:c.103_105delinsAGC ENSP00000464056.1:p.Ala35Ser
ENST00000461271.6:c.103_105delinsAGC ENSP00000464056.2:p.Ala35Ser
ENST00000475762.5:c.*1157_*1159delinsAGC ENSP00000432421.1:n.*1157_*1159delinsAGC
ENST00000482007.5:c.404+1553_404+1555delinsAGC ENSP00000433332.1:n.404+1553_404+1555delinsAGC
ENST00000487525.5:c.404+1553_404+1555delinsAGC ENSP00000431637.1:n.404+1553_404+1555delinsAGC
ENST00000487921.5:n.366_368delinsAGC
ENST00000583539.5:c.454_456delinsAGC ENSP00000463121.1:p.Ala152Ser
ENST00000584617.5:c.176_178delinsAGC
ENST00000622327.4:c.190_192delinsAGC ENSP00000482326.1:p.Ala64Ser
ENST00000697675.1:n.3051_3053delinsAGC
ENST00000697676.1:n.514_516delinsAGC
ENST00000697677.1:n.1535_1537delinsAGC
ENST00000697678.1:n.356_358delinsAGC
ENST00000697679.1:n.1528_1530delinsAGC
ENST00000697680.1:c.*1318_*1320delinsAGC ENSP00000513392.1:n.*1318_*1320delinsAGC
ENST00000697681.1:c.*1345_*1347delinsAGC ENSP00000513393.1:n.*1345_*1347delinsAGC
ENST00000697683.1:c.*1318_*1320delinsAGC ENSP00000513395.1:n.*1318_*1320delinsAGC
ENST00000697684.1:n.514_516delinsAGC
ENST00000697685.1:c.*1268+1553_*1268+1555delinsAGC ENSP00000513396.1:n.*1268+1553_*1268+1555delinsAGC
ENST00000697686.1:c.103_105delinsAGC ENSP00000513397.1:p.Ala35Ser
ENST00000697687.1:n.450+1553_450+1555delinsAGC
ENST00000697688.1:n.500_502delinsAGC
ENST00000697689.1:c.*1107+1553_*1107+1555delinsAGC ENSP00000513398.1:n.*1107+1553_*1107+1555delinsAGC
ENST00000697690.1:c.454_456delinsAGC ENSP00000513399.1:p.Ala152Ser
ENST00000697691.1:c.*426_*428delinsAGC ENSP00000513400.1:n.*426_*428delinsAGC
ENST00000697692.1:c.*466_*468delinsAGC ENSP00000513401.1:n.*466_*468delinsAGC
ENST00000697694.1:c.103_105delinsAGC ENSP00000513402.1:p.Ala35Ser
ENST00000697695.1:n.1061_1063delinsAGC
XM_006722001.2:c.454_456delinsAGC XP_006722064.1:p.Ala152Ser
XM_006722001.4:c.454_456delinsAGC XP_006722064.1:p.Ala152Ser
XM_006722002.2:c.454_456delinsAGC XP_006722065.1:p.Ala152Ser
XM_006722002.4:c.454_456delinsAGC XP_006722065.1:p.Ala152Ser
XM_006722004.2:c.103_105delinsAGC XP_006722067.1:p.Ala35Ser
XM_006722004.3:c.103_105delinsAGC XP_006722067.1:p.Ala35Ser
XM_006722005.2:c.103_105delinsAGC XP_006722068.1:p.Ala35Ser
XM_006722005.3:c.103_105delinsAGC XP_006722068.1:p.Ala35Ser
XM_011525092.1:c.103_105delinsAGC XP_011523394.1:p.Ala35Ser
XM_011525092.2:c.103_105delinsAGC XP_011523394.1:p.Ala35Ser
XM_011525093.1:c.103_105delinsAGC XP_011523395.1:p.Ala35Ser
XM_011525093.2:c.103_105delinsAGC XP_011523395.1:p.Ala35Ser
XM_011525094.1:c.103_105delinsAGC XP_011523396.1:p.Ala35Ser
XM_011525094.2:c.103_105delinsAGC XP_011523396.1:p.Ala35Ser
XM_017024914.1:c.103_105delinsAGC XP_016880403.1:p.Ala35Ser
XM_017024915.1:c.103_105delinsAGC XP_016880404.1:p.Ala35Ser
XM_017024916.1:c.103_105delinsAGC XP_016880405.1:p.Ala35Ser
XM_017024917.1:c.103_105delinsAGC XP_016880406.1:p.Ala35Ser
XM_017024918.2:c.103_105delinsAGC XP_016880407.1:p.Ala35Ser
XM_017024919.1:c.103_105delinsAGC XP_016880408.1:p.Ala35Ser
XR_934513.1:n.527_529delinsAGC
XR_934513.3:n.958_960delinsAGC
XR_934514.1:n.527_529delinsAGC
XR_934514.3:n.958_960delinsAGC