Canonical Allele Identifier: CA3261180884
Community Standard Title: NM_058216.3(RAD51C):c.461_462delinsGC (p.Glu154Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696749_58696750delinsGC , CM000679.2:g.58696749_58696750delinsGC GRCh38
NC_000017.10:g.56774110_56774111delinsGC , CM000679.1:g.56774110_56774111delinsGC GRCh37
NC_000017.9:g.54129109_54129110delinsGC NCBI36
NG_023199.1:g.9148_9149delinsGC , LRG_314:g.9148_9149delinsGC
NG_047169.1:g.330_331delinsGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.461_462delinsGC MANE Select NP_478123.1:p.Glu154Gly
ENST00000337432.9:c.461_462delinsGC MANE Select ENSP00000336701.4:p.Glu154Gly
NM_058216.2:c.461_462delinsGC NP_478123.1:p.Glu154Gly
NR_103872.1:n.475+1560_475+1561delinsGC
NR_103872.2:n.446+1560_446+1561delinsGC
ENST00000337432.8:c.461_462delinsGC ENSP00000336701.4:p.Glu154Gly
ENST00000413590.5:c.99_100delinsGC
ENST00000425173.5:c.257_258delinsGC ENSP00000407282.1:p.Glu86Gly
ENST00000461271.5:c.110_111delinsGC ENSP00000464056.1:p.Glu37Gly
ENST00000461271.6:c.110_111delinsGC ENSP00000464056.2:p.Glu37Gly
ENST00000475762.5:c.*1164_*1165delinsGC ENSP00000432421.1:n.*1164_*1165delinsGC
ENST00000482007.5:c.404+1560_404+1561delinsGC ENSP00000433332.1:n.404+1560_404+1561delinsGC
ENST00000487525.5:c.404+1560_404+1561delinsGC ENSP00000431637.1:n.404+1560_404+1561delinsGC
ENST00000487921.5:n.373_374delinsGC
ENST00000583539.5:c.461_462delinsGC ENSP00000463121.1:p.Glu154Gly
ENST00000584617.5:c.183_184delinsGC
ENST00000622327.4:c.197_198delinsGC ENSP00000482326.1:p.Glu66Gly
ENST00000697675.1:n.3058_3059delinsGC
ENST00000697676.1:n.521_522delinsGC
ENST00000697677.1:n.1542_1543delinsGC
ENST00000697678.1:n.363_364delinsGC
ENST00000697679.1:n.1535_1536delinsGC
ENST00000697680.1:c.*1325_*1326delinsGC ENSP00000513392.1:n.*1325_*1326delinsGC
ENST00000697681.1:c.*1352_*1353delinsGC ENSP00000513393.1:n.*1352_*1353delinsGC
ENST00000697683.1:c.*1325_*1326delinsGC ENSP00000513395.1:n.*1325_*1326delinsGC
ENST00000697684.1:n.521_522delinsGC
ENST00000697685.1:c.*1268+1560_*1268+1561delinsGC ENSP00000513396.1:n.*1268+1560_*1268+1561delinsGC
ENST00000697686.1:c.110_111delinsGC ENSP00000513397.1:p.Glu37Gly
ENST00000697687.1:n.450+1560_450+1561delinsGC
ENST00000697688.1:n.507_508delinsGC
ENST00000697689.1:c.*1107+1560_*1107+1561delinsGC ENSP00000513398.1:n.*1107+1560_*1107+1561delinsGC
ENST00000697690.1:c.461_462delinsGC ENSP00000513399.1:p.Glu154Gly
ENST00000697691.1:c.*433_*434delinsGC ENSP00000513400.1:n.*433_*434delinsGC
ENST00000697692.1:c.*473_*474delinsGC ENSP00000513401.1:n.*473_*474delinsGC
ENST00000697694.1:c.110_111delinsGC ENSP00000513402.1:p.Glu37Gly
ENST00000697695.1:n.1068_1069delinsGC
XM_006722001.2:c.461_462delinsGC XP_006722064.1:p.Glu154Gly
XM_006722001.4:c.461_462delinsGC XP_006722064.1:p.Glu154Gly
XM_006722002.2:c.461_462delinsGC XP_006722065.1:p.Glu154Gly
XM_006722002.4:c.461_462delinsGC XP_006722065.1:p.Glu154Gly
XM_006722004.2:c.110_111delinsGC XP_006722067.1:p.Glu37Gly
XM_006722004.3:c.110_111delinsGC XP_006722067.1:p.Glu37Gly
XM_006722005.2:c.110_111delinsGC XP_006722068.1:p.Glu37Gly
XM_006722005.3:c.110_111delinsGC XP_006722068.1:p.Glu37Gly
XM_011525092.1:c.110_111delinsGC XP_011523394.1:p.Glu37Gly
XM_011525092.2:c.110_111delinsGC XP_011523394.1:p.Glu37Gly
XM_011525093.1:c.110_111delinsGC XP_011523395.1:p.Glu37Gly
XM_011525093.2:c.110_111delinsGC XP_011523395.1:p.Glu37Gly
XM_011525094.1:c.110_111delinsGC XP_011523396.1:p.Glu37Gly
XM_011525094.2:c.110_111delinsGC XP_011523396.1:p.Glu37Gly
XM_017024914.1:c.110_111delinsGC XP_016880403.1:p.Glu37Gly
XM_017024915.1:c.110_111delinsGC XP_016880404.1:p.Glu37Gly
XM_017024916.1:c.110_111delinsGC XP_016880405.1:p.Glu37Gly
XM_017024917.1:c.110_111delinsGC XP_016880406.1:p.Glu37Gly
XM_017024918.2:c.110_111delinsGC XP_016880407.1:p.Glu37Gly
XM_017024919.1:c.110_111delinsGC XP_016880408.1:p.Glu37Gly
XR_934513.1:n.534_535delinsGC
XR_934513.3:n.965_966delinsGC
XR_934514.1:n.534_535delinsGC
XR_934514.3:n.965_966delinsGC