Canonical Allele Identifier: CA3261181124
Community Standard Title: NM_058216.3(RAD51C):c.500_501delinsCC (p.Asp167Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696788_58696789delinsCC , CM000679.2:g.58696788_58696789delinsCC GRCh38
NC_000017.10:g.56774149_56774150delinsCC , CM000679.1:g.56774149_56774150delinsCC GRCh37
NC_000017.9:g.54129148_54129149delinsCC NCBI36
NG_023199.1:g.9187_9188delinsCC , LRG_314:g.9187_9188delinsCC
NG_047169.1:g.291_292delinsGG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.500_501delinsCC MANE Select NP_478123.1:p.Asp167Ala
ENST00000337432.9:c.500_501delinsCC MANE Select ENSP00000336701.4:p.Asp167Ala
NM_058216.2:c.500_501delinsCC NP_478123.1:p.Asp167Ala
NR_103872.1:n.475+1599_475+1600delinsCC
NR_103872.2:n.446+1599_446+1600delinsCC
ENST00000337432.8:c.500_501delinsCC ENSP00000336701.4:p.Asp167Ala
ENST00000413590.5:c.138_139delinsCC
ENST00000425173.5:c.296_297delinsCC ENSP00000407282.1:p.Asp99Ala
ENST00000461271.5:c.149_150delinsCC ENSP00000464056.1:p.Asp50Ala
ENST00000461271.6:c.149_150delinsCC ENSP00000464056.2:p.Asp50Ala
ENST00000475762.5:c.*1203_*1204delinsCC ENSP00000432421.1:n.*1203_*1204delinsCC
ENST00000482007.5:c.404+1599_404+1600delinsCC ENSP00000433332.1:n.404+1599_404+1600delinsCC
ENST00000487525.5:c.404+1599_404+1600delinsCC ENSP00000431637.1:n.404+1599_404+1600delinsCC
ENST00000487921.5:n.412_413delinsCC
ENST00000583539.5:c.500_501delinsCC ENSP00000463121.1:p.Asp167Ala
ENST00000584617.5:c.222_223delinsCC
ENST00000622327.4:c.236_237delinsCC ENSP00000482326.1:p.Asp79Ala
ENST00000697675.1:n.3097_3098delinsCC
ENST00000697676.1:n.560_561delinsCC
ENST00000697677.1:n.1581_1582delinsCC
ENST00000697678.1:n.402_403delinsCC
ENST00000697679.1:n.1574_1575delinsCC
ENST00000697680.1:c.*1364_*1365delinsCC ENSP00000513392.1:n.*1364_*1365delinsCC
ENST00000697681.1:c.*1391_*1392delinsCC ENSP00000513393.1:n.*1391_*1392delinsCC
ENST00000697683.1:c.*1364_*1365delinsCC ENSP00000513395.1:n.*1364_*1365delinsCC
ENST00000697684.1:n.560_561delinsCC
ENST00000697685.1:c.*1268+1599_*1268+1600delinsCC ENSP00000513396.1:n.*1268+1599_*1268+1600delinsCC
ENST00000697686.1:c.149_150delinsCC ENSP00000513397.1:p.Asp50Ala
ENST00000697687.1:n.450+1599_450+1600delinsCC
ENST00000697688.1:n.546_547delinsCC
ENST00000697689.1:c.*1107+1599_*1107+1600delinsCC ENSP00000513398.1:n.*1107+1599_*1107+1600delinsCC
ENST00000697690.1:c.500_501delinsCC ENSP00000513399.1:p.Asp167Ala
ENST00000697691.1:c.*472_*473delinsCC ENSP00000513400.1:n.*472_*473delinsCC
ENST00000697692.1:c.*512_*513delinsCC ENSP00000513401.1:n.*512_*513delinsCC
ENST00000697694.1:c.149_150delinsCC ENSP00000513402.1:p.Asp50Ala
ENST00000697695.1:n.1107_1108delinsCC
XM_006722001.2:c.500_501delinsCC XP_006722064.1:p.Asp167Ala
XM_006722001.4:c.500_501delinsCC XP_006722064.1:p.Asp167Ala
XM_006722002.2:c.500_501delinsCC XP_006722065.1:p.Asp167Ala
XM_006722002.4:c.500_501delinsCC XP_006722065.1:p.Asp167Ala
XM_006722004.2:c.149_150delinsCC XP_006722067.1:p.Asp50Ala
XM_006722004.3:c.149_150delinsCC XP_006722067.1:p.Asp50Ala
XM_006722005.2:c.149_150delinsCC XP_006722068.1:p.Asp50Ala
XM_006722005.3:c.149_150delinsCC XP_006722068.1:p.Asp50Ala
XM_011525092.1:c.149_150delinsCC XP_011523394.1:p.Asp50Ala
XM_011525092.2:c.149_150delinsCC XP_011523394.1:p.Asp50Ala
XM_011525093.1:c.149_150delinsCC XP_011523395.1:p.Asp50Ala
XM_011525093.2:c.149_150delinsCC XP_011523395.1:p.Asp50Ala
XM_011525094.1:c.149_150delinsCC XP_011523396.1:p.Asp50Ala
XM_011525094.2:c.149_150delinsCC XP_011523396.1:p.Asp50Ala
XM_017024914.1:c.149_150delinsCC XP_016880403.1:p.Asp50Ala
XM_017024915.1:c.149_150delinsCC XP_016880404.1:p.Asp50Ala
XM_017024916.1:c.149_150delinsCC XP_016880405.1:p.Asp50Ala
XM_017024917.1:c.149_150delinsCC XP_016880406.1:p.Asp50Ala
XM_017024918.2:c.149_150delinsCC XP_016880407.1:p.Asp50Ala
XM_017024919.1:c.149_150delinsCC XP_016880408.1:p.Asp50Ala
XR_934513.1:n.573_574delinsCC
XR_934513.3:n.1004_1005delinsCC
XR_934514.1:n.573_574delinsCC
XR_934514.3:n.1004_1005delinsCC