Canonical Allele Identifier: CA3261180747
Community Standard Title: NM_058216.3(RAD51C):c.440_441delinsAC (p.Cys147Tyr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696728_58696729delinsAC , CM000679.2:g.58696728_58696729delinsAC GRCh38
NC_000017.10:g.56774089_56774090delinsAC , CM000679.1:g.56774089_56774090delinsAC GRCh37
NC_000017.9:g.54129088_54129089delinsAC NCBI36
NG_023199.1:g.9127_9128delinsAC , LRG_314:g.9127_9128delinsAC
NG_047169.1:g.351_352delinsGT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.440_441delinsAC MANE Select NP_478123.1:p.Cys147Tyr
ENST00000337432.9:c.440_441delinsAC MANE Select ENSP00000336701.4:p.Cys147Tyr
NM_058216.2:c.440_441delinsAC NP_478123.1:p.Cys147Tyr
NR_103872.1:n.475+1539_475+1540delinsAC
NR_103872.2:n.446+1539_446+1540delinsAC
ENST00000337432.8:c.440_441delinsAC ENSP00000336701.4:p.Cys147Tyr
ENST00000413590.5:c.78_79delinsAC
ENST00000425173.5:c.236_237delinsAC ENSP00000407282.1:p.Cys79Tyr
ENST00000461271.5:c.89_90delinsAC ENSP00000464056.1:p.Cys30Tyr
ENST00000461271.6:c.89_90delinsAC ENSP00000464056.2:p.Cys30Tyr
ENST00000475762.5:c.*1143_*1144delinsAC ENSP00000432421.1:n.*1143_*1144delinsAC
ENST00000482007.5:c.404+1539_404+1540delinsAC ENSP00000433332.1:n.404+1539_404+1540delinsAC
ENST00000487525.5:c.404+1539_404+1540delinsAC ENSP00000431637.1:n.404+1539_404+1540delinsAC
ENST00000487921.5:n.352_353delinsAC
ENST00000583539.5:c.440_441delinsAC ENSP00000463121.1:p.Cys147Tyr
ENST00000584617.5:c.162_163delinsAC
ENST00000622327.4:c.176_177delinsAC ENSP00000482326.1:p.Cys59Tyr
ENST00000697675.1:n.3037_3038delinsAC
ENST00000697676.1:n.500_501delinsAC
ENST00000697677.1:n.1521_1522delinsAC
ENST00000697678.1:n.342_343delinsAC
ENST00000697679.1:n.1514_1515delinsAC
ENST00000697680.1:c.*1304_*1305delinsAC ENSP00000513392.1:n.*1304_*1305delinsAC
ENST00000697681.1:c.*1331_*1332delinsAC ENSP00000513393.1:n.*1331_*1332delinsAC
ENST00000697683.1:c.*1304_*1305delinsAC ENSP00000513395.1:n.*1304_*1305delinsAC
ENST00000697684.1:n.500_501delinsAC
ENST00000697685.1:c.*1268+1539_*1268+1540delinsAC ENSP00000513396.1:n.*1268+1539_*1268+1540delinsAC
ENST00000697686.1:c.89_90delinsAC ENSP00000513397.1:p.Cys30Tyr
ENST00000697687.1:n.450+1539_450+1540delinsAC
ENST00000697688.1:n.486_487delinsAC
ENST00000697689.1:c.*1107+1539_*1107+1540delinsAC ENSP00000513398.1:n.*1107+1539_*1107+1540delinsAC
ENST00000697690.1:c.440_441delinsAC ENSP00000513399.1:p.Cys147Tyr
ENST00000697691.1:c.*412_*413delinsAC ENSP00000513400.1:n.*412_*413delinsAC
ENST00000697692.1:c.*452_*453delinsAC ENSP00000513401.1:n.*452_*453delinsAC
ENST00000697694.1:c.89_90delinsAC ENSP00000513402.1:p.Cys30Tyr
ENST00000697695.1:n.1047_1048delinsAC
XM_006722001.2:c.440_441delinsAC XP_006722064.1:p.Cys147Tyr
XM_006722001.4:c.440_441delinsAC XP_006722064.1:p.Cys147Tyr
XM_006722002.2:c.440_441delinsAC XP_006722065.1:p.Cys147Tyr
XM_006722002.4:c.440_441delinsAC XP_006722065.1:p.Cys147Tyr
XM_006722004.2:c.89_90delinsAC XP_006722067.1:p.Cys30Tyr
XM_006722004.3:c.89_90delinsAC XP_006722067.1:p.Cys30Tyr
XM_006722005.2:c.89_90delinsAC XP_006722068.1:p.Cys30Tyr
XM_006722005.3:c.89_90delinsAC XP_006722068.1:p.Cys30Tyr
XM_011525092.1:c.89_90delinsAC XP_011523394.1:p.Cys30Tyr
XM_011525092.2:c.89_90delinsAC XP_011523394.1:p.Cys30Tyr
XM_011525093.1:c.89_90delinsAC XP_011523395.1:p.Cys30Tyr
XM_011525093.2:c.89_90delinsAC XP_011523395.1:p.Cys30Tyr
XM_011525094.1:c.89_90delinsAC XP_011523396.1:p.Cys30Tyr
XM_011525094.2:c.89_90delinsAC XP_011523396.1:p.Cys30Tyr
XM_017024914.1:c.89_90delinsAC XP_016880403.1:p.Cys30Tyr
XM_017024915.1:c.89_90delinsAC XP_016880404.1:p.Cys30Tyr
XM_017024916.1:c.89_90delinsAC XP_016880405.1:p.Cys30Tyr
XM_017024917.1:c.89_90delinsAC XP_016880406.1:p.Cys30Tyr
XM_017024918.2:c.89_90delinsAC XP_016880407.1:p.Cys30Tyr
XM_017024919.1:c.89_90delinsAC XP_016880408.1:p.Cys30Tyr
XR_934513.1:n.513_514delinsAC
XR_934513.3:n.944_945delinsAC
XR_934514.1:n.513_514delinsAC
XR_934514.3:n.944_945delinsAC