Canonical Allele Identifier: CA3057229279
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695174dup , CM000679.2:g.58695174dup GRCh38
NC_000017.10:g.56772535dup , CM000679.1:g.56772535dup GRCh37
NC_000017.9:g.54127534dup NCBI36
NG_023199.1:g.7573dup , LRG_314:g.7573dup
NG_047169.1:g.1907dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.38dup ENSP00000464056.2:p.Thr15AsnfsTer23
ENST00000697675.1:n.1483dup
ENST00000697676.1:n.449dup
ENST00000697677.1:n.1470dup
ENST00000697678.1:n.291dup
ENST00000697679.1:n.1463dup
ENST00000697680.1:c.*1253dup ENSP00000513392.1:n.*1253dup
ENST00000697681.1:c.*1253dup ENSP00000513393.1:n.*1253dup
ENST00000697683.1:c.*1253dup ENSP00000513395.1:n.*1253dup
ENST00000697684.1:n.449dup
ENST00000697685.1:c.*1253dup ENSP00000513396.1:n.*1253dup
ENST00000697686.1:c.38dup ENSP00000513397.1:p.Thr15AsnfsTer23
ENST00000697687.1:n.435dup
ENST00000697688.1:n.435dup
ENST00000697689.1:c.*1092dup ENSP00000513398.1:n.*1092dup
ENST00000697690.1:c.389dup ENSP00000513399.1:p.Thr132AsnfsTer23
ENST00000697691.1:c.*361dup ENSP00000513400.1:n.*361dup
ENST00000697692.1:c.*401dup ENSP00000513401.1:n.*401dup
ENST00000697693.1:n.1164dup
ENST00000697694.1:c.38dup ENSP00000513402.1:p.Thr15AsnfsTer23
ENST00000697695.1:n.996dup
ENST00000337432.9:c.389dup MANE Select ENSP00000336701.4:p.Thr132AsnfsTer23
ENST00000337432.8:c.389dup ENSP00000336701.4:p.Thr132AsnfsTer23
ENST00000413590.5:c.27dup
ENST00000421782.3:c.389dup ENSP00000391450.2:p.Thr132AsnfsTer7
ENST00000425173.5:c.185dup ENSP00000407282.1:p.Thr64AsnfsTer23
ENST00000461271.5:c.38dup ENSP00000464056.1:p.Thr15AsnfsTer23
ENST00000475762.5:c.*1092dup ENSP00000432421.1:n.*1092dup
ENST00000482007.5:c.389dup ENSP00000433332.1:p.Thr132AsnfsTer?
ENST00000486827.1:c.*1253dup ENSP00000436761.1:n.*1253dup
ENST00000487525.5:c.389dup ENSP00000431637.1:p.Thr132AsnfsTer?
ENST00000487921.5:n.301dup
ENST00000583539.5:c.389dup ENSP00000463121.1:p.Thr132AsnfsTer23
ENST00000584617.5:c.127-1519dup
ENST00000622327.4:c.125dup ENSP00000482326.1:p.Thr44AsnfsTer23
NM_002876.3:c.389dup NP_002867.1:p.Thr132AsnfsTer7
NM_058216.2:c.389dup NP_478123.1:p.Thr132AsnfsTer23
NR_103872.1:n.460dup
NR_103873.1:n.357dup
XM_006722001.2:c.389dup XP_006722064.1:p.Thr132AsnfsTer23
XM_006722002.2:c.389dup XP_006722065.1:p.Thr132AsnfsTer23
XM_006722004.2:c.38dup XP_006722067.1:p.Thr15AsnfsTer23
XM_006722005.2:c.38dup XP_006722068.1:p.Thr15AsnfsTer23
XM_011525092.1:c.38dup XP_011523394.1:p.Thr15AsnfsTer23
XM_011525093.1:c.38dup XP_011523395.1:p.Thr15AsnfsTer23
XM_011525094.1:c.38dup XP_011523396.1:p.Thr15AsnfsTer23
XR_934513.1:n.462dup
XR_934514.1:n.462dup
XM_006722001.4:c.389dup XP_006722064.1:p.Thr132AsnfsTer23
XM_006722002.4:c.389dup XP_006722065.1:p.Thr132AsnfsTer23
XM_006722004.3:c.38dup XP_006722067.1:p.Thr15AsnfsTer23
XM_006722005.3:c.38dup XP_006722068.1:p.Thr15AsnfsTer23
XM_011525092.2:c.38dup XP_011523394.1:p.Thr15AsnfsTer23
XM_011525093.2:c.38dup XP_011523395.1:p.Thr15AsnfsTer23
XM_011525094.2:c.38dup XP_011523396.1:p.Thr15AsnfsTer23
XM_017024914.1:c.38dup XP_016880403.1:p.Thr15AsnfsTer23
XM_017024915.1:c.38dup XP_016880404.1:p.Thr15AsnfsTer23
XM_017024916.1:c.38dup XP_016880405.1:p.Thr15AsnfsTer23
XM_017024917.1:c.38dup XP_016880406.1:p.Thr15AsnfsTer23
XM_017024918.2:c.38dup XP_016880407.1:p.Thr15AsnfsTer23
XM_017024919.1:c.38dup XP_016880408.1:p.Thr15AsnfsTer23
XR_934513.3:n.893dup
XR_934514.3:n.893dup
NM_058216.3:c.389dup MANE Select NP_478123.1:p.Thr132AsnfsTer23
NR_103872.2:n.431dup
NM_002876.4:c.389dup NP_002867.1:p.Thr132AsnfsTer7