Canonical Allele Identifier: CA2697560121
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 2774197
ClinVar RCV Id: RCV003585785

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696817_58696827delinsG , CM000679.2:g.58696817_58696827delinsG GRCh38
NC_000017.10:g.56774178_56774188delinsG , CM000679.1:g.56774178_56774188delinsG GRCh37
NC_000017.9:g.54129177_54129187delinsG NCBI36
NG_023199.1:g.9216_9226delinsG , LRG_314:g.9216_9226delinsG
NG_047169.1:g.253_263delinsC

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.178_188delinsG ENSP00000464056.2:p.Ile60ValfsTer4
ENST00000697675.1:n.3126_3136delinsG
ENST00000697676.1:n.589_599delinsG
ENST00000697677.1:n.1610_1620delinsG
ENST00000697678.1:n.431_441delinsG
ENST00000697679.1:n.1603_1613delinsG
ENST00000697680.1:c.*1393_*1403delinsG ENSP00000513392.1:n.*1393_*1403delinsG
ENST00000697681.1:c.*1420_*1430delinsG ENSP00000513393.1:n.*1420_*1430delinsG
ENST00000697683.1:c.*1393_*1403delinsG ENSP00000513395.1:n.*1393_*1403delinsG
ENST00000697684.1:n.589_599delinsG
ENST00000697685.1:c.*1268+1628_*1268+1638delinsG ENSP00000513396.1:n.*1268+1628_*1268+1638...
ENST00000697686.1:c.178_188delinsG ENSP00000513397.1:p.Ile60ValfsTer4
ENST00000697687.1:n.450+1628_450+1638delinsG
ENST00000697688.1:n.575_585delinsG
ENST00000697689.1:c.*1107+1628_*1107+1638delinsG ENSP00000513398.1:n.*1107+1628_*1107+1638...
ENST00000697690.1:c.529_539delinsG ENSP00000513399.1:p.Ile177ValfsTer4
ENST00000697691.1:c.*501_*511delinsG ENSP00000513400.1:n.*501_*511delinsG
ENST00000697692.1:c.*541_*551delinsG ENSP00000513401.1:n.*541_*551delinsG
ENST00000697694.1:c.178_188delinsG ENSP00000513402.1:p.Ile60ValfsTer4
ENST00000697695.1:n.1136_1146delinsG
ENST00000337432.9:c.529_539delinsG MANE Select ENSP00000336701.4:p.Ile177ValfsTer4
ENST00000337432.8:c.529_539delinsG ENSP00000336701.4:p.Ile177ValfsTer4
ENST00000413590.5:c.167_177delinsG
ENST00000425173.5:c.325_335delinsG ENSP00000407282.1:p.Ile109ValfsTer4
ENST00000461271.5:c.178_188delinsG ENSP00000464056.1:p.Ile60ValfsTer4
ENST00000475762.5:c.*1232_*1242delinsG ENSP00000432421.1:n.*1232_*1242delinsG
ENST00000482007.5:c.404+1628_404+1638delinsG ENSP00000433332.1:n.404+1628_404+1638deli...
ENST00000487525.5:c.404+1628_404+1638delinsG ENSP00000431637.1:n.404+1628_404+1638deli...
ENST00000487921.5:n.441_451delinsG
ENST00000583539.5:c.529_539delinsG ENSP00000463121.1:p.Ile177ValfsTer4
ENST00000584617.5:c.251_261delinsG
ENST00000622327.4:c.265_275delinsG ENSP00000482326.1:p.Ile89ValfsTer4
NM_058216.2:c.529_539delinsG NP_478123.1:p.Ile177ValfsTer4
NR_103872.1:n.475+1628_475+1638delinsG
XM_006722001.2:c.529_539delinsG XP_006722064.1:p.Ile177ValfsTer4
XM_006722002.2:c.529_539delinsG XP_006722065.1:p.Ile177ValfsTer4
XM_006722004.2:c.178_188delinsG XP_006722067.1:p.Ile60ValfsTer4
XM_006722005.2:c.178_188delinsG XP_006722068.1:p.Ile60ValfsTer4
XM_011525092.1:c.178_188delinsG XP_011523394.1:p.Ile60ValfsTer4
XM_011525093.1:c.178_188delinsG XP_011523395.1:p.Ile60ValfsTer4
XM_011525094.1:c.178_188delinsG XP_011523396.1:p.Ile60ValfsTer4
XR_934513.1:n.602_612delinsG
XR_934514.1:n.602_612delinsG
XM_006722001.4:c.529_539delinsG XP_006722064.1:p.Ile177ValfsTer4
XM_006722002.4:c.529_539delinsG XP_006722065.1:p.Ile177ValfsTer4
XM_006722004.3:c.178_188delinsG XP_006722067.1:p.Ile60ValfsTer4
XM_006722005.3:c.178_188delinsG XP_006722068.1:p.Ile60ValfsTer4
XM_011525092.2:c.178_188delinsG XP_011523394.1:p.Ile60ValfsTer4
XM_011525093.2:c.178_188delinsG XP_011523395.1:p.Ile60ValfsTer4
XM_011525094.2:c.178_188delinsG XP_011523396.1:p.Ile60ValfsTer4
XM_017024914.1:c.178_188delinsG XP_016880403.1:p.Ile60ValfsTer4
XM_017024915.1:c.178_188delinsG XP_016880404.1:p.Ile60ValfsTer4
XM_017024916.1:c.178_188delinsG XP_016880405.1:p.Ile60ValfsTer4
XM_017024917.1:c.178_188delinsG XP_016880406.1:p.Ile60ValfsTer4
XM_017024918.2:c.178_188delinsG XP_016880407.1:p.Ile60ValfsTer4
XM_017024919.1:c.178_188delinsG XP_016880408.1:p.Ile60ValfsTer4
XR_934513.3:n.1033_1043delinsG
XR_934514.3:n.1033_1043delinsG
NM_058216.3:c.529_539delinsG MANE Select NP_478123.1:p.Ile177ValfsTer4
NR_103872.2:n.446+1628_446+1638delinsG