Canonical Allele Identifier: CA333752
Gene: RAD51C HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 182844
dbSNP Id: rs730881939

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695009dup , CM000679.2:g.58695009dup GRCh38
NC_000017.10:g.56772370dup , CM000679.1:g.56772370dup GRCh37
NC_000017.9:g.54127369dup NCBI36
NG_023199.1:g.7408dup , LRG_314:g.7408dup
NG_047169.1:g.2071dup

Transcript Alleles

HGVS Amino-acid change
NM_002876.3:c.224dup VV NP_002867.1:p.Tyr75Ter
NM_058216.2:c.224dup VV NP_478123.1:p.Tyr75Ter
NR_103872.1:n.295dup
NR_103873.1:n.192dup
XM_006722001.2:c.224dup XP_006722064.1:p.Tyr75Ter
XM_006722002.2:c.224dup XP_006722065.1:p.Tyr75Ter
XM_006722004.2:c.-128dup XP_006722067.1:p.=
XM_006722005.2:c.-128dup XP_006722068.1:p.=
XM_011525092.1:c.-128dup XP_011523394.1:p.=
XM_011525093.1:c.-128dup XP_011523395.1:p.=
XM_011525094.1:c.-128dup XP_011523396.1:p.=
XR_934513.1:n.297dup
XR_934514.1:n.297dup
XM_006722001.4:c.224dup XP_006722064.1:p.Tyr75Ter
XM_006722002.4:c.224dup XP_006722065.1:p.Tyr75Ter
XM_006722004.3:c.-128dup XP_006722067.1:p.=
XM_006722005.3:c.-128dup XP_006722068.1:p.=
XM_011525092.2:c.-128dup XP_011523394.1:p.=
XM_011525093.2:c.-128dup XP_011523395.1:p.=
XM_011525094.2:c.-128dup XP_011523396.1:p.=
XM_017024914.1:c.-128dup XP_016880403.1:p.=
XM_017024915.1:c.-128dup XP_016880404.1:p.=
XM_017024916.1:c.-128dup XP_016880405.1:p.=
XM_017024917.1:c.-128dup XP_016880406.1:p.=
XM_017024918.2:c.-128dup XP_016880407.1:p.=
XM_017024919.1:c.-128dup XP_016880408.1:p.=
XR_934513.3:n.728dup
XR_934514.3:n.728dup
NM_058216.3:c.224dup VV MANE Preferred NP_478123.1:p.Tyr75Ter
ENST00000337432.8:c.224dup ENSP00000336701.4:p.Tyr75Ter
ENST00000421782.3:c.224dup ENSP00000391450.2:p.Tyr75Ter
ENST00000425173.5:n.20dup ENSP00000407282.1:p.Tyr7Ter
ENST00000461271.5:c.-128dup ENSP00000464056.1:p.=
ENST00000475762.5:c.*927dup ENSP00000432421.1:p.=
ENST00000482007.5:c.224dup ENSP00000433332.1:p.Tyr75Ter
ENST00000486827.1:c.*1088dup ENSP00000436761.1:p.=
ENST00000487525.5:c.224dup ENSP00000431637.1:p.Tyr75Ter
ENST00000487921.5:n.136dup
ENST00000583539.5:c.224dup ENSP00000463121.1:p.Tyr75Ter
ENST00000584617.5:n.127-1684dup