Canonical Allele Identifier: CA2267813907
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692583_58692606delinsCGCACGCCCCAGCGAGGGCGTGCG , CM000679.2:g.58692583_58692606delinsCGCACGCCCCAGCGAGGGCGTGCG GRCh38
NC_000017.10:g.56769944_56769967delinsCGCACGCCCCAGCGAGGGCGTGCG , CM000679.1:g.56769944_56769967delinsCGCACGCCCCAGCGAGGGCGTGCG GRCh37
NC_000017.9:g.54124943_54124966delinsCGCACGCCCCAGCGAGGGCGTGCG NCBI36
NG_023199.1:g.4982_5005delinsCGCACGCCCCAGCGAGGGCGTGCG , LRG_314:g.4982_5005delinsCGCACGCCCCAGCGAGGGCGTGCG
NG_047169.1:g.4474_4497delinsCGCACGCCCTCGCTGGGGCGTGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-309_-286delinsCGCACGCCCCAGCGAGGGCGTGCG ENSP00000464056.2:n.-309_-286delinsCGCACGCCCCAGCGAGGGCGTGCG
ENST00000697675.1:n.11_34delinsCGCACGCCCCAGCGAGGGCGTGCG
ENST00000697683.1:c.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG ENSP00000513395.1:n.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG
ENST00000337432.8:c.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG ENSP00000336701.4:n.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG
ENST00000461271.5:c.-309_-286delinsCGCACGCCCCAGCGAGGGCGTGCG ENSP00000464056.1:n.-309_-286delinsCGCACGCCCCAGCGAGGGCGTGCG
ENST00000487921.5:n.8_31delinsCGCACGCCCCAGCGAGGGCGTGCG
ENST00000583539.5:c.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG ENSP00000463121.1:n.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG
NM_002876.3:c.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG NP_002867.1:n.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG
NM_058216.2:c.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG NP_478123.1:n.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG
NR_103872.1:n.11_34delinsCGCACGCCCCAGCGAGGGCGTGCG
NR_103873.1:n.11_34delinsCGCACGCCCCAGCGAGGGCGTGCG
XM_006722001.2:c.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG XP_006722064.1:n.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG
XM_006722002.2:c.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG XP_006722065.1:n.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG
XM_006722004.2:c.-309_-286delinsCGCACGCCCCAGCGAGGGCGTGCG XP_006722067.1:n.-309_-286delinsCGCACGCCCCAGCGAGGGCGTGCG
XM_006722005.2:c.-256_-233delinsCGCACGCCCCAGCGAGGGCGTGCG XP_006722068.1:n.-256_-233delinsCGCACGCCCCAGCGAGGGCGTGCG
XR_934513.1:n.13_36delinsCGCACGCCCCAGCGAGGGCGTGCG
XR_934514.1:n.13_36delinsCGCACGCCCCAGCGAGGGCGTGCG
XM_006722001.4:c.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG XP_006722064.1:n.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG
XM_006722002.4:c.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG XP_006722065.1:n.-61_-38delinsCGCACGCCCCAGCGAGGGCGTGCG
XM_006722004.3:c.-309_-286delinsCGCACGCCCCAGCGAGGGCGTGCG XP_006722067.1:n.-309_-286delinsCGCACGCCCCAGCGAGGGCGTGCG
XM_006722005.3:c.-256_-233delinsCGCACGCCCCAGCGAGGGCGTGCG XP_006722068.1:n.-256_-233delinsCGCACGCCCCAGCGAGGGCGTGCG
XM_017024914.1:c.-309_-286delinsCGCACGCCCCAGCGAGGGCGTGCG XP_016880403.1:n.-309_-286delinsCGCACGCCCCAGCGAGGGCGTGCG
XM_017024917.1:c.-256_-233delinsCGCACGCCCCAGCGAGGGCGTGCG XP_016880406.1:n.-256_-233delinsCGCACGCCCCAGCGAGGGCGTGCG
XR_934513.3:n.444_467delinsCGCACGCCCCAGCGAGGGCGTGCG
XR_934514.3:n.444_467delinsCGCACGCCCCAGCGAGGGCGTGCG