Canonical Allele Identifier: CA2573055436
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1177646
ClinVar RCV Id: RCV001786496

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692644_58696859del , CM000679.2:g.58692644_58696859del GRCh38
NC_000017.10:g.56770005_56774220del , CM000679.1:g.56770005_56774220del GRCh37
NC_000017.9:g.54125004_54129219del NCBI36
NG_023199.1:g.5043_9258del , LRG_314:g.5043_9258del
NG_047169.1:g.222_4437del

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.-248_220del
ENST00000697675.1:n.72_3168del
ENST00000697676.1:n.61_631del
ENST00000697677.1:n.59_1652del
ENST00000697678.1:n.47+12_473del
ENST00000697679.1:n.52_1645del
ENST00000697680.1:c.1_*1435del
ENST00000697681.1:c.1_*1462del
ENST00000697683.1:c.1_*1435del
ENST00000697684.1:n.61_631del
ENST00000697685.1:c.1_*1268+1670del
ENST00000697686.1:c.-207+12_220del
ENST00000697687.1:n.47_450+1670del
ENST00000697688.1:n.47_617del
ENST00000697689.1:c.1_*1107+1670del
ENST00000697690.1:c.1_571del
ENST00000697691.1:c.1_*543del
ENST00000697692.1:c.1_*583del
ENST00000337432.9:c.1_571del
ENST00000337432.8:c.1_571del
ENST00000461271.5:c.-248_220del
ENST00000475762.5:c.1_*1274del
ENST00000482007.5:c.1_404+1670del
ENST00000487525.5:c.1_404+1670del
ENST00000487921.5:n.57+12_483del
ENST00000583539.5:c.1_571del
NM_058216.2:c.1_571del
NR_103872.1:n.72_475+1670del
XM_006722001.2:c.1_571del
XM_006722002.2:c.1_571del
XM_006722004.2:c.-248_220del
XM_006722005.2:c.-207+12_220del
XM_011525092.1:c.-548_220del
XM_011525093.1:c.-709_220del
XR_934513.1:n.74_644del
XR_934514.1:n.74_644del
XM_006722001.4:c.1_571del
XM_006722002.4:c.1_571del
XM_006722004.3:c.-248_220del
XM_006722005.3:c.-207+12_220del
XM_017024914.1:c.-248_220del
XM_017024916.1:c.-548_220del
XM_017024917.1:c.-207+12_220del
XM_017024918.2:c.-522_220del
XR_934513.3:n.505_1075del
XR_934514.3:n.505_1075del
NM_058216.3:c.1_571del
NR_103872.2:n.43_446+1670del