Canonical Allele Identifier: CA3054202745
Gene: RAD51C HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692599_58692710del , CM000679.2:g.58692599_58692710del GRCh38
NC_000017.10:g.56769960_56770071del , CM000679.1:g.56769960_56770071del GRCh37
NC_000017.9:g.54124959_54125070del NCBI36
NG_023199.1:g.4998_5109del , LRG_314:g.4998_5109del
NG_047169.1:g.4371_4482del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-293_-207+25del
ENST00000697675.1:n.27_138del
ENST00000697676.1:n.16_127del
ENST00000697677.1:n.14_125del
ENST00000697678.1:n.14_47+78del
ENST00000697679.1:n.7_118del
ENST00000697680.1:c.-45_67del
ENST00000697681.1:c.-45_67del
ENST00000697683.1:c.-45_67del
ENST00000697684.1:n.16_127del
ENST00000697685.1:c.-45_67del
ENST00000697686.1:c.-240_-207+78del
ENST00000697687.1:n.2_113del
ENST00000697688.1:n.2_113del
ENST00000337432.8:c.-45_67del
ENST00000461271.5:c.-293_-207+25del
ENST00000487921.5:n.24_57+78del
ENST00000583539.5:c.-45_67del
NM_002876.3:c.-45_67del
NM_058216.2:c.-45_67del
NR_103872.1:n.27_138del
NR_103873.1:n.27_113+25del
XM_006722001.2:c.-45_67del
XM_006722002.2:c.-45_67del
XM_006722004.2:c.-293_-207+25del
XM_006722005.2:c.-240_-207+78del
XM_011525092.1:c.-593_-507+25del
XM_011525093.1:c.-754_-668+25del
XR_934513.1:n.29_140del
XR_934514.1:n.29_140del
XM_006722001.4:c.-45_67del
XM_006722002.4:c.-45_67del
XM_006722004.3:c.-293_-207+25del
XM_006722005.3:c.-240_-207+78del
XM_017024914.1:c.-293_-207+25del
XM_017024917.1:c.-240_-207+78del
XR_934513.3:n.460_571del
XR_934514.3:n.460_571del