Canonical Allele Identifier: CA773571855
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs1170424948

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692590_58692593del , CM000679.2:g.58692590_58692593del GRCh38
NC_000017.10:g.56769951_56769954del , CM000679.1:g.56769951_56769954del GRCh37
NC_000017.9:g.54124950_54124953del NCBI36
NG_023199.1:g.4989_4992del , LRG_314:g.4989_4992del
NG_047169.1:g.4487_4490del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-302_-299del ENSP00000464056.2:n.-302_-299del
ENST00000697675.1:n.18_21del
ENST00000697676.1:n.7_10del
ENST00000697677.1:n.5_8del
ENST00000697678.1:n.5_8del
ENST00000697683.1:c.-54_-51del ENSP00000513395.1:n.-54_-51del
ENST00000697684.1:n.7_10del
ENST00000337432.8:c.-54_-51del ENSP00000336701.4:n.-54_-51del
ENST00000461271.5:c.-302_-299del ENSP00000464056.1:n.-302_-299del
ENST00000487921.5:n.15_18del
ENST00000583539.5:c.-54_-51del ENSP00000463121.1:n.-54_-51del
NM_002876.3:c.-54_-51del NP_002867.1:n.-54_-51del
NM_058216.2:c.-54_-51del NP_478123.1:n.-54_-51del
NR_103872.1:n.18_21del
NR_103873.1:n.18_21del
XM_006722001.2:c.-54_-51del XP_006722064.1:n.-54_-51del
XM_006722002.2:c.-54_-51del XP_006722065.1:n.-54_-51del
XM_006722004.2:c.-302_-299del XP_006722067.1:n.-302_-299del
XM_006722005.2:c.-249_-246del XP_006722068.1:n.-249_-246del
XM_011525092.1:c.-602_-599del XP_011523394.1:n.-602_-599del
XM_011525093.1:c.-763_-760del XP_011523395.1:n.-763_-760del
XR_934513.1:n.20_23del
XR_934514.1:n.20_23del
XM_006722001.4:c.-54_-51del XP_006722064.1:n.-54_-51del
XM_006722002.4:c.-54_-51del XP_006722065.1:n.-54_-51del
XM_006722004.3:c.-302_-299del XP_006722067.1:n.-302_-299del
XM_006722005.3:c.-249_-246del XP_006722068.1:n.-249_-246del
XM_017024914.1:c.-302_-299del XP_016880403.1:n.-302_-299del
XM_017024917.1:c.-249_-246del XP_016880406.1:n.-249_-246del
XR_934513.3:n.451_454del
XR_934514.3:n.451_454del