Canonical Allele Identifier: CA916081895

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 854208
• ClinVar RCV Id: RCV001059203

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58699872_58703214del , CM000679.2:g.58699872_58703214del	GRCh38
NC_000017.10:g.56777233_56780575del , CM000679.1:g.56777233_56780575del	GRCh37
NC_000017.9:g.54132232_54135574del	NCBI36
NG_023199.1:g.12271_15613del , LRG_314:g.12271_15613del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.220+3013_239del
ENST00000697677.1:n.1652+3013_1671del
ENST00000697678.1:n.473+3013_492del
ENST00000697679.1:n.1645+3013_1664del
ENST00000697680.1:c.*1435+3013_*1454del
ENST00000697681.1:c.*1463-3_*1606del
ENST00000697683.1:c.*1435+3013_*1454del
ENST00000697684.1:n.631+3013_650del
ENST00000697685.1:c.*1269-3324_*1287del
ENST00000697686.1:c.220+3013_239del
ENST00000697687.1:n.451-3324_469del
ENST00000697688.1:n.617+3013_636del
ENST00000697689.1:c.*1108-3324_*1126del
ENST00000697690.1:c.571+3013_590del
ENST00000697691.1:c.*543+3013_*562del
ENST00000697692.1:c.*583+3013_*602del
ENST00000697694.1:c.220+3013_239del
ENST00000697695.1:n.1178+3013_1197del
ENST00000337432.9:c.571+3013_590del
ENST00000337432.8:c.571+3013_590del
ENST00000413590.5:c.209+3013_228del
ENST00000425173.5:c.367+3013_386del
ENST00000461271.5:c.220+3013_239del
ENST00000475762.5:c.*1274+3013_*1293del
ENST00000482007.5:c.405-3324_*18del
ENST00000487525.5:c.405-3324_*18del
ENST00000487921.5:n.483+3013_502del
ENST00000583539.5:c.571+3013_590del
ENST00000584617.5:c.293+3013_312del
NM_058216.2:c.571+3013_590del
NR_103872.1:n.476-3324_494del
XM_006722001.2:c.571+3013_590del
XM_006722002.2:c.571+3013_590del
XM_006722004.2:c.220+3013_239del
XM_006722005.2:c.220+3013_239del
XM_011525092.1:c.220+3013_239del
XM_011525093.1:c.220+3013_239del
XM_011525094.1:c.220+3013_239del
XR_934513.1:n.644+3013_663del
XR_934514.1:n.644+3013_663del
XM_006722001.4:c.571+3013_590del
XM_006722002.4:c.571+3013_590del
XM_006722004.3:c.220+3013_239del
XM_006722005.3:c.220+3013_239del
XM_011525092.2:c.220+3013_239del
XM_011525093.2:c.220+3013_239del
XM_011525094.2:c.220+3013_239del
XM_017024914.1:c.220+3013_239del
XM_017024915.1:c.220+3013_239del
XM_017024916.1:c.220+3013_239del
XM_017024917.1:c.220+3013_239del
XM_017024918.2:c.220+3013_239del
XM_017024919.1:c.220+3013_239del
XR_934513.3:n.1075+3013_1094del
XR_934514.3:n.1075+3013_1094del
NM_058216.3:c.571+3013_590del
NR_103872.2:n.447-3324_465del