Canonical Allele Identifier: CA288629
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 128212
ClinVar RCV Id: RCV000116181 RCV000656963 RCV000696562
dbSNP Id: rs727503760
MyVariant Identifiers: chr17:g.56787355_56787358del (hg19) chr17:g.58709994_58709997del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709994_58709997del , CM000679.2:g.58709994_58709997del GRCh38
NC_000017.10:g.56787355_56787358del , CM000679.1:g.56787355_56787358del GRCh37
NC_000017.9:g.54142354_54142357del NCBI36
NG_023199.1:g.22393_22396del , LRG_314:g.22393_22396del

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.486+4_486+7del ENSP00000464056.2:n.486+4_486+7del
ENST00000697678.1:n.739+4_739+7del
ENST00000697679.1:n.1911+4_1911+7del
ENST00000697680.1:c.*1701+4_*1701+7del ENSP00000513392.1:n.*1701+4_*1701+7del
ENST00000697681.1:c.*1998+4_*1998+7del ENSP00000513393.1:n.*1998+4_*1998+7del
ENST00000697683.1:c.*1701+4_*1701+7del ENSP00000513395.1:n.*1701+4_*1701+7del
ENST00000697684.1:n.897+4_897+7del
ENST00000697685.1:c.*1534+4_*1534+7del ENSP00000513396.1:n.*1534+4_*1534+7del
ENST00000697686.1:c.486+4_486+7del ENSP00000513397.1:n.486+4_486+7del
ENST00000697687.1:n.716+4_716+7del
ENST00000697688.1:n.883+4_883+7del
ENST00000697689.1:c.*1373+4_*1373+7del ENSP00000513398.1:n.*1373+4_*1373+7del
ENST00000697690.1:c.837+4_837+7del ENSP00000513399.1:n.837+4_837+7del
ENST00000697691.1:c.*809+4_*809+7del ENSP00000513400.1:n.*809+4_*809+7del
ENST00000697692.1:c.*849+4_*849+7del ENSP00000513401.1:n.*849+4_*849+7del
ENST00000697694.1:c.486+4_486+7del ENSP00000513402.1:n.486+4_486+7del
ENST00000697695.1:n.1444+4_1444+7del
ENST00000337432.9:c.837+4_837+7del MANE Select ENSP00000336701.4:n.837+4_837+7del
ENST00000337432.8:c.837+4_837+7del ENSP00000336701.4:n.837+4_837+7del
ENST00000413590.5:c.475+4_475+7del
ENST00000475762.5:c.*1540+4_*1540+7del ENSP00000432421.1:n.*1540+4_*1540+7del
ENST00000482007.5:c.*265+4_*265+7del ENSP00000433332.1:n.*265+4_*265+7del
ENST00000487525.5:c.*410+4_*410+7del ENSP00000431637.1:n.*410+4_*410+7del
ENST00000578151.1:n.172+4_172+7del
ENST00000581221.5:n.352+4_352+7del
ENST00000583539.5:c.837+4_837+7del ENSP00000463121.1:n.837+4_837+7del
ENST00000584617.5:c.559+4_559+7del
ENST00000584804.1:c.132+4_132+7del ENSP00000463658.1:n.132+4_132+7del
NM_058216.2:c.837+4_837+7del NP_478123.1:n.837+4_837+7del
NR_103872.1:n.741+4_741+7del
XM_006722001.2:c.837+4_837+7del XP_006722064.1:n.837+4_837+7del
XM_006722002.2:c.837+4_837+7del XP_006722065.1:n.837+4_837+7del
XM_006722004.2:c.486+4_486+7del XP_006722067.1:n.486+4_486+7del
XM_006722005.2:c.486+4_486+7del XP_006722068.1:n.486+4_486+7del
XM_011525092.1:c.486+4_486+7del XP_011523394.1:n.486+4_486+7del
XM_011525093.1:c.486+4_486+7del XP_011523395.1:n.486+4_486+7del
XM_011525094.1:c.486+4_486+7del XP_011523396.1:n.486+4_486+7del
XR_934513.1:n.1055+4_1055+7del
XR_934514.1:n.1055+4_1055+7del
XM_006722001.4:c.837+4_837+7del XP_006722064.1:n.837+4_837+7del
XM_006722002.4:c.837+4_837+7del XP_006722065.1:n.837+4_837+7del
XM_006722004.3:c.486+4_486+7del XP_006722067.1:n.486+4_486+7del
XM_006722005.3:c.486+4_486+7del XP_006722068.1:n.486+4_486+7del
XM_011525092.2:c.486+4_486+7del XP_011523394.1:n.486+4_486+7del
XM_011525093.2:c.486+4_486+7del XP_011523395.1:n.486+4_486+7del
XM_011525094.2:c.486+4_486+7del XP_011523396.1:n.486+4_486+7del
XM_017024914.1:c.486+4_486+7del XP_016880403.1:n.486+4_486+7del
XM_017024915.1:c.486+4_486+7del XP_016880404.1:n.486+4_486+7del
XM_017024916.1:c.486+4_486+7del XP_016880405.1:n.486+4_486+7del
XM_017024917.1:c.486+4_486+7del XP_016880406.1:n.486+4_486+7del
XM_017024918.2:c.486+4_486+7del XP_016880407.1:n.486+4_486+7del
XM_017024919.1:c.486+4_486+7del XP_016880408.1:n.486+4_486+7del
XR_934513.3:n.1486+4_1486+7del
XR_934514.3:n.1486+4_1486+7del
NM_058216.3:c.837+4_837+7del MANE Select NP_478123.1:n.837+4_837+7del
NR_103872.2:n.712+4_712+7del
Search 100 bp 5'
Search 100 bp 3'