Canonical Allele Identifier: CA2499224768
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1049265
ClinVar RCV Id: RCV001355171
dbSNP Id: rs2144044038

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732482_58732545del , CM000679.2:g.58732482_58732545del GRCh38
NC_000017.10:g.56809843_56809906del , CM000679.1:g.56809843_56809906del GRCh37
NC_000017.9:g.54164842_54164905del NCBI36
NG_023199.1:g.44881_44944del , LRG_314:g.44881_44944del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.615-2_676del
ENST00000697680.1:c.*1930-2_*1990+1del
ENST00000697681.1:c.*2127-2_*2187+1del
ENST00000697683.1:c.*1902-2_*1962+1del
ENST00000697685.1:c.*1663-2_*1723+1del
ENST00000697686.1:c.737-2_797+1del
ENST00000697689.1:c.*1441-1636_*1441-1573del ENSP00000513398.1:n.*1441-1636_*1441-1573del
ENST00000697690.1:c.905-1636_905-1573del ENSP00000513399.1:n.905-1636_905-1573del
ENST00000697691.1:c.*938-2_*998+1del
ENST00000697692.1:c.*978-2_*1038+1del
ENST00000697694.1:c.615-2_675+1del
ENST00000697695.1:n.1573-2_1633+1del
ENST00000337432.9:c.966-2_1026+1del
ENST00000337432.8:c.966-2_1026+1del
ENST00000413590.5:c.605_667+1del
ENST00000461706.1:n.151_213+1del
ENST00000475762.5:c.*1602-2_*1662+1del
ENST00000482007.5:c.*394-2_*454+1del
ENST00000487525.5:c.*540_*602+1del
ENST00000578151.1:n.240-1636_240-1573del
ENST00000581221.5:n.481-2_541+1del
ENST00000583539.5:c.966-2_1027del
ENST00000584804.1:c.200-2_260+1del
NM_058216.2:c.966-2_1026+1del
NR_103872.1:n.870-2_930+1del
XM_006722001.2:c.967_1029+1del
XM_006722002.2:c.905-2_965+1del
XM_006722004.2:c.616_678+1del
XM_006722005.2:c.616_678+1del
XM_011525092.1:c.616_678+1del
XM_011525093.1:c.616_678+1del
XM_011525094.1:c.616_678+1del
XR_934513.1:n.1184-2_1244+1del
XR_934514.1:n.1185_1247+1del
XR_934886.1:n.149+5526_149+5589del
XM_006722001.4:c.967_1029+1del
XM_006722002.4:c.905-2_965+1del
XM_006722004.3:c.616_678+1del
XM_006722005.3:c.616_678+1del
XM_011525092.2:c.616_678+1del
XM_011525093.2:c.616_678+1del
XM_011525094.2:c.616_678+1del
XM_017024914.1:c.615-2_675+1del
XM_017024915.1:c.615-2_675+1del
XM_017024916.1:c.615-2_675+1del
XM_017024917.1:c.615-2_675+1del
XM_017024918.2:c.615-2_675+1del
XM_017024919.1:c.554-2_614+1del
XR_934513.3:n.1615-2_1675+1del
XR_934514.3:n.1616_1678+1del
XR_934886.2:n.149+5526_149+5589del
NM_058216.3:c.966-2_1026+1del
NR_103872.2:n.841-2_901+1del