Canonical Allele Identifier: CA3057243232
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732485_58732486delinsAG , CM000679.2:g.58732485_58732486delinsAG GRCh38
NC_000017.10:g.56809846_56809847delinsAG , CM000679.1:g.56809846_56809847delinsAG GRCh37
NC_000017.9:g.54164845_54164846delinsAG NCBI36
NG_023199.1:g.44884_44885delinsAG , LRG_314:g.44884_44885delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.616_617delinsAG ENSP00000464056.2:p.Leu206Arg
ENST00000697680.1:c.*1931_*1932delinsAG ENSP00000513392.1:n.*1931_*1932delinsAG
ENST00000697681.1:c.*2128_*2129delinsAG ENSP00000513393.1:n.*2128_*2129delinsAG
ENST00000697683.1:c.*1903_*1904delinsAG ENSP00000513395.1:n.*1903_*1904delinsAG
ENST00000697685.1:c.*1664_*1665delinsAG ENSP00000513396.1:n.*1664_*1665delinsAG
ENST00000697686.1:c.738_739delinsAG ENSP00000513397.1:p.Trp247Gly
ENST00000697689.1:c.*1441-1633_*1441-1632delinsAG ENSP00000513398.1:n.*1441-1633_*1441-1632delinsAG
ENST00000697690.1:c.905-1633_905-1632delinsAG ENSP00000513399.1:n.905-1633_905-1632delinsAG
ENST00000697691.1:c.*939_*940delinsAG ENSP00000513400.1:n.*939_*940delinsAG
ENST00000697692.1:c.*979_*980delinsAG ENSP00000513401.1:n.*979_*980delinsAG
ENST00000697694.1:c.616_617delinsAG ENSP00000513402.1:p.Leu206Arg
ENST00000697695.1:n.1574_1575delinsAG
ENST00000337432.9:c.967_968delinsAG MANE Select ENSP00000336701.4:p.Leu323Arg
ENST00000337432.8:c.967_968delinsAG ENSP00000336701.4:p.Leu323Arg
ENST00000413590.5:c.608_609delinsAG
ENST00000461706.1:n.154_155delinsAG
ENST00000475762.5:c.*1603_*1604delinsAG ENSP00000432421.1:n.*1603_*1604delinsAG
ENST00000482007.5:c.*395_*396delinsAG ENSP00000433332.1:n.*395_*396delinsAG
ENST00000487525.5:c.*543_*544delinsAG ENSP00000431637.1:n.*543_*544delinsAG
ENST00000578151.1:n.240-1633_240-1632delinsAG
ENST00000581221.5:n.482_483delinsAG
ENST00000583539.5:c.967_968delinsAG ENSP00000463121.1:p.Leu323Arg
ENST00000584617.5:c.689_690delinsAG
ENST00000584804.1:c.201_202delinsAG ENSP00000463658.1:p.Trp68Gly
NM_058216.2:c.967_968delinsAG NP_478123.1:p.Leu323Arg
NR_103872.1:n.871_872delinsAG
XM_006722001.2:c.970_971delinsAG XP_006722064.1:p.Leu324Arg
XM_006722002.2:c.906_907delinsAG XP_006722065.1:p.Trp303Gly
XM_006722004.2:c.619_620delinsAG XP_006722067.1:p.Leu207Arg
XM_006722005.2:c.619_620delinsAG XP_006722068.1:p.Leu207Arg
XM_011525092.1:c.619_620delinsAG XP_011523394.1:p.Leu207Arg
XM_011525093.1:c.619_620delinsAG XP_011523395.1:p.Leu207Arg
XM_011525094.1:c.619_620delinsAG XP_011523396.1:p.Leu207Arg
XR_934513.1:n.1185_1186delinsAG
XR_934514.1:n.1188_1189delinsAG
XR_934886.1:n.149+5585_149+5586delinsCT
XM_006722001.4:c.970_971delinsAG XP_006722064.1:p.Leu324Arg
XM_006722002.4:c.906_907delinsAG XP_006722065.1:p.Trp303Gly
XM_006722004.3:c.619_620delinsAG XP_006722067.1:p.Leu207Arg
XM_006722005.3:c.619_620delinsAG XP_006722068.1:p.Leu207Arg
XM_011525092.2:c.619_620delinsAG XP_011523394.1:p.Leu207Arg
XM_011525093.2:c.619_620delinsAG XP_011523395.1:p.Leu207Arg
XM_011525094.2:c.619_620delinsAG XP_011523396.1:p.Leu207Arg
XM_017024914.1:c.616_617delinsAG XP_016880403.1:p.Leu206Arg
XM_017024915.1:c.616_617delinsAG XP_016880404.1:p.Leu206Arg
XM_017024916.1:c.616_617delinsAG XP_016880405.1:p.Leu206Arg
XM_017024917.1:c.616_617delinsAG XP_016880406.1:p.Leu206Arg
XM_017024918.2:c.616_617delinsAG XP_016880407.1:p.Leu206Arg
XM_017024919.1:c.555_556delinsAG XP_016880408.1:p.Trp186Gly
XR_934513.3:n.1616_1617delinsAG
XR_934514.3:n.1619_1620delinsAG
XR_934886.2:n.149+5585_149+5586delinsCT
NM_058216.3:c.967_968delinsAG MANE Select NP_478123.1:p.Leu323Arg
NR_103872.2:n.842_843delinsAG