Canonical Allele Identifier: CA3057243463
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732532_58732534delinsACC , CM000679.2:g.58732532_58732534delinsACC GRCh38
NC_000017.10:g.56809893_56809895delinsACC , CM000679.1:g.56809893_56809895delinsACC GRCh37
NC_000017.9:g.54164892_54164894delinsACC NCBI36
NG_023199.1:g.44931_44933delinsACC , LRG_314:g.44931_44933delinsACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.663_665delinsACC ENSP00000464056.2:p.Phe222Pro
ENST00000697680.1:c.*1978_*1980delinsACC ENSP00000513392.1:n.*1978_*1980delinsACC
ENST00000697681.1:c.*2175_*2177delinsACC ENSP00000513393.1:n.*2175_*2177delinsACC
ENST00000697683.1:c.*1950_*1952delinsACC ENSP00000513395.1:n.*1950_*1952delinsACC
ENST00000697685.1:c.*1711_*1713delinsACC ENSP00000513396.1:n.*1711_*1713delinsACC
ENST00000697686.1:c.785_787delinsACC ENSP00000513397.1:p.Cys262_Phe263delinsTyrLeu
ENST00000697689.1:c.*1441-1586_*1441-1584delinsACC ENSP00000513398.1:n.*1441-1586_*1441-1584delinsACC
ENST00000697690.1:c.905-1586_905-1584delinsACC ENSP00000513399.1:n.905-1586_905-1584delinsACC
ENST00000697691.1:c.*986_*988delinsACC ENSP00000513400.1:n.*986_*988delinsACC
ENST00000697692.1:c.*1026_*1028delinsACC ENSP00000513401.1:n.*1026_*1028delinsACC
ENST00000697694.1:c.663_665delinsACC ENSP00000513402.1:p.Phe222Pro
ENST00000697695.1:n.1621_1623delinsACC
ENST00000337432.9:c.1014_1016delinsACC MANE Select ENSP00000336701.4:p.Phe339Pro
ENST00000337432.8:c.1014_1016delinsACC ENSP00000336701.4:p.Phe339Pro
ENST00000413590.5:c.655_657delinsACC
ENST00000461706.1:n.201_203delinsACC
ENST00000475762.5:c.*1650_*1652delinsACC ENSP00000432421.1:n.*1650_*1652delinsACC
ENST00000482007.5:c.*442_*444delinsACC ENSP00000433332.1:n.*442_*444delinsACC
ENST00000487525.5:c.*590_*592delinsACC ENSP00000431637.1:n.*590_*592delinsACC
ENST00000578151.1:n.240-1586_240-1584delinsACC
ENST00000581221.5:n.529_531delinsACC
ENST00000583539.5:c.1014_1016delinsACC ENSP00000463121.1:p.Phe339Pro
ENST00000584804.1:c.248_250delinsACC ENSP00000463658.1:p.Cys83_Phe84delinsTyrLeu
NM_058216.2:c.1014_1016delinsACC NP_478123.1:p.Phe339Pro
NR_103872.1:n.918_920delinsACC
XM_006722001.2:c.1017_1019delinsACC XP_006722064.1:p.Phe340Pro
XM_006722002.2:c.953_955delinsACC XP_006722065.1:p.Cys318_Phe319delinsTyrLeu
XM_006722004.2:c.666_668delinsACC XP_006722067.1:p.Phe223Pro
XM_006722005.2:c.666_668delinsACC XP_006722068.1:p.Phe223Pro
XM_011525092.1:c.666_668delinsACC XP_011523394.1:p.Phe223Pro
XM_011525093.1:c.666_668delinsACC XP_011523395.1:p.Phe223Pro
XM_011525094.1:c.666_668delinsACC XP_011523396.1:p.Phe223Pro
XR_934513.1:n.1232_1234delinsACC
XR_934514.1:n.1235_1237delinsACC
XR_934886.1:n.149+5537_149+5539delinsGGT
XM_006722001.4:c.1017_1019delinsACC XP_006722064.1:p.Phe340Pro
XM_006722002.4:c.953_955delinsACC XP_006722065.1:p.Cys318_Phe319delinsTyrLeu
XM_006722004.3:c.666_668delinsACC XP_006722067.1:p.Phe223Pro
XM_006722005.3:c.666_668delinsACC XP_006722068.1:p.Phe223Pro
XM_011525092.2:c.666_668delinsACC XP_011523394.1:p.Phe223Pro
XM_011525093.2:c.666_668delinsACC XP_011523395.1:p.Phe223Pro
XM_011525094.2:c.666_668delinsACC XP_011523396.1:p.Phe223Pro
XM_017024914.1:c.663_665delinsACC XP_016880403.1:p.Phe222Pro
XM_017024915.1:c.663_665delinsACC XP_016880404.1:p.Phe222Pro
XM_017024916.1:c.663_665delinsACC XP_016880405.1:p.Phe222Pro
XM_017024917.1:c.663_665delinsACC XP_016880406.1:p.Phe222Pro
XM_017024918.2:c.663_665delinsACC XP_016880407.1:p.Phe222Pro
XM_017024919.1:c.602_604delinsACC XP_016880408.1:p.Cys201_Phe202delinsTyrLeu
XR_934513.3:n.1663_1665delinsACC
XR_934514.3:n.1666_1668delinsACC
XR_934886.2:n.149+5537_149+5539delinsGGT
NM_058216.3:c.1014_1016delinsACC MANE Select NP_478123.1:p.Phe339Pro
NR_103872.2:n.889_891delinsACC