Canonical Allele Identifier: CA3060598053
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732525_58732526delinsGC , CM000679.2:g.58732525_58732526delinsGC GRCh38
NC_000017.10:g.56809886_56809887delinsGC , CM000679.1:g.56809886_56809887delinsGC GRCh37
NC_000017.9:g.54164885_54164886delinsGC NCBI36
NG_023199.1:g.44924_44925delinsGC , LRG_314:g.44924_44925delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.656_657delinsGC ENSP00000464056.2:p.Thr219Ser
ENST00000697680.1:c.*1971_*1972delinsGC ENSP00000513392.1:n.*1971_*1972delinsGC
ENST00000697681.1:c.*2168_*2169delinsGC ENSP00000513393.1:n.*2168_*2169delinsGC
ENST00000697683.1:c.*1943_*1944delinsGC ENSP00000513395.1:n.*1943_*1944delinsGC
ENST00000697685.1:c.*1704_*1705delinsGC ENSP00000513396.1:n.*1704_*1705delinsGC
ENST00000697686.1:c.778_779delinsGC ENSP00000513397.1:p.Gln260Ala
ENST00000697689.1:c.*1441-1593_*1441-1592delinsGC ENSP00000513398.1:n.*1441-1593_*1441-1592delinsGC
ENST00000697690.1:c.905-1593_905-1592delinsGC ENSP00000513399.1:n.905-1593_905-1592delinsGC
ENST00000697691.1:c.*979_*980delinsGC ENSP00000513400.1:n.*979_*980delinsGC
ENST00000697692.1:c.*1019_*1020delinsGC ENSP00000513401.1:n.*1019_*1020delinsGC
ENST00000697694.1:c.656_657delinsGC ENSP00000513402.1:p.Thr219Ser
ENST00000697695.1:n.1614_1615delinsGC
ENST00000337432.9:c.1007_1008delinsGC MANE Select ENSP00000336701.4:p.Thr336Ser
ENST00000337432.8:c.1007_1008delinsGC ENSP00000336701.4:p.Thr336Ser
ENST00000413590.5:c.648_649delinsGC
ENST00000461706.1:n.194_195delinsGC
ENST00000475762.5:c.*1643_*1644delinsGC ENSP00000432421.1:n.*1643_*1644delinsGC
ENST00000482007.5:c.*435_*436delinsGC ENSP00000433332.1:n.*435_*436delinsGC
ENST00000487525.5:c.*583_*584delinsGC ENSP00000431637.1:n.*583_*584delinsGC
ENST00000578151.1:n.240-1593_240-1592delinsGC
ENST00000581221.5:n.522_523delinsGC
ENST00000583539.5:c.1007_1008delinsGC ENSP00000463121.1:p.Thr336Ser
ENST00000584804.1:c.241_242delinsGC ENSP00000463658.1:p.Gln81Ala
NM_058216.2:c.1007_1008delinsGC NP_478123.1:p.Thr336Ser
NR_103872.1:n.911_912delinsGC
XM_006722001.2:c.1010_1011delinsGC XP_006722064.1:p.Thr337Ser
XM_006722002.2:c.946_947delinsGC XP_006722065.1:p.Gln316Ala
XM_006722004.2:c.659_660delinsGC XP_006722067.1:p.Thr220Ser
XM_006722005.2:c.659_660delinsGC XP_006722068.1:p.Thr220Ser
XM_011525092.1:c.659_660delinsGC XP_011523394.1:p.Thr220Ser
XM_011525093.1:c.659_660delinsGC XP_011523395.1:p.Thr220Ser
XM_011525094.1:c.659_660delinsGC XP_011523396.1:p.Thr220Ser
XR_934513.1:n.1225_1226delinsGC
XR_934514.1:n.1228_1229delinsGC
XR_934886.1:n.149+5545_149+5546delinsGC
XM_006722001.4:c.1010_1011delinsGC XP_006722064.1:p.Thr337Ser
XM_006722002.4:c.946_947delinsGC XP_006722065.1:p.Gln316Ala
XM_006722004.3:c.659_660delinsGC XP_006722067.1:p.Thr220Ser
XM_006722005.3:c.659_660delinsGC XP_006722068.1:p.Thr220Ser
XM_011525092.2:c.659_660delinsGC XP_011523394.1:p.Thr220Ser
XM_011525093.2:c.659_660delinsGC XP_011523395.1:p.Thr220Ser
XM_011525094.2:c.659_660delinsGC XP_011523396.1:p.Thr220Ser
XM_017024914.1:c.656_657delinsGC XP_016880403.1:p.Thr219Ser
XM_017024915.1:c.656_657delinsGC XP_016880404.1:p.Thr219Ser
XM_017024916.1:c.656_657delinsGC XP_016880405.1:p.Thr219Ser
XM_017024917.1:c.656_657delinsGC XP_016880406.1:p.Thr219Ser
XM_017024918.2:c.656_657delinsGC XP_016880407.1:p.Thr219Ser
XM_017024919.1:c.595_596delinsGC XP_016880408.1:p.Gln199Ala
XR_934513.3:n.1656_1657delinsGC
XR_934514.3:n.1659_1660delinsGC
XR_934886.2:n.149+5545_149+5546delinsGC
NM_058216.3:c.1007_1008delinsGC MANE Select NP_478123.1:p.Thr336Ser
NR_103872.2:n.882_883delinsGC