Canonical Allele Identifier: CA3261180536
Community Standard Title: NM_058216.3(RAD51C):c.830_831delinsCC (p.Arg277Thr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709983_58709984delinsCC , CM000679.2:g.58709983_58709984delinsCC GRCh38
NC_000017.10:g.56787344_56787345delinsCC , CM000679.1:g.56787344_56787345delinsCC GRCh37
NC_000017.9:g.54142343_54142344delinsCC NCBI36
NG_023199.1:g.22382_22383delinsCC , LRG_314:g.22382_22383delinsCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.830_831delinsCC MANE Select NP_478123.1:p.Arg277Thr
ENST00000337432.9:c.830_831delinsCC MANE Select ENSP00000336701.4:p.Arg277Thr
NM_058216.2:c.830_831delinsCC NP_478123.1:p.Arg277Thr
NR_103872.1:n.734_735delinsCC
NR_103872.2:n.705_706delinsCC
ENST00000337432.8:c.830_831delinsCC ENSP00000336701.4:p.Arg277Thr
ENST00000413590.5:c.468_469delinsCC
ENST00000461271.6:c.479_480delinsCC ENSP00000464056.2:p.Arg160Thr
ENST00000475762.5:c.*1533_*1534delinsCC ENSP00000432421.1:n.*1533_*1534delinsCC
ENST00000482007.5:c.*258_*259delinsCC ENSP00000433332.1:n.*258_*259delinsCC
ENST00000487525.5:c.*403_*404delinsCC ENSP00000431637.1:n.*403_*404delinsCC
ENST00000578151.1:n.165_166delinsCC
ENST00000581221.5:n.345_346delinsCC
ENST00000583539.5:c.830_831delinsCC ENSP00000463121.1:p.Arg277Thr
ENST00000584617.5:c.552_553delinsCC
ENST00000584804.1:c.125_126delinsCC ENSP00000463658.1:p.Arg42Thr
ENST00000697678.1:n.732_733delinsCC
ENST00000697679.1:n.1904_1905delinsCC
ENST00000697680.1:c.*1694_*1695delinsCC ENSP00000513392.1:n.*1694_*1695delinsCC
ENST00000697681.1:c.*1991_*1992delinsCC ENSP00000513393.1:n.*1991_*1992delinsCC
ENST00000697683.1:c.*1694_*1695delinsCC ENSP00000513395.1:n.*1694_*1695delinsCC
ENST00000697684.1:n.890_891delinsCC
ENST00000697685.1:c.*1527_*1528delinsCC ENSP00000513396.1:n.*1527_*1528delinsCC
ENST00000697686.1:c.479_480delinsCC ENSP00000513397.1:p.Arg160Thr
ENST00000697687.1:n.709_710delinsCC
ENST00000697688.1:n.876_877delinsCC
ENST00000697689.1:c.*1366_*1367delinsCC ENSP00000513398.1:n.*1366_*1367delinsCC
ENST00000697690.1:c.830_831delinsCC ENSP00000513399.1:p.Arg277Thr
ENST00000697691.1:c.*802_*803delinsCC ENSP00000513400.1:n.*802_*803delinsCC
ENST00000697692.1:c.*842_*843delinsCC ENSP00000513401.1:n.*842_*843delinsCC
ENST00000697694.1:c.479_480delinsCC ENSP00000513402.1:p.Arg160Thr
ENST00000697695.1:n.1437_1438delinsCC
XM_006722001.2:c.830_831delinsCC XP_006722064.1:p.Arg277Thr
XM_006722001.4:c.830_831delinsCC XP_006722064.1:p.Arg277Thr
XM_006722002.2:c.830_831delinsCC XP_006722065.1:p.Arg277Thr
XM_006722002.4:c.830_831delinsCC XP_006722065.1:p.Arg277Thr
XM_006722004.2:c.479_480delinsCC XP_006722067.1:p.Arg160Thr
XM_006722004.3:c.479_480delinsCC XP_006722067.1:p.Arg160Thr
XM_006722005.2:c.479_480delinsCC XP_006722068.1:p.Arg160Thr
XM_006722005.3:c.479_480delinsCC XP_006722068.1:p.Arg160Thr
XM_011525092.1:c.479_480delinsCC XP_011523394.1:p.Arg160Thr
XM_011525092.2:c.479_480delinsCC XP_011523394.1:p.Arg160Thr
XM_011525093.1:c.479_480delinsCC XP_011523395.1:p.Arg160Thr
XM_011525093.2:c.479_480delinsCC XP_011523395.1:p.Arg160Thr
XM_011525094.1:c.479_480delinsCC XP_011523396.1:p.Arg160Thr
XM_011525094.2:c.479_480delinsCC XP_011523396.1:p.Arg160Thr
XM_017024914.1:c.479_480delinsCC XP_016880403.1:p.Arg160Thr
XM_017024915.1:c.479_480delinsCC XP_016880404.1:p.Arg160Thr
XM_017024916.1:c.479_480delinsCC XP_016880405.1:p.Arg160Thr
XM_017024917.1:c.479_480delinsCC XP_016880406.1:p.Arg160Thr
XM_017024918.2:c.479_480delinsCC XP_016880407.1:p.Arg160Thr
XM_017024919.1:c.479_480delinsCC XP_016880408.1:p.Arg160Thr
XR_934513.1:n.1048_1049delinsCC
XR_934513.3:n.1479_1480delinsCC
XR_934514.1:n.1048_1049delinsCC
XR_934514.3:n.1479_1480delinsCC