Canonical Allele Identifier: CA3057228378
Community Standard Title: NM_058216.3(RAD51C):c.828_830delinsTAC (p.Arg277Thr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709981_58709983delinsTAC , CM000679.2:g.58709981_58709983delinsTAC GRCh38
NC_000017.10:g.56787342_56787344delinsTAC , CM000679.1:g.56787342_56787344delinsTAC GRCh37
NC_000017.9:g.54142341_54142343delinsTAC NCBI36
NG_023199.1:g.22380_22382delinsTAC , LRG_314:g.22380_22382delinsTAC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.828_830delinsTAC MANE Select NP_478123.1:p.Arg277Thr
ENST00000337432.9:c.828_830delinsTAC MANE Select ENSP00000336701.4:p.Arg277Thr
NM_058216.2:c.828_830delinsTAC NP_478123.1:p.Arg277Thr
NR_103872.1:n.732_734delinsTAC
NR_103872.2:n.703_705delinsTAC
ENST00000337432.8:c.828_830delinsTAC ENSP00000336701.4:p.Arg277Thr
ENST00000413590.5:c.466_468delinsTAC
ENST00000461271.6:c.477_479delinsTAC ENSP00000464056.2:p.Arg160Thr
ENST00000475762.5:c.*1531_*1533delinsTAC ENSP00000432421.1:n.*1531_*1533delinsTAC
ENST00000482007.5:c.*256_*258delinsTAC ENSP00000433332.1:n.*256_*258delinsTAC
ENST00000487525.5:c.*401_*403delinsTAC ENSP00000431637.1:n.*401_*403delinsTAC
ENST00000578151.1:n.163_165delinsTAC
ENST00000581221.5:n.343_345delinsTAC
ENST00000583539.5:c.828_830delinsTAC ENSP00000463121.1:p.Arg277Thr
ENST00000584617.5:c.550_552delinsTAC
ENST00000584804.1:c.123_125delinsTAC ENSP00000463658.1:p.Arg42Thr
ENST00000697678.1:n.730_732delinsTAC
ENST00000697679.1:n.1902_1904delinsTAC
ENST00000697680.1:c.*1692_*1694delinsTAC ENSP00000513392.1:n.*1692_*1694delinsTAC
ENST00000697681.1:c.*1989_*1991delinsTAC ENSP00000513393.1:n.*1989_*1991delinsTAC
ENST00000697683.1:c.*1692_*1694delinsTAC ENSP00000513395.1:n.*1692_*1694delinsTAC
ENST00000697684.1:n.888_890delinsTAC
ENST00000697685.1:c.*1525_*1527delinsTAC ENSP00000513396.1:n.*1525_*1527delinsTAC
ENST00000697686.1:c.477_479delinsTAC ENSP00000513397.1:p.Arg160Thr
ENST00000697687.1:n.707_709delinsTAC
ENST00000697688.1:n.874_876delinsTAC
ENST00000697689.1:c.*1364_*1366delinsTAC ENSP00000513398.1:n.*1364_*1366delinsTAC
ENST00000697690.1:c.828_830delinsTAC ENSP00000513399.1:p.Arg277Thr
ENST00000697691.1:c.*800_*802delinsTAC ENSP00000513400.1:n.*800_*802delinsTAC
ENST00000697692.1:c.*840_*842delinsTAC ENSP00000513401.1:n.*840_*842delinsTAC
ENST00000697694.1:c.477_479delinsTAC ENSP00000513402.1:p.Arg160Thr
ENST00000697695.1:n.1435_1437delinsTAC
XM_006722001.2:c.828_830delinsTAC XP_006722064.1:p.Arg277Thr
XM_006722001.4:c.828_830delinsTAC XP_006722064.1:p.Arg277Thr
XM_006722002.2:c.828_830delinsTAC XP_006722065.1:p.Arg277Thr
XM_006722002.4:c.828_830delinsTAC XP_006722065.1:p.Arg277Thr
XM_006722004.2:c.477_479delinsTAC XP_006722067.1:p.Arg160Thr
XM_006722004.3:c.477_479delinsTAC XP_006722067.1:p.Arg160Thr
XM_006722005.2:c.477_479delinsTAC XP_006722068.1:p.Arg160Thr
XM_006722005.3:c.477_479delinsTAC XP_006722068.1:p.Arg160Thr
XM_011525092.1:c.477_479delinsTAC XP_011523394.1:p.Arg160Thr
XM_011525092.2:c.477_479delinsTAC XP_011523394.1:p.Arg160Thr
XM_011525093.1:c.477_479delinsTAC XP_011523395.1:p.Arg160Thr
XM_011525093.2:c.477_479delinsTAC XP_011523395.1:p.Arg160Thr
XM_011525094.1:c.477_479delinsTAC XP_011523396.1:p.Arg160Thr
XM_011525094.2:c.477_479delinsTAC XP_011523396.1:p.Arg160Thr
XM_017024914.1:c.477_479delinsTAC XP_016880403.1:p.Arg160Thr
XM_017024915.1:c.477_479delinsTAC XP_016880404.1:p.Arg160Thr
XM_017024916.1:c.477_479delinsTAC XP_016880405.1:p.Arg160Thr
XM_017024917.1:c.477_479delinsTAC XP_016880406.1:p.Arg160Thr
XM_017024918.2:c.477_479delinsTAC XP_016880407.1:p.Arg160Thr
XM_017024919.1:c.477_479delinsTAC XP_016880408.1:p.Arg160Thr
XR_934513.1:n.1046_1048delinsTAC
XR_934513.3:n.1477_1479delinsTAC
XR_934514.1:n.1046_1048delinsTAC
XR_934514.3:n.1477_1479delinsTAC