Canonical Allele Identifier: CA3261179400
Community Standard Title: NM_058216.3(RAD51C):c.629_630delinsGC (p.Tyr210Cys)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703253_58703254delinsGC , CM000679.2:g.58703253_58703254delinsGC GRCh38
NC_000017.10:g.56780614_56780615delinsGC , CM000679.1:g.56780614_56780615delinsGC GRCh37
NC_000017.9:g.54135613_54135614delinsGC NCBI36
NG_023199.1:g.15652_15653delinsGC , LRG_314:g.15652_15653delinsGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.629_630delinsGC MANE Select NP_478123.1:p.Tyr210Cys
ENST00000337432.9:c.629_630delinsGC MANE Select ENSP00000336701.4:p.Tyr210Cys
NM_058216.2:c.629_630delinsGC NP_478123.1:p.Tyr210Cys
NR_103872.1:n.533_534delinsGC
NR_103872.2:n.504_505delinsGC
ENST00000337432.8:c.629_630delinsGC ENSP00000336701.4:p.Tyr210Cys
ENST00000413590.5:c.267_268delinsGC
ENST00000425173.5:c.425_426delinsGC ENSP00000407282.1:p.Tyr142Cys
ENST00000461271.5:c.278_279delinsGC ENSP00000464056.1:p.Tyr93Cys
ENST00000461271.6:c.278_279delinsGC ENSP00000464056.2:p.Tyr93Cys
ENST00000475762.5:c.*1332_*1333delinsGC ENSP00000432421.1:n.*1332_*1333delinsGC
ENST00000482007.5:c.*57_*58delinsGC ENSP00000433332.1:n.*57_*58delinsGC
ENST00000487525.5:c.*57_*58delinsGC ENSP00000431637.1:n.*57_*58delinsGC
ENST00000487921.5:n.541_542delinsGC
ENST00000583539.5:c.629_630delinsGC ENSP00000463121.1:p.Tyr210Cys
ENST00000584617.5:c.351_352delinsGC
ENST00000697677.1:n.1710_1711delinsGC
ENST00000697678.1:n.531_532delinsGC
ENST00000697679.1:n.1703_1704delinsGC
ENST00000697680.1:c.*1493_*1494delinsGC ENSP00000513392.1:n.*1493_*1494delinsGC
ENST00000697681.1:c.*1645_*1646delinsGC ENSP00000513393.1:n.*1645_*1646delinsGC
ENST00000697683.1:c.*1493_*1494delinsGC ENSP00000513395.1:n.*1493_*1494delinsGC
ENST00000697684.1:n.689_690delinsGC
ENST00000697685.1:c.*1326_*1327delinsGC ENSP00000513396.1:n.*1326_*1327delinsGC
ENST00000697686.1:c.278_279delinsGC ENSP00000513397.1:p.Tyr93Cys
ENST00000697687.1:n.508_509delinsGC
ENST00000697688.1:n.675_676delinsGC
ENST00000697689.1:c.*1165_*1166delinsGC ENSP00000513398.1:n.*1165_*1166delinsGC
ENST00000697690.1:c.629_630delinsGC ENSP00000513399.1:p.Tyr210Cys
ENST00000697691.1:c.*601_*602delinsGC ENSP00000513400.1:n.*601_*602delinsGC
ENST00000697692.1:c.*641_*642delinsGC ENSP00000513401.1:n.*641_*642delinsGC
ENST00000697694.1:c.278_279delinsGC ENSP00000513402.1:p.Tyr93Cys
ENST00000697695.1:n.1236_1237delinsGC
XM_006722001.2:c.629_630delinsGC XP_006722064.1:p.Tyr210Cys
XM_006722001.4:c.629_630delinsGC XP_006722064.1:p.Tyr210Cys
XM_006722002.2:c.629_630delinsGC XP_006722065.1:p.Tyr210Cys
XM_006722002.4:c.629_630delinsGC XP_006722065.1:p.Tyr210Cys
XM_006722004.2:c.278_279delinsGC XP_006722067.1:p.Tyr93Cys
XM_006722004.3:c.278_279delinsGC XP_006722067.1:p.Tyr93Cys
XM_006722005.2:c.278_279delinsGC XP_006722068.1:p.Tyr93Cys
XM_006722005.3:c.278_279delinsGC XP_006722068.1:p.Tyr93Cys
XM_011525092.1:c.278_279delinsGC XP_011523394.1:p.Tyr93Cys
XM_011525092.2:c.278_279delinsGC XP_011523394.1:p.Tyr93Cys
XM_011525093.1:c.278_279delinsGC XP_011523395.1:p.Tyr93Cys
XM_011525093.2:c.278_279delinsGC XP_011523395.1:p.Tyr93Cys
XM_011525094.1:c.278_279delinsGC XP_011523396.1:p.Tyr93Cys
XM_011525094.2:c.278_279delinsGC XP_011523396.1:p.Tyr93Cys
XM_017024914.1:c.278_279delinsGC XP_016880403.1:p.Tyr93Cys
XM_017024915.1:c.278_279delinsGC XP_016880404.1:p.Tyr93Cys
XM_017024916.1:c.278_279delinsGC XP_016880405.1:p.Tyr93Cys
XM_017024917.1:c.278_279delinsGC XP_016880406.1:p.Tyr93Cys
XM_017024918.2:c.278_279delinsGC XP_016880407.1:p.Tyr93Cys
XM_017024919.1:c.278_279delinsGC XP_016880408.1:p.Tyr93Cys
XR_934513.1:n.702_703delinsGC
XR_934513.3:n.1133_1134delinsGC
XR_934514.1:n.702_703delinsGC
XR_934514.3:n.1133_1134delinsGC