Canonical Allele Identifier: CA3261179372
Community Standard Title: NM_058216.3(RAD51C):c.629_630delinsGA (p.Tyr210Ter)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703253_58703254delinsGA , CM000679.2:g.58703253_58703254delinsGA GRCh38
NC_000017.10:g.56780614_56780615delinsGA , CM000679.1:g.56780614_56780615delinsGA GRCh37
NC_000017.9:g.54135613_54135614delinsGA NCBI36
NG_023199.1:g.15652_15653delinsGA , LRG_314:g.15652_15653delinsGA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.629_630delinsGA MANE Select NP_478123.1:p.Tyr210Ter
ENST00000337432.9:c.629_630delinsGA MANE Select ENSP00000336701.4:p.Tyr210Ter
NM_058216.2:c.629_630delinsGA NP_478123.1:p.Tyr210Ter
NR_103872.1:n.533_534delinsGA
NR_103872.2:n.504_505delinsGA
ENST00000337432.8:c.629_630delinsGA ENSP00000336701.4:p.Tyr210Ter
ENST00000413590.5:c.267_268delinsGA
ENST00000425173.5:c.425_426delinsGA ENSP00000407282.1:p.Tyr142Ter
ENST00000461271.5:c.278_279delinsGA ENSP00000464056.1:p.Tyr93Ter
ENST00000461271.6:c.278_279delinsGA ENSP00000464056.2:p.Tyr93Ter
ENST00000475762.5:c.*1332_*1333delinsGA ENSP00000432421.1:n.*1332_*1333delinsGA
ENST00000482007.5:c.*57_*58delinsGA ENSP00000433332.1:n.*57_*58delinsGA
ENST00000487525.5:c.*57_*58delinsGA ENSP00000431637.1:n.*57_*58delinsGA
ENST00000487921.5:n.541_542delinsGA
ENST00000583539.5:c.629_630delinsGA ENSP00000463121.1:p.Tyr210Ter
ENST00000584617.5:c.351_352delinsGA
ENST00000697677.1:n.1710_1711delinsGA
ENST00000697678.1:n.531_532delinsGA
ENST00000697679.1:n.1703_1704delinsGA
ENST00000697680.1:c.*1493_*1494delinsGA ENSP00000513392.1:n.*1493_*1494delinsGA
ENST00000697681.1:c.*1645_*1646delinsGA ENSP00000513393.1:n.*1645_*1646delinsGA
ENST00000697683.1:c.*1493_*1494delinsGA ENSP00000513395.1:n.*1493_*1494delinsGA
ENST00000697684.1:n.689_690delinsGA
ENST00000697685.1:c.*1326_*1327delinsGA ENSP00000513396.1:n.*1326_*1327delinsGA
ENST00000697686.1:c.278_279delinsGA ENSP00000513397.1:p.Tyr93Ter
ENST00000697687.1:n.508_509delinsGA
ENST00000697688.1:n.675_676delinsGA
ENST00000697689.1:c.*1165_*1166delinsGA ENSP00000513398.1:n.*1165_*1166delinsGA
ENST00000697690.1:c.629_630delinsGA ENSP00000513399.1:p.Tyr210Ter
ENST00000697691.1:c.*601_*602delinsGA ENSP00000513400.1:n.*601_*602delinsGA
ENST00000697692.1:c.*641_*642delinsGA ENSP00000513401.1:n.*641_*642delinsGA
ENST00000697694.1:c.278_279delinsGA ENSP00000513402.1:p.Tyr93Ter
ENST00000697695.1:n.1236_1237delinsGA
XM_006722001.2:c.629_630delinsGA XP_006722064.1:p.Tyr210Ter
XM_006722001.4:c.629_630delinsGA XP_006722064.1:p.Tyr210Ter
XM_006722002.2:c.629_630delinsGA XP_006722065.1:p.Tyr210Ter
XM_006722002.4:c.629_630delinsGA XP_006722065.1:p.Tyr210Ter
XM_006722004.2:c.278_279delinsGA XP_006722067.1:p.Tyr93Ter
XM_006722004.3:c.278_279delinsGA XP_006722067.1:p.Tyr93Ter
XM_006722005.2:c.278_279delinsGA XP_006722068.1:p.Tyr93Ter
XM_006722005.3:c.278_279delinsGA XP_006722068.1:p.Tyr93Ter
XM_011525092.1:c.278_279delinsGA XP_011523394.1:p.Tyr93Ter
XM_011525092.2:c.278_279delinsGA XP_011523394.1:p.Tyr93Ter
XM_011525093.1:c.278_279delinsGA XP_011523395.1:p.Tyr93Ter
XM_011525093.2:c.278_279delinsGA XP_011523395.1:p.Tyr93Ter
XM_011525094.1:c.278_279delinsGA XP_011523396.1:p.Tyr93Ter
XM_011525094.2:c.278_279delinsGA XP_011523396.1:p.Tyr93Ter
XM_017024914.1:c.278_279delinsGA XP_016880403.1:p.Tyr93Ter
XM_017024915.1:c.278_279delinsGA XP_016880404.1:p.Tyr93Ter
XM_017024916.1:c.278_279delinsGA XP_016880405.1:p.Tyr93Ter
XM_017024917.1:c.278_279delinsGA XP_016880406.1:p.Tyr93Ter
XM_017024918.2:c.278_279delinsGA XP_016880407.1:p.Tyr93Ter
XM_017024919.1:c.278_279delinsGA XP_016880408.1:p.Tyr93Ter
XR_934513.1:n.702_703delinsGA
XR_934513.3:n.1133_1134delinsGA
XR_934514.1:n.702_703delinsGA
XR_934514.3:n.1133_1134delinsGA