Canonical Allele Identifier: CA3261180434
Community Standard Title: NM_058216.3(RAD51C):c.698_699delinsGG (p.His233Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703322_58703323delinsGG , CM000679.2:g.58703322_58703323delinsGG GRCh38
NC_000017.10:g.56780683_56780684delinsGG , CM000679.1:g.56780683_56780684delinsGG GRCh37
NC_000017.9:g.54135682_54135683delinsGG NCBI36
NG_023199.1:g.15721_15722delinsGG , LRG_314:g.15721_15722delinsGG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.698_699delinsGG MANE Select NP_478123.1:p.His233Arg
ENST00000337432.9:c.698_699delinsGG MANE Select ENSP00000336701.4:p.His233Arg
NM_058216.2:c.698_699delinsGG NP_478123.1:p.His233Arg
NR_103872.1:n.602_603delinsGG
NR_103872.2:n.573_574delinsGG
ENST00000337432.8:c.698_699delinsGG ENSP00000336701.4:p.His233Arg
ENST00000413590.5:c.336_337delinsGG
ENST00000425173.5:c.494_495delinsGG ENSP00000407282.1:p.His165Arg
ENST00000461271.5:c.347_348delinsGG ENSP00000464056.1:p.His116Arg
ENST00000461271.6:c.347_348delinsGG ENSP00000464056.2:p.His116Arg
ENST00000475762.5:c.*1401_*1402delinsGG ENSP00000432421.1:n.*1401_*1402delinsGG
ENST00000482007.5:c.*126_*127delinsGG ENSP00000433332.1:n.*126_*127delinsGG
ENST00000487525.5:c.*126_*127delinsGG ENSP00000431637.1:n.*126_*127delinsGG
ENST00000487921.5:n.610_611delinsGG
ENST00000583539.5:c.698_699delinsGG ENSP00000463121.1:p.His233Arg
ENST00000584617.5:c.420_421delinsGG
ENST00000697677.1:n.1779_1780delinsGG
ENST00000697678.1:n.600_601delinsGG
ENST00000697679.1:n.1772_1773delinsGG
ENST00000697680.1:c.*1562_*1563delinsGG ENSP00000513392.1:n.*1562_*1563delinsGG
ENST00000697681.1:c.*1714_*1715delinsGG ENSP00000513393.1:n.*1714_*1715delinsGG
ENST00000697683.1:c.*1562_*1563delinsGG ENSP00000513395.1:n.*1562_*1563delinsGG
ENST00000697684.1:n.758_759delinsGG
ENST00000697685.1:c.*1395_*1396delinsGG ENSP00000513396.1:n.*1395_*1396delinsGG
ENST00000697686.1:c.347_348delinsGG ENSP00000513397.1:p.His116Arg
ENST00000697687.1:n.577_578delinsGG
ENST00000697688.1:n.744_745delinsGG
ENST00000697689.1:c.*1234_*1235delinsGG ENSP00000513398.1:n.*1234_*1235delinsGG
ENST00000697690.1:c.698_699delinsGG ENSP00000513399.1:p.His233Arg
ENST00000697691.1:c.*670_*671delinsGG ENSP00000513400.1:n.*670_*671delinsGG
ENST00000697692.1:c.*710_*711delinsGG ENSP00000513401.1:n.*710_*711delinsGG
ENST00000697694.1:c.347_348delinsGG ENSP00000513402.1:p.His116Arg
ENST00000697695.1:n.1305_1306delinsGG
XM_006722001.2:c.698_699delinsGG XP_006722064.1:p.His233Arg
XM_006722001.4:c.698_699delinsGG XP_006722064.1:p.His233Arg
XM_006722002.2:c.698_699delinsGG XP_006722065.1:p.His233Arg
XM_006722002.4:c.698_699delinsGG XP_006722065.1:p.His233Arg
XM_006722004.2:c.347_348delinsGG XP_006722067.1:p.His116Arg
XM_006722004.3:c.347_348delinsGG XP_006722067.1:p.His116Arg
XM_006722005.2:c.347_348delinsGG XP_006722068.1:p.His116Arg
XM_006722005.3:c.347_348delinsGG XP_006722068.1:p.His116Arg
XM_011525092.1:c.347_348delinsGG XP_011523394.1:p.His116Arg
XM_011525092.2:c.347_348delinsGG XP_011523394.1:p.His116Arg
XM_011525093.1:c.347_348delinsGG XP_011523395.1:p.His116Arg
XM_011525093.2:c.347_348delinsGG XP_011523395.1:p.His116Arg
XM_011525094.1:c.347_348delinsGG XP_011523396.1:p.His116Arg
XM_011525094.2:c.347_348delinsGG XP_011523396.1:p.His116Arg
XM_017024914.1:c.347_348delinsGG XP_016880403.1:p.His116Arg
XM_017024915.1:c.347_348delinsGG XP_016880404.1:p.His116Arg
XM_017024916.1:c.347_348delinsGG XP_016880405.1:p.His116Arg
XM_017024917.1:c.347_348delinsGG XP_016880406.1:p.His116Arg
XM_017024918.2:c.347_348delinsGG XP_016880407.1:p.His116Arg
XM_017024919.1:c.347_348delinsGG XP_016880408.1:p.His116Arg
XR_934513.1:n.771_772delinsGG
XR_934513.3:n.1202_1203delinsGG
XR_934514.1:n.771_772delinsGG
XR_934514.3:n.1202_1203delinsGG