Canonical Allele Identifier: CA3261179317
Community Standard Title: NM_058216.3(RAD51C):c.749_750delinsGG (p.His250Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709902_58709903delinsGG , CM000679.2:g.58709902_58709903delinsGG GRCh38
NC_000017.10:g.56787263_56787264delinsGG , CM000679.1:g.56787263_56787264delinsGG GRCh37
NC_000017.9:g.54142262_54142263delinsGG NCBI36
NG_023199.1:g.22301_22302delinsGG , LRG_314:g.22301_22302delinsGG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.749_750delinsGG MANE Select NP_478123.1:p.His250Arg
ENST00000337432.9:c.749_750delinsGG MANE Select ENSP00000336701.4:p.His250Arg
NM_058216.2:c.749_750delinsGG NP_478123.1:p.His250Arg
NR_103872.1:n.653_654delinsGG
NR_103872.2:n.624_625delinsGG
ENST00000337432.8:c.749_750delinsGG ENSP00000336701.4:p.His250Arg
ENST00000413590.5:c.387_388delinsGG
ENST00000461271.5:c.398_399delinsGG ENSP00000464056.1:p.His133Arg
ENST00000461271.6:c.398_399delinsGG ENSP00000464056.2:p.His133Arg
ENST00000475762.5:c.*1452_*1453delinsGG ENSP00000432421.1:n.*1452_*1453delinsGG
ENST00000482007.5:c.*177_*178delinsGG ENSP00000433332.1:n.*177_*178delinsGG
ENST00000487525.5:c.*322_*323delinsGG ENSP00000431637.1:n.*322_*323delinsGG
ENST00000578151.1:n.84_85delinsGG
ENST00000581221.5:n.264_265delinsGG
ENST00000583539.5:c.749_750delinsGG ENSP00000463121.1:p.His250Arg
ENST00000584617.5:c.471_472delinsGG
ENST00000584804.1:c.44_45delinsGG ENSP00000463658.1:p.His15Arg
ENST00000697678.1:n.651_652delinsGG
ENST00000697679.1:n.1823_1824delinsGG
ENST00000697680.1:c.*1613_*1614delinsGG ENSP00000513392.1:n.*1613_*1614delinsGG
ENST00000697681.1:c.*1910_*1911delinsGG ENSP00000513393.1:n.*1910_*1911delinsGG
ENST00000697683.1:c.*1613_*1614delinsGG ENSP00000513395.1:n.*1613_*1614delinsGG
ENST00000697684.1:n.809_810delinsGG
ENST00000697685.1:c.*1446_*1447delinsGG ENSP00000513396.1:n.*1446_*1447delinsGG
ENST00000697686.1:c.398_399delinsGG ENSP00000513397.1:p.His133Arg
ENST00000697687.1:n.628_629delinsGG
ENST00000697688.1:n.795_796delinsGG
ENST00000697689.1:c.*1285_*1286delinsGG ENSP00000513398.1:n.*1285_*1286delinsGG
ENST00000697690.1:c.749_750delinsGG ENSP00000513399.1:p.His250Arg
ENST00000697691.1:c.*721_*722delinsGG ENSP00000513400.1:n.*721_*722delinsGG
ENST00000697692.1:c.*761_*762delinsGG ENSP00000513401.1:n.*761_*762delinsGG
ENST00000697694.1:c.398_399delinsGG ENSP00000513402.1:p.His133Arg
ENST00000697695.1:n.1356_1357delinsGG
XM_006722001.2:c.749_750delinsGG XP_006722064.1:p.His250Arg
XM_006722001.4:c.749_750delinsGG XP_006722064.1:p.His250Arg
XM_006722002.2:c.749_750delinsGG XP_006722065.1:p.His250Arg
XM_006722002.4:c.749_750delinsGG XP_006722065.1:p.His250Arg
XM_006722004.2:c.398_399delinsGG XP_006722067.1:p.His133Arg
XM_006722004.3:c.398_399delinsGG XP_006722067.1:p.His133Arg
XM_006722005.2:c.398_399delinsGG XP_006722068.1:p.His133Arg
XM_006722005.3:c.398_399delinsGG XP_006722068.1:p.His133Arg
XM_011525092.1:c.398_399delinsGG XP_011523394.1:p.His133Arg
XM_011525092.2:c.398_399delinsGG XP_011523394.1:p.His133Arg
XM_011525093.1:c.398_399delinsGG XP_011523395.1:p.His133Arg
XM_011525093.2:c.398_399delinsGG XP_011523395.1:p.His133Arg
XM_011525094.1:c.398_399delinsGG XP_011523396.1:p.His133Arg
XM_011525094.2:c.398_399delinsGG XP_011523396.1:p.His133Arg
XM_017024914.1:c.398_399delinsGG XP_016880403.1:p.His133Arg
XM_017024915.1:c.398_399delinsGG XP_016880404.1:p.His133Arg
XM_017024916.1:c.398_399delinsGG XP_016880405.1:p.His133Arg
XM_017024917.1:c.398_399delinsGG XP_016880406.1:p.His133Arg
XM_017024918.2:c.398_399delinsGG XP_016880407.1:p.His133Arg
XM_017024919.1:c.398_399delinsGG XP_016880408.1:p.His133Arg
XR_934513.1:n.967_968delinsGG
XR_934513.3:n.1398_1399delinsGG
XR_934514.1:n.967_968delinsGG
XR_934514.3:n.1398_1399delinsGG