Canonical Allele Identifier: CA3261179161
Community Standard Title: NM_058216.3(RAD51C):c.610_612delinsGTG (p.Ile204Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703234_58703236delinsGTG , CM000679.2:g.58703234_58703236delinsGTG GRCh38
NC_000017.10:g.56780595_56780597delinsGTG , CM000679.1:g.56780595_56780597delinsGTG GRCh37
NC_000017.9:g.54135594_54135596delinsGTG NCBI36
NG_023199.1:g.15633_15635delinsGTG , LRG_314:g.15633_15635delinsGTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.610_612delinsGTG MANE Select NP_478123.1:p.Ile204Val
ENST00000337432.9:c.610_612delinsGTG MANE Select ENSP00000336701.4:p.Ile204Val
NM_058216.2:c.610_612delinsGTG NP_478123.1:p.Ile204Val
NR_103872.1:n.514_516delinsGTG
NR_103872.2:n.485_487delinsGTG
ENST00000337432.8:c.610_612delinsGTG ENSP00000336701.4:p.Ile204Val
ENST00000413590.5:c.248_250delinsGTG
ENST00000425173.5:c.406_408delinsGTG ENSP00000407282.1:p.Ile136Val
ENST00000461271.5:c.259_261delinsGTG ENSP00000464056.1:p.Ile87Val
ENST00000461271.6:c.259_261delinsGTG ENSP00000464056.2:p.Ile87Val
ENST00000475762.5:c.*1313_*1315delinsGTG ENSP00000432421.1:n.*1313_*1315delinsGTG
ENST00000482007.5:c.*38_*40delinsGTG ENSP00000433332.1:n.*38_*40delinsGTG
ENST00000487525.5:c.*38_*40delinsGTG ENSP00000431637.1:n.*38_*40delinsGTG
ENST00000487921.5:n.522_524delinsGTG
ENST00000583539.5:c.610_612delinsGTG ENSP00000463121.1:p.Ile204Val
ENST00000584617.5:c.332_334delinsGTG
ENST00000697677.1:n.1691_1693delinsGTG
ENST00000697678.1:n.512_514delinsGTG
ENST00000697679.1:n.1684_1686delinsGTG
ENST00000697680.1:c.*1474_*1476delinsGTG ENSP00000513392.1:n.*1474_*1476delinsGTG
ENST00000697681.1:c.*1626_*1628delinsGTG ENSP00000513393.1:n.*1626_*1628delinsGTG
ENST00000697683.1:c.*1474_*1476delinsGTG ENSP00000513395.1:n.*1474_*1476delinsGTG
ENST00000697684.1:n.670_672delinsGTG
ENST00000697685.1:c.*1307_*1309delinsGTG ENSP00000513396.1:n.*1307_*1309delinsGTG
ENST00000697686.1:c.259_261delinsGTG ENSP00000513397.1:p.Ile87Val
ENST00000697687.1:n.489_491delinsGTG
ENST00000697688.1:n.656_658delinsGTG
ENST00000697689.1:c.*1146_*1148delinsGTG ENSP00000513398.1:n.*1146_*1148delinsGTG
ENST00000697690.1:c.610_612delinsGTG ENSP00000513399.1:p.Ile204Val
ENST00000697691.1:c.*582_*584delinsGTG ENSP00000513400.1:n.*582_*584delinsGTG
ENST00000697692.1:c.*622_*624delinsGTG ENSP00000513401.1:n.*622_*624delinsGTG
ENST00000697694.1:c.259_261delinsGTG ENSP00000513402.1:p.Ile87Val
ENST00000697695.1:n.1217_1219delinsGTG
XM_006722001.2:c.610_612delinsGTG XP_006722064.1:p.Ile204Val
XM_006722001.4:c.610_612delinsGTG XP_006722064.1:p.Ile204Val
XM_006722002.2:c.610_612delinsGTG XP_006722065.1:p.Ile204Val
XM_006722002.4:c.610_612delinsGTG XP_006722065.1:p.Ile204Val
XM_006722004.2:c.259_261delinsGTG XP_006722067.1:p.Ile87Val
XM_006722004.3:c.259_261delinsGTG XP_006722067.1:p.Ile87Val
XM_006722005.2:c.259_261delinsGTG XP_006722068.1:p.Ile87Val
XM_006722005.3:c.259_261delinsGTG XP_006722068.1:p.Ile87Val
XM_011525092.1:c.259_261delinsGTG XP_011523394.1:p.Ile87Val
XM_011525092.2:c.259_261delinsGTG XP_011523394.1:p.Ile87Val
XM_011525093.1:c.259_261delinsGTG XP_011523395.1:p.Ile87Val
XM_011525093.2:c.259_261delinsGTG XP_011523395.1:p.Ile87Val
XM_011525094.1:c.259_261delinsGTG XP_011523396.1:p.Ile87Val
XM_011525094.2:c.259_261delinsGTG XP_011523396.1:p.Ile87Val
XM_017024914.1:c.259_261delinsGTG XP_016880403.1:p.Ile87Val
XM_017024915.1:c.259_261delinsGTG XP_016880404.1:p.Ile87Val
XM_017024916.1:c.259_261delinsGTG XP_016880405.1:p.Ile87Val
XM_017024917.1:c.259_261delinsGTG XP_016880406.1:p.Ile87Val
XM_017024918.2:c.259_261delinsGTG XP_016880407.1:p.Ile87Val
XM_017024919.1:c.259_261delinsGTG XP_016880408.1:p.Ile87Val
XR_934513.1:n.683_685delinsGTG
XR_934513.3:n.1114_1116delinsGTG
XR_934514.1:n.683_685delinsGTG
XR_934514.3:n.1114_1116delinsGTG