Canonical Allele Identifier: CA3261179312
Community Standard Title: NM_058216.3(RAD51C):c.622_624delinsGTG (p.Ile208Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703246_58703248delinsGTG , CM000679.2:g.58703246_58703248delinsGTG GRCh38
NC_000017.10:g.56780607_56780609delinsGTG , CM000679.1:g.56780607_56780609delinsGTG GRCh37
NC_000017.9:g.54135606_54135608delinsGTG NCBI36
NG_023199.1:g.15645_15647delinsGTG , LRG_314:g.15645_15647delinsGTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.622_624delinsGTG MANE Select NP_478123.1:p.Ile208Val
ENST00000337432.9:c.622_624delinsGTG MANE Select ENSP00000336701.4:p.Ile208Val
NM_058216.2:c.622_624delinsGTG NP_478123.1:p.Ile208Val
NR_103872.1:n.526_528delinsGTG
NR_103872.2:n.497_499delinsGTG
ENST00000337432.8:c.622_624delinsGTG ENSP00000336701.4:p.Ile208Val
ENST00000413590.5:c.260_262delinsGTG
ENST00000425173.5:c.418_420delinsGTG ENSP00000407282.1:p.Ile140Val
ENST00000461271.5:c.271_273delinsGTG ENSP00000464056.1:p.Ile91Val
ENST00000461271.6:c.271_273delinsGTG ENSP00000464056.2:p.Ile91Val
ENST00000475762.5:c.*1325_*1327delinsGTG ENSP00000432421.1:n.*1325_*1327delinsGTG
ENST00000482007.5:c.*50_*52delinsGTG ENSP00000433332.1:n.*50_*52delinsGTG
ENST00000487525.5:c.*50_*52delinsGTG ENSP00000431637.1:n.*50_*52delinsGTG
ENST00000487921.5:n.534_536delinsGTG
ENST00000583539.5:c.622_624delinsGTG ENSP00000463121.1:p.Ile208Val
ENST00000584617.5:c.344_346delinsGTG
ENST00000697677.1:n.1703_1705delinsGTG
ENST00000697678.1:n.524_526delinsGTG
ENST00000697679.1:n.1696_1698delinsGTG
ENST00000697680.1:c.*1486_*1488delinsGTG ENSP00000513392.1:n.*1486_*1488delinsGTG
ENST00000697681.1:c.*1638_*1640delinsGTG ENSP00000513393.1:n.*1638_*1640delinsGTG
ENST00000697683.1:c.*1486_*1488delinsGTG ENSP00000513395.1:n.*1486_*1488delinsGTG
ENST00000697684.1:n.682_684delinsGTG
ENST00000697685.1:c.*1319_*1321delinsGTG ENSP00000513396.1:n.*1319_*1321delinsGTG
ENST00000697686.1:c.271_273delinsGTG ENSP00000513397.1:p.Ile91Val
ENST00000697687.1:n.501_503delinsGTG
ENST00000697688.1:n.668_670delinsGTG
ENST00000697689.1:c.*1158_*1160delinsGTG ENSP00000513398.1:n.*1158_*1160delinsGTG
ENST00000697690.1:c.622_624delinsGTG ENSP00000513399.1:p.Ile208Val
ENST00000697691.1:c.*594_*596delinsGTG ENSP00000513400.1:n.*594_*596delinsGTG
ENST00000697692.1:c.*634_*636delinsGTG ENSP00000513401.1:n.*634_*636delinsGTG
ENST00000697694.1:c.271_273delinsGTG ENSP00000513402.1:p.Ile91Val
ENST00000697695.1:n.1229_1231delinsGTG
XM_006722001.2:c.622_624delinsGTG XP_006722064.1:p.Ile208Val
XM_006722001.4:c.622_624delinsGTG XP_006722064.1:p.Ile208Val
XM_006722002.2:c.622_624delinsGTG XP_006722065.1:p.Ile208Val
XM_006722002.4:c.622_624delinsGTG XP_006722065.1:p.Ile208Val
XM_006722004.2:c.271_273delinsGTG XP_006722067.1:p.Ile91Val
XM_006722004.3:c.271_273delinsGTG XP_006722067.1:p.Ile91Val
XM_006722005.2:c.271_273delinsGTG XP_006722068.1:p.Ile91Val
XM_006722005.3:c.271_273delinsGTG XP_006722068.1:p.Ile91Val
XM_011525092.1:c.271_273delinsGTG XP_011523394.1:p.Ile91Val
XM_011525092.2:c.271_273delinsGTG XP_011523394.1:p.Ile91Val
XM_011525093.1:c.271_273delinsGTG XP_011523395.1:p.Ile91Val
XM_011525093.2:c.271_273delinsGTG XP_011523395.1:p.Ile91Val
XM_011525094.1:c.271_273delinsGTG XP_011523396.1:p.Ile91Val
XM_011525094.2:c.271_273delinsGTG XP_011523396.1:p.Ile91Val
XM_017024914.1:c.271_273delinsGTG XP_016880403.1:p.Ile91Val
XM_017024915.1:c.271_273delinsGTG XP_016880404.1:p.Ile91Val
XM_017024916.1:c.271_273delinsGTG XP_016880405.1:p.Ile91Val
XM_017024917.1:c.271_273delinsGTG XP_016880406.1:p.Ile91Val
XM_017024918.2:c.271_273delinsGTG XP_016880407.1:p.Ile91Val
XM_017024919.1:c.271_273delinsGTG XP_016880408.1:p.Ile91Val
XR_934513.1:n.695_697delinsGTG
XR_934513.3:n.1126_1128delinsGTG
XR_934514.1:n.695_697delinsGTG
XR_934514.3:n.1126_1128delinsGTG