Canonical Allele Identifier: CA3261178812
Community Standard Title: NM_058216.3(RAD51C):c.301_303delinsGTG (p.Ile101Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695086_58695088delinsGTG , CM000679.2:g.58695086_58695088delinsGTG GRCh38
NC_000017.10:g.56772447_56772449delinsGTG , CM000679.1:g.56772447_56772449delinsGTG GRCh37
NC_000017.9:g.54127446_54127448delinsGTG NCBI36
NG_023199.1:g.7485_7487delinsGTG , LRG_314:g.7485_7487delinsGTG
NG_047169.1:g.1992_1994delinsCAC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.301_303delinsGTG MANE Select NP_478123.1:p.Ile101Val
ENST00000337432.9:c.301_303delinsGTG MANE Select ENSP00000336701.4:p.Ile101Val
NM_002876.3:c.301_303delinsGTG NP_002867.1:p.Ile101Val
NM_002876.4:c.301_303delinsGTG NP_002867.1:p.Ile101Val
NM_058216.2:c.301_303delinsGTG NP_478123.1:p.Ile101Val
NR_103872.1:n.372_374delinsGTG
NR_103872.2:n.343_345delinsGTG
NR_103873.1:n.269_271delinsGTG
ENST00000337432.8:c.301_303delinsGTG ENSP00000336701.4:p.Ile101Val
ENST00000421782.3:c.301_303delinsGTG ENSP00000391450.2:p.Ile101Val
ENST00000425173.5:c.97_99delinsGTG ENSP00000407282.1:p.Ile33Val
ENST00000461271.5:c.-51_-49delinsGTG ENSP00000464056.1:n.-51_-49delinsGTG
ENST00000461271.6:c.-51_-49delinsGTG ENSP00000464056.2:n.-51_-49delinsGTG
ENST00000475762.5:c.*1004_*1006delinsGTG ENSP00000432421.1:n.*1004_*1006delinsGTG
ENST00000482007.5:c.301_303delinsGTG ENSP00000433332.1:p.Ile101Val
ENST00000486827.1:c.*1165_*1167delinsGTG ENSP00000436761.1:n.*1165_*1167delinsGTG
ENST00000487525.5:c.301_303delinsGTG ENSP00000431637.1:p.Ile101Val
ENST00000487921.5:n.213_215delinsGTG
ENST00000583539.5:c.301_303delinsGTG ENSP00000463121.1:p.Ile101Val
ENST00000584617.5:c.127-1607_127-1605delinsGTG
ENST00000622327.4:c.37_39delinsGTG ENSP00000482326.1:p.Ile13Val
ENST00000697675.1:n.1395_1397delinsGTG
ENST00000697676.1:n.361_363delinsGTG
ENST00000697677.1:n.1382_1384delinsGTG
ENST00000697678.1:n.203_205delinsGTG
ENST00000697679.1:n.1375_1377delinsGTG
ENST00000697680.1:c.*1165_*1167delinsGTG ENSP00000513392.1:n.*1165_*1167delinsGTG
ENST00000697681.1:c.*1165_*1167delinsGTG ENSP00000513393.1:n.*1165_*1167delinsGTG
ENST00000697683.1:c.*1165_*1167delinsGTG ENSP00000513395.1:n.*1165_*1167delinsGTG
ENST00000697684.1:n.361_363delinsGTG
ENST00000697685.1:c.*1165_*1167delinsGTG ENSP00000513396.1:n.*1165_*1167delinsGTG
ENST00000697686.1:c.-51_-49delinsGTG ENSP00000513397.1:n.-51_-49delinsGTG
ENST00000697687.1:n.347_349delinsGTG
ENST00000697688.1:n.347_349delinsGTG
ENST00000697689.1:c.*1004_*1006delinsGTG ENSP00000513398.1:n.*1004_*1006delinsGTG
ENST00000697690.1:c.301_303delinsGTG ENSP00000513399.1:p.Ile101Val
ENST00000697691.1:c.*273_*275delinsGTG ENSP00000513400.1:n.*273_*275delinsGTG
ENST00000697692.1:c.*313_*315delinsGTG ENSP00000513401.1:n.*313_*315delinsGTG
ENST00000697693.1:n.1076_1078delinsGTG
ENST00000697694.1:c.-51_-49delinsGTG ENSP00000513402.1:n.-51_-49delinsGTG
ENST00000697695.1:n.908_910delinsGTG
XM_006722001.2:c.301_303delinsGTG XP_006722064.1:p.Ile101Val
XM_006722001.4:c.301_303delinsGTG XP_006722064.1:p.Ile101Val
XM_006722002.2:c.301_303delinsGTG XP_006722065.1:p.Ile101Val
XM_006722002.4:c.301_303delinsGTG XP_006722065.1:p.Ile101Val
XM_006722004.2:c.-51_-49delinsGTG XP_006722067.1:n.-51_-49delinsGTG
XM_006722004.3:c.-51_-49delinsGTG XP_006722067.1:n.-51_-49delinsGTG
XM_006722005.2:c.-51_-49delinsGTG XP_006722068.1:n.-51_-49delinsGTG
XM_006722005.3:c.-51_-49delinsGTG XP_006722068.1:n.-51_-49delinsGTG
XM_011525092.1:c.-51_-49delinsGTG XP_011523394.1:n.-51_-49delinsGTG
XM_011525092.2:c.-51_-49delinsGTG XP_011523394.1:n.-51_-49delinsGTG
XM_011525093.1:c.-51_-49delinsGTG XP_011523395.1:n.-51_-49delinsGTG
XM_011525093.2:c.-51_-49delinsGTG XP_011523395.1:n.-51_-49delinsGTG
XM_011525094.1:c.-51_-49delinsGTG XP_011523396.1:n.-51_-49delinsGTG
XM_011525094.2:c.-51_-49delinsGTG XP_011523396.1:n.-51_-49delinsGTG
XM_017024914.1:c.-51_-49delinsGTG XP_016880403.1:n.-51_-49delinsGTG
XM_017024915.1:c.-51_-49delinsGTG XP_016880404.1:n.-51_-49delinsGTG
XM_017024916.1:c.-51_-49delinsGTG XP_016880405.1:n.-51_-49delinsGTG
XM_017024917.1:c.-51_-49delinsGTG XP_016880406.1:n.-51_-49delinsGTG
XM_017024918.2:c.-51_-49delinsGTG XP_016880407.1:n.-51_-49delinsGTG
XM_017024919.1:c.-51_-49delinsGTG XP_016880408.1:n.-51_-49delinsGTG
XR_934513.1:n.374_376delinsGTG
XR_934513.3:n.805_807delinsGTG
XR_934514.1:n.374_376delinsGTG
XR_934514.3:n.805_807delinsGTG