Canonical Allele Identifier: CA3261179458
Community Standard Title: NM_058216.3(RAD51C):c.340_342delinsCGG (p.Gly114Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695125_58695127delinsCGG , CM000679.2:g.58695125_58695127delinsCGG GRCh38
NC_000017.10:g.56772486_56772488delinsCGG , CM000679.1:g.56772486_56772488delinsCGG GRCh37
NC_000017.9:g.54127485_54127487delinsCGG NCBI36
NG_023199.1:g.7524_7526delinsCGG , LRG_314:g.7524_7526delinsCGG
NG_047169.1:g.1953_1955delinsCCG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.340_342delinsCGG MANE Select NP_478123.1:p.Gly114Arg
ENST00000337432.9:c.340_342delinsCGG MANE Select ENSP00000336701.4:p.Gly114Arg
NM_002876.3:c.340_342delinsCGG NP_002867.1:p.Gly114Arg
NM_002876.4:c.340_342delinsCGG NP_002867.1:p.Gly114Arg
NM_058216.2:c.340_342delinsCGG NP_478123.1:p.Gly114Arg
NR_103872.1:n.411_413delinsCGG
NR_103872.2:n.382_384delinsCGG
NR_103873.1:n.308_310delinsCGG
ENST00000337432.8:c.340_342delinsCGG ENSP00000336701.4:p.Gly114Arg
ENST00000421782.3:c.340_342delinsCGG ENSP00000391450.2:p.Gly114Arg
ENST00000425173.5:c.136_138delinsCGG ENSP00000407282.1:p.Gly46Arg
ENST00000461271.5:c.-12_-10delinsCGG ENSP00000464056.1:n.-12_-10delinsCGG
ENST00000461271.6:c.-12_-10delinsCGG ENSP00000464056.2:n.-12_-10delinsCGG
ENST00000475762.5:c.*1043_*1045delinsCGG ENSP00000432421.1:n.*1043_*1045delinsCGG
ENST00000482007.5:c.340_342delinsCGG ENSP00000433332.1:p.Gly114Arg
ENST00000486827.1:c.*1204_*1206delinsCGG ENSP00000436761.1:n.*1204_*1206delinsCGG
ENST00000487525.5:c.340_342delinsCGG ENSP00000431637.1:p.Gly114Arg
ENST00000487921.5:n.252_254delinsCGG
ENST00000583539.5:c.340_342delinsCGG ENSP00000463121.1:p.Gly114Arg
ENST00000584617.5:c.127-1568_127-1566delinsCGG
ENST00000622327.4:c.76_78delinsCGG ENSP00000482326.1:p.Gly26Arg
ENST00000697675.1:n.1434_1436delinsCGG
ENST00000697676.1:n.400_402delinsCGG
ENST00000697677.1:n.1421_1423delinsCGG
ENST00000697678.1:n.242_244delinsCGG
ENST00000697679.1:n.1414_1416delinsCGG
ENST00000697680.1:c.*1204_*1206delinsCGG ENSP00000513392.1:n.*1204_*1206delinsCGG
ENST00000697681.1:c.*1204_*1206delinsCGG ENSP00000513393.1:n.*1204_*1206delinsCGG
ENST00000697683.1:c.*1204_*1206delinsCGG ENSP00000513395.1:n.*1204_*1206delinsCGG
ENST00000697684.1:n.400_402delinsCGG
ENST00000697685.1:c.*1204_*1206delinsCGG ENSP00000513396.1:n.*1204_*1206delinsCGG
ENST00000697686.1:c.-12_-10delinsCGG ENSP00000513397.1:n.-12_-10delinsCGG
ENST00000697687.1:n.386_388delinsCGG
ENST00000697688.1:n.386_388delinsCGG
ENST00000697689.1:c.*1043_*1045delinsCGG ENSP00000513398.1:n.*1043_*1045delinsCGG
ENST00000697690.1:c.340_342delinsCGG ENSP00000513399.1:p.Gly114Arg
ENST00000697691.1:c.*312_*314delinsCGG ENSP00000513400.1:n.*312_*314delinsCGG
ENST00000697692.1:c.*352_*354delinsCGG ENSP00000513401.1:n.*352_*354delinsCGG
ENST00000697693.1:n.1115_1117delinsCGG
ENST00000697694.1:c.-12_-10delinsCGG ENSP00000513402.1:n.-12_-10delinsCGG
ENST00000697695.1:n.947_949delinsCGG
XM_006722001.2:c.340_342delinsCGG XP_006722064.1:p.Gly114Arg
XM_006722001.4:c.340_342delinsCGG XP_006722064.1:p.Gly114Arg
XM_006722002.2:c.340_342delinsCGG XP_006722065.1:p.Gly114Arg
XM_006722002.4:c.340_342delinsCGG XP_006722065.1:p.Gly114Arg
XM_006722004.2:c.-12_-10delinsCGG XP_006722067.1:n.-12_-10delinsCGG
XM_006722004.3:c.-12_-10delinsCGG XP_006722067.1:n.-12_-10delinsCGG
XM_006722005.2:c.-12_-10delinsCGG XP_006722068.1:n.-12_-10delinsCGG
XM_006722005.3:c.-12_-10delinsCGG XP_006722068.1:n.-12_-10delinsCGG
XM_011525092.1:c.-12_-10delinsCGG XP_011523394.1:n.-12_-10delinsCGG
XM_011525092.2:c.-12_-10delinsCGG XP_011523394.1:n.-12_-10delinsCGG
XM_011525093.1:c.-12_-10delinsCGG XP_011523395.1:n.-12_-10delinsCGG
XM_011525093.2:c.-12_-10delinsCGG XP_011523395.1:n.-12_-10delinsCGG
XM_011525094.1:c.-12_-10delinsCGG XP_011523396.1:n.-12_-10delinsCGG
XM_011525094.2:c.-12_-10delinsCGG XP_011523396.1:n.-12_-10delinsCGG
XM_017024914.1:c.-12_-10delinsCGG XP_016880403.1:n.-12_-10delinsCGG
XM_017024915.1:c.-12_-10delinsCGG XP_016880404.1:n.-12_-10delinsCGG
XM_017024916.1:c.-12_-10delinsCGG XP_016880405.1:n.-12_-10delinsCGG
XM_017024917.1:c.-12_-10delinsCGG XP_016880406.1:n.-12_-10delinsCGG
XM_017024918.2:c.-12_-10delinsCGG XP_016880407.1:n.-12_-10delinsCGG
XM_017024919.1:c.-12_-10delinsCGG XP_016880408.1:n.-12_-10delinsCGG
XR_934513.1:n.413_415delinsCGG
XR_934513.3:n.844_846delinsCGG
XR_934514.1:n.413_415delinsCGG
XR_934514.3:n.844_846delinsCGG