Canonical Allele Identifier: CA3261179564
Community Standard Title: NM_058216.3(RAD51C):c.347_348delinsGG (p.Pro116Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695132_58695133delinsGG , CM000679.2:g.58695132_58695133delinsGG GRCh38
NC_000017.10:g.56772493_56772494delinsGG , CM000679.1:g.56772493_56772494delinsGG GRCh37
NC_000017.9:g.54127492_54127493delinsGG NCBI36
NG_023199.1:g.7531_7532delinsGG , LRG_314:g.7531_7532delinsGG
NG_047169.1:g.1947_1948delinsCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.347_348delinsGG MANE Select NP_478123.1:p.Pro116Arg
ENST00000337432.9:c.347_348delinsGG MANE Select ENSP00000336701.4:p.Pro116Arg
NM_002876.3:c.347_348delinsGG NP_002867.1:p.Pro116Arg
NM_002876.4:c.347_348delinsGG NP_002867.1:p.Pro116Arg
NM_058216.2:c.347_348delinsGG NP_478123.1:p.Pro116Arg
NR_103872.1:n.418_419delinsGG
NR_103872.2:n.389_390delinsGG
NR_103873.1:n.315_316delinsGG
ENST00000337432.8:c.347_348delinsGG ENSP00000336701.4:p.Pro116Arg
ENST00000421782.3:c.347_348delinsGG ENSP00000391450.2:p.Pro116Arg
ENST00000425173.5:c.143_144delinsGG ENSP00000407282.1:p.Pro48Arg
ENST00000461271.5:c.-5_-4delinsGG ENSP00000464056.1:n.-5_-4delinsGG
ENST00000461271.6:c.-5_-4delinsGG ENSP00000464056.2:n.-5_-4delinsGG
ENST00000475762.5:c.*1050_*1051delinsGG ENSP00000432421.1:n.*1050_*1051delinsGG
ENST00000482007.5:c.347_348delinsGG ENSP00000433332.1:p.Pro116Arg
ENST00000486827.1:c.*1211_*1212delinsGG ENSP00000436761.1:n.*1211_*1212delinsGG
ENST00000487525.5:c.347_348delinsGG ENSP00000431637.1:p.Pro116Arg
ENST00000487921.5:n.259_260delinsGG
ENST00000583539.5:c.347_348delinsGG ENSP00000463121.1:p.Pro116Arg
ENST00000584617.5:c.127-1561_127-1560delinsGG
ENST00000622327.4:c.83_84delinsGG ENSP00000482326.1:p.Pro28Arg
ENST00000697675.1:n.1441_1442delinsGG
ENST00000697676.1:n.407_408delinsGG
ENST00000697677.1:n.1428_1429delinsGG
ENST00000697678.1:n.249_250delinsGG
ENST00000697679.1:n.1421_1422delinsGG
ENST00000697680.1:c.*1211_*1212delinsGG ENSP00000513392.1:n.*1211_*1212delinsGG
ENST00000697681.1:c.*1211_*1212delinsGG ENSP00000513393.1:n.*1211_*1212delinsGG
ENST00000697683.1:c.*1211_*1212delinsGG ENSP00000513395.1:n.*1211_*1212delinsGG
ENST00000697684.1:n.407_408delinsGG
ENST00000697685.1:c.*1211_*1212delinsGG ENSP00000513396.1:n.*1211_*1212delinsGG
ENST00000697686.1:c.-5_-4delinsGG ENSP00000513397.1:n.-5_-4delinsGG
ENST00000697687.1:n.393_394delinsGG
ENST00000697688.1:n.393_394delinsGG
ENST00000697689.1:c.*1050_*1051delinsGG ENSP00000513398.1:n.*1050_*1051delinsGG
ENST00000697690.1:c.347_348delinsGG ENSP00000513399.1:p.Pro116Arg
ENST00000697691.1:c.*319_*320delinsGG ENSP00000513400.1:n.*319_*320delinsGG
ENST00000697692.1:c.*359_*360delinsGG ENSP00000513401.1:n.*359_*360delinsGG
ENST00000697693.1:n.1122_1123delinsGG
ENST00000697694.1:c.-5_-4delinsGG ENSP00000513402.1:n.-5_-4delinsGG
ENST00000697695.1:n.954_955delinsGG
XM_006722001.2:c.347_348delinsGG XP_006722064.1:p.Pro116Arg
XM_006722001.4:c.347_348delinsGG XP_006722064.1:p.Pro116Arg
XM_006722002.2:c.347_348delinsGG XP_006722065.1:p.Pro116Arg
XM_006722002.4:c.347_348delinsGG XP_006722065.1:p.Pro116Arg
XM_006722004.2:c.-5_-4delinsGG XP_006722067.1:n.-5_-4delinsGG
XM_006722004.3:c.-5_-4delinsGG XP_006722067.1:n.-5_-4delinsGG
XM_006722005.2:c.-5_-4delinsGG XP_006722068.1:n.-5_-4delinsGG
XM_006722005.3:c.-5_-4delinsGG XP_006722068.1:n.-5_-4delinsGG
XM_011525092.1:c.-5_-4delinsGG XP_011523394.1:n.-5_-4delinsGG
XM_011525092.2:c.-5_-4delinsGG XP_011523394.1:n.-5_-4delinsGG
XM_011525093.1:c.-5_-4delinsGG XP_011523395.1:n.-5_-4delinsGG
XM_011525093.2:c.-5_-4delinsGG XP_011523395.1:n.-5_-4delinsGG
XM_011525094.1:c.-5_-4delinsGG XP_011523396.1:n.-5_-4delinsGG
XM_011525094.2:c.-5_-4delinsGG XP_011523396.1:n.-5_-4delinsGG
XM_017024914.1:c.-5_-4delinsGG XP_016880403.1:n.-5_-4delinsGG
XM_017024915.1:c.-5_-4delinsGG XP_016880404.1:n.-5_-4delinsGG
XM_017024916.1:c.-5_-4delinsGG XP_016880405.1:n.-5_-4delinsGG
XM_017024917.1:c.-5_-4delinsGG XP_016880406.1:n.-5_-4delinsGG
XM_017024918.2:c.-5_-4delinsGG XP_016880407.1:n.-5_-4delinsGG
XM_017024919.1:c.-5_-4delinsGG XP_016880408.1:n.-5_-4delinsGG
XR_934513.1:n.420_421delinsGG
XR_934513.3:n.851_852delinsGG
XR_934514.1:n.420_421delinsGG
XR_934514.3:n.851_852delinsGG