Canonical Allele Identifier: CA3261180137
Community Standard Title: NM_058216.3(RAD51C):c.803_804delinsGG (p.Gln268Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709956_58709957delinsGG , CM000679.2:g.58709956_58709957delinsGG GRCh38
NC_000017.10:g.56787317_56787318delinsGG , CM000679.1:g.56787317_56787318delinsGG GRCh37
NC_000017.9:g.54142316_54142317delinsGG NCBI36
NG_023199.1:g.22355_22356delinsGG , LRG_314:g.22355_22356delinsGG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.803_804delinsGG MANE Select NP_478123.1:p.Gln268Arg
ENST00000337432.9:c.803_804delinsGG MANE Select ENSP00000336701.4:p.Gln268Arg
NM_058216.2:c.803_804delinsGG NP_478123.1:p.Gln268Arg
NR_103872.1:n.707_708delinsGG
NR_103872.2:n.678_679delinsGG
ENST00000337432.8:c.803_804delinsGG ENSP00000336701.4:p.Gln268Arg
ENST00000413590.5:c.441_442delinsGG
ENST00000461271.6:c.452_453delinsGG ENSP00000464056.2:p.Gln151Arg
ENST00000475762.5:c.*1506_*1507delinsGG ENSP00000432421.1:n.*1506_*1507delinsGG
ENST00000482007.5:c.*231_*232delinsGG ENSP00000433332.1:n.*231_*232delinsGG
ENST00000487525.5:c.*376_*377delinsGG ENSP00000431637.1:n.*376_*377delinsGG
ENST00000578151.1:n.138_139delinsGG
ENST00000581221.5:n.318_319delinsGG
ENST00000583539.5:c.803_804delinsGG ENSP00000463121.1:p.Gln268Arg
ENST00000584617.5:c.525_526delinsGG
ENST00000584804.1:c.98_99delinsGG ENSP00000463658.1:p.Gln33Arg
ENST00000697678.1:n.705_706delinsGG
ENST00000697679.1:n.1877_1878delinsGG
ENST00000697680.1:c.*1667_*1668delinsGG ENSP00000513392.1:n.*1667_*1668delinsGG
ENST00000697681.1:c.*1964_*1965delinsGG ENSP00000513393.1:n.*1964_*1965delinsGG
ENST00000697683.1:c.*1667_*1668delinsGG ENSP00000513395.1:n.*1667_*1668delinsGG
ENST00000697684.1:n.863_864delinsGG
ENST00000697685.1:c.*1500_*1501delinsGG ENSP00000513396.1:n.*1500_*1501delinsGG
ENST00000697686.1:c.452_453delinsGG ENSP00000513397.1:p.Gln151Arg
ENST00000697687.1:n.682_683delinsGG
ENST00000697688.1:n.849_850delinsGG
ENST00000697689.1:c.*1339_*1340delinsGG ENSP00000513398.1:n.*1339_*1340delinsGG
ENST00000697690.1:c.803_804delinsGG ENSP00000513399.1:p.Gln268Arg
ENST00000697691.1:c.*775_*776delinsGG ENSP00000513400.1:n.*775_*776delinsGG
ENST00000697692.1:c.*815_*816delinsGG ENSP00000513401.1:n.*815_*816delinsGG
ENST00000697694.1:c.452_453delinsGG ENSP00000513402.1:p.Gln151Arg
ENST00000697695.1:n.1410_1411delinsGG
XM_006722001.2:c.803_804delinsGG XP_006722064.1:p.Gln268Arg
XM_006722001.4:c.803_804delinsGG XP_006722064.1:p.Gln268Arg
XM_006722002.2:c.803_804delinsGG XP_006722065.1:p.Gln268Arg
XM_006722002.4:c.803_804delinsGG XP_006722065.1:p.Gln268Arg
XM_006722004.2:c.452_453delinsGG XP_006722067.1:p.Gln151Arg
XM_006722004.3:c.452_453delinsGG XP_006722067.1:p.Gln151Arg
XM_006722005.2:c.452_453delinsGG XP_006722068.1:p.Gln151Arg
XM_006722005.3:c.452_453delinsGG XP_006722068.1:p.Gln151Arg
XM_011525092.1:c.452_453delinsGG XP_011523394.1:p.Gln151Arg
XM_011525092.2:c.452_453delinsGG XP_011523394.1:p.Gln151Arg
XM_011525093.1:c.452_453delinsGG XP_011523395.1:p.Gln151Arg
XM_011525093.2:c.452_453delinsGG XP_011523395.1:p.Gln151Arg
XM_011525094.1:c.452_453delinsGG XP_011523396.1:p.Gln151Arg
XM_011525094.2:c.452_453delinsGG XP_011523396.1:p.Gln151Arg
XM_017024914.1:c.452_453delinsGG XP_016880403.1:p.Gln151Arg
XM_017024915.1:c.452_453delinsGG XP_016880404.1:p.Gln151Arg
XM_017024916.1:c.452_453delinsGG XP_016880405.1:p.Gln151Arg
XM_017024917.1:c.452_453delinsGG XP_016880406.1:p.Gln151Arg
XM_017024918.2:c.452_453delinsGG XP_016880407.1:p.Gln151Arg
XM_017024919.1:c.452_453delinsGG XP_016880408.1:p.Gln151Arg
XR_934513.1:n.1021_1022delinsGG
XR_934513.3:n.1452_1453delinsGG
XR_934514.1:n.1021_1022delinsGG
XR_934514.3:n.1452_1453delinsGG