Canonical Allele Identifier: CA3261180124
Community Standard Title: NM_058216.3(RAD51C):c.802_804delinsAAG (p.Gln268Lys)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709955_58709957delinsAAG , CM000679.2:g.58709955_58709957delinsAAG GRCh38
NC_000017.10:g.56787316_56787318delinsAAG , CM000679.1:g.56787316_56787318delinsAAG GRCh37
NC_000017.9:g.54142315_54142317delinsAAG NCBI36
NG_023199.1:g.22354_22356delinsAAG , LRG_314:g.22354_22356delinsAAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.802_804delinsAAG MANE Select NP_478123.1:p.Gln268Lys
ENST00000337432.9:c.802_804delinsAAG MANE Select ENSP00000336701.4:p.Gln268Lys
NM_058216.2:c.802_804delinsAAG NP_478123.1:p.Gln268Lys
NR_103872.1:n.706_708delinsAAG
NR_103872.2:n.677_679delinsAAG
ENST00000337432.8:c.802_804delinsAAG ENSP00000336701.4:p.Gln268Lys
ENST00000413590.5:c.440_442delinsAAG
ENST00000461271.6:c.451_453delinsAAG ENSP00000464056.2:p.Gln151Lys
ENST00000475762.5:c.*1505_*1507delinsAAG ENSP00000432421.1:n.*1505_*1507delinsAAG
ENST00000482007.5:c.*230_*232delinsAAG ENSP00000433332.1:n.*230_*232delinsAAG
ENST00000487525.5:c.*375_*377delinsAAG ENSP00000431637.1:n.*375_*377delinsAAG
ENST00000578151.1:n.137_139delinsAAG
ENST00000581221.5:n.317_319delinsAAG
ENST00000583539.5:c.802_804delinsAAG ENSP00000463121.1:p.Gln268Lys
ENST00000584617.5:c.524_526delinsAAG
ENST00000584804.1:c.97_99delinsAAG ENSP00000463658.1:p.Gln33Lys
ENST00000697678.1:n.704_706delinsAAG
ENST00000697679.1:n.1876_1878delinsAAG
ENST00000697680.1:c.*1666_*1668delinsAAG ENSP00000513392.1:n.*1666_*1668delinsAAG
ENST00000697681.1:c.*1963_*1965delinsAAG ENSP00000513393.1:n.*1963_*1965delinsAAG
ENST00000697683.1:c.*1666_*1668delinsAAG ENSP00000513395.1:n.*1666_*1668delinsAAG
ENST00000697684.1:n.862_864delinsAAG
ENST00000697685.1:c.*1499_*1501delinsAAG ENSP00000513396.1:n.*1499_*1501delinsAAG
ENST00000697686.1:c.451_453delinsAAG ENSP00000513397.1:p.Gln151Lys
ENST00000697687.1:n.681_683delinsAAG
ENST00000697688.1:n.848_850delinsAAG
ENST00000697689.1:c.*1338_*1340delinsAAG ENSP00000513398.1:n.*1338_*1340delinsAAG
ENST00000697690.1:c.802_804delinsAAG ENSP00000513399.1:p.Gln268Lys
ENST00000697691.1:c.*774_*776delinsAAG ENSP00000513400.1:n.*774_*776delinsAAG
ENST00000697692.1:c.*814_*816delinsAAG ENSP00000513401.1:n.*814_*816delinsAAG
ENST00000697694.1:c.451_453delinsAAG ENSP00000513402.1:p.Gln151Lys
ENST00000697695.1:n.1409_1411delinsAAG
XM_006722001.2:c.802_804delinsAAG XP_006722064.1:p.Gln268Lys
XM_006722001.4:c.802_804delinsAAG XP_006722064.1:p.Gln268Lys
XM_006722002.2:c.802_804delinsAAG XP_006722065.1:p.Gln268Lys
XM_006722002.4:c.802_804delinsAAG XP_006722065.1:p.Gln268Lys
XM_006722004.2:c.451_453delinsAAG XP_006722067.1:p.Gln151Lys
XM_006722004.3:c.451_453delinsAAG XP_006722067.1:p.Gln151Lys
XM_006722005.2:c.451_453delinsAAG XP_006722068.1:p.Gln151Lys
XM_006722005.3:c.451_453delinsAAG XP_006722068.1:p.Gln151Lys
XM_011525092.1:c.451_453delinsAAG XP_011523394.1:p.Gln151Lys
XM_011525092.2:c.451_453delinsAAG XP_011523394.1:p.Gln151Lys
XM_011525093.1:c.451_453delinsAAG XP_011523395.1:p.Gln151Lys
XM_011525093.2:c.451_453delinsAAG XP_011523395.1:p.Gln151Lys
XM_011525094.1:c.451_453delinsAAG XP_011523396.1:p.Gln151Lys
XM_011525094.2:c.451_453delinsAAG XP_011523396.1:p.Gln151Lys
XM_017024914.1:c.451_453delinsAAG XP_016880403.1:p.Gln151Lys
XM_017024915.1:c.451_453delinsAAG XP_016880404.1:p.Gln151Lys
XM_017024916.1:c.451_453delinsAAG XP_016880405.1:p.Gln151Lys
XM_017024917.1:c.451_453delinsAAG XP_016880406.1:p.Gln151Lys
XM_017024918.2:c.451_453delinsAAG XP_016880407.1:p.Gln151Lys
XM_017024919.1:c.451_453delinsAAG XP_016880408.1:p.Gln151Lys
XR_934513.1:n.1020_1022delinsAAG
XR_934513.3:n.1451_1453delinsAAG
XR_934514.1:n.1020_1022delinsAAG
XR_934514.3:n.1451_1453delinsAAG