Canonical Allele Identifier: CA3261179282
Community Standard Title: NM_058216.3(RAD51C):c.52_54delinsAGC (p.Pro18Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692695_58692697delinsAGC , CM000679.2:g.58692695_58692697delinsAGC GRCh38
NC_000017.10:g.56770056_56770058delinsAGC , CM000679.1:g.56770056_56770058delinsAGC GRCh37
NC_000017.9:g.54125055_54125057delinsAGC NCBI36
NG_023199.1:g.5094_5096delinsAGC , LRG_314:g.5094_5096delinsAGC
NG_047169.1:g.4383_4385delinsGCT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.52_54delinsAGC MANE Select NP_478123.1:p.Pro18Ser
ENST00000337432.9:c.52_54delinsAGC MANE Select ENSP00000336701.4:p.Pro18Ser
NM_002876.3:c.52_54delinsAGC NP_002867.1:p.Pro18Ser
NM_002876.4:c.52_54delinsAGC NP_002867.1:p.Pro18Ser
NM_058216.2:c.52_54delinsAGC NP_478123.1:p.Pro18Ser
NR_103872.1:n.123_125delinsAGC
NR_103872.2:n.94_96delinsAGC
NR_103873.1:n.113+10_113+12delinsAGC
ENST00000337432.8:c.52_54delinsAGC ENSP00000336701.4:p.Pro18Ser
ENST00000421782.3:c.52_54delinsAGC ENSP00000391450.2:p.Pro18Ser
ENST00000461271.5:c.-207+10_-207+12delinsAGC ENSP00000464056.1:n.-207+10_-207+12delinsAGC
ENST00000461271.6:c.-207+10_-207+12delinsAGC ENSP00000464056.2:n.-207+10_-207+12delinsAGC
ENST00000475762.5:c.52_54delinsAGC ENSP00000432421.1:p.Pro18Ser
ENST00000476741.2:n.94_96delinsAGC
ENST00000482007.5:c.52_54delinsAGC ENSP00000433332.1:p.Pro18Ser
ENST00000486827.1:c.52_54delinsAGC ENSP00000436761.1:p.Pro18Ser
ENST00000487525.5:c.52_54delinsAGC ENSP00000431637.1:p.Pro18Ser
ENST00000487921.5:n.57+63_57+65delinsAGC
ENST00000583539.5:c.52_54delinsAGC ENSP00000463121.1:p.Pro18Ser
ENST00000584617.5:c.33_35delinsAGC
ENST00000697675.1:n.123_125delinsAGC
ENST00000697676.1:n.112_114delinsAGC
ENST00000697677.1:n.110_112delinsAGC
ENST00000697678.1:n.47+63_47+65delinsAGC
ENST00000697679.1:n.103_105delinsAGC
ENST00000697680.1:c.52_54delinsAGC ENSP00000513392.1:p.Pro18Ser
ENST00000697681.1:c.52_54delinsAGC ENSP00000513393.1:p.Pro18Ser
ENST00000697683.1:c.52_54delinsAGC ENSP00000513395.1:p.Pro18Ser
ENST00000697684.1:n.112_114delinsAGC
ENST00000697685.1:c.52_54delinsAGC ENSP00000513396.1:p.Pro18Ser
ENST00000697686.1:c.-207+63_-207+65delinsAGC ENSP00000513397.1:n.-207+63_-207+65delinsAGC
ENST00000697687.1:n.98_100delinsAGC
ENST00000697688.1:n.98_100delinsAGC
ENST00000697689.1:c.52_54delinsAGC ENSP00000513398.1:p.Pro18Ser
ENST00000697690.1:c.52_54delinsAGC ENSP00000513399.1:p.Pro18Ser
ENST00000697691.1:c.42+10_42+12delinsAGC ENSP00000513400.1:n.42+10_42+12delinsAGC
ENST00000697692.1:c.52_54delinsAGC ENSP00000513401.1:p.Pro18Ser
XM_006722001.2:c.52_54delinsAGC XP_006722064.1:p.Pro18Ser
XM_006722001.4:c.52_54delinsAGC XP_006722064.1:p.Pro18Ser
XM_006722002.2:c.52_54delinsAGC XP_006722065.1:p.Pro18Ser
XM_006722002.4:c.52_54delinsAGC XP_006722065.1:p.Pro18Ser
XM_006722004.2:c.-207+10_-207+12delinsAGC XP_006722067.1:n.-207+10_-207+12delinsAGC
XM_006722004.3:c.-207+10_-207+12delinsAGC XP_006722067.1:n.-207+10_-207+12delinsAGC
XM_006722005.2:c.-207+63_-207+65delinsAGC XP_006722068.1:n.-207+63_-207+65delinsAGC
XM_006722005.3:c.-207+63_-207+65delinsAGC XP_006722068.1:n.-207+63_-207+65delinsAGC
XM_011525092.1:c.-507+10_-507+12delinsAGC XP_011523394.1:n.-507+10_-507+12delinsAGC
XM_011525092.2:c.-507+10_-507+12delinsAGC XP_011523394.1:n.-507+10_-507+12delinsAGC
XM_011525093.1:c.-668+10_-668+12delinsAGC XP_011523395.1:n.-668+10_-668+12delinsAGC
XM_011525093.2:c.-668+10_-668+12delinsAGC XP_011523395.1:n.-668+10_-668+12delinsAGC
XM_017024914.1:c.-207+10_-207+12delinsAGC XP_016880403.1:n.-207+10_-207+12delinsAGC
XM_017024916.1:c.-507+10_-507+12delinsAGC XP_016880405.1:n.-507+10_-507+12delinsAGC
XM_017024917.1:c.-207+63_-207+65delinsAGC XP_016880406.1:n.-207+63_-207+65delinsAGC
XM_017024918.2:c.-471_-469delinsAGC XP_016880407.1:n.-471_-469delinsAGC
XM_017024919.1:c.-668+10_-668+12delinsAGC XP_016880408.1:n.-668+10_-668+12delinsAGC
XR_934513.1:n.125_127delinsAGC
XR_934513.3:n.556_558delinsAGC
XR_934514.1:n.125_127delinsAGC
XR_934514.3:n.556_558delinsAGC