Canonical Allele Identifier: CA3057243397
Community Standard Title: NM_058216.3(RAD51C):c.1054_1055delinsGA (p.Thr352Asp)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734145_58734146delinsGA , CM000679.2:g.58734145_58734146delinsGA GRCh38
NC_000017.10:g.56811506_56811507delinsGA , CM000679.1:g.56811506_56811507delinsGA GRCh37
NC_000017.9:g.54166505_54166506delinsGA NCBI36
NG_023199.1:g.46544_46545delinsGA , LRG_314:g.46544_46545delinsGA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1054_1055delinsGA MANE Select NP_478123.1:p.Thr352Asp
ENST00000337432.9:c.1054_1055delinsGA MANE Select ENSP00000336701.4:p.Thr352Asp
NM_058216.2:c.1054_1055delinsGA NP_478123.1:p.Thr352Asp
NR_103872.1:n.958_959delinsGA
NR_103872.2:n.929_930delinsGA
ENST00000337432.8:c.1054_1055delinsGA ENSP00000336701.4:p.Thr352Asp
ENST00000413590.5:c.695_696delinsGA
ENST00000461271.6:c.*1586_*1587delinsGA ENSP00000464056.2:n.*1586_*1587delinsGA
ENST00000461706.1:n.241_242delinsGA
ENST00000475762.5:c.*1690_*1691delinsGA ENSP00000432421.1:n.*1690_*1691delinsGA
ENST00000482007.5:c.*482_*483delinsGA ENSP00000433332.1:n.*482_*483delinsGA
ENST00000487525.5:c.*630_*631delinsGA ENSP00000431637.1:n.*630_*631delinsGA
ENST00000578151.1:n.267_268delinsGA
ENST00000581221.5:n.569_570delinsGA
ENST00000584804.1:c.288_289delinsGA ENSP00000463658.1:p.Leu97Ile
ENST00000697680.1:c.*2018_*2019delinsGA ENSP00000513392.1:n.*2018_*2019delinsGA
ENST00000697681.1:c.*2215_*2216delinsGA ENSP00000513393.1:n.*2215_*2216delinsGA
ENST00000697683.1:c.*1990_*1991delinsGA ENSP00000513395.1:n.*1990_*1991delinsGA
ENST00000697685.1:c.*1751_*1752delinsGA ENSP00000513396.1:n.*1751_*1752delinsGA
ENST00000697686.1:c.825_826delinsGA ENSP00000513397.1:p.Leu276Ile
ENST00000697689.1:c.*1468_*1469delinsGA ENSP00000513398.1:n.*1468_*1469delinsGA
ENST00000697690.1:c.*14_*15delinsGA ENSP00000513399.1:n.*14_*15delinsGA
ENST00000697691.1:c.*1026_*1027delinsGA ENSP00000513400.1:n.*1026_*1027delinsGA
ENST00000697692.1:c.*1066_*1067delinsGA ENSP00000513401.1:n.*1066_*1067delinsGA
ENST00000697694.1:c.703_704delinsGA ENSP00000513402.1:p.Thr235Asp
ENST00000697695.1:n.1661_1662delinsGA
XM_006722001.2:c.1057_1058delinsGA XP_006722064.1:p.Thr353Asp
XM_006722001.4:c.1057_1058delinsGA XP_006722064.1:p.Thr353Asp
XM_006722002.2:c.993_994delinsGA XP_006722065.1:p.Leu332Ile
XM_006722002.4:c.993_994delinsGA XP_006722065.1:p.Leu332Ile
XM_006722004.2:c.706_707delinsGA XP_006722067.1:p.Thr236Asp
XM_006722004.3:c.706_707delinsGA XP_006722067.1:p.Thr236Asp
XM_006722005.2:c.706_707delinsGA XP_006722068.1:p.Thr236Asp
XM_006722005.3:c.706_707delinsGA XP_006722068.1:p.Thr236Asp
XM_011525092.1:c.706_707delinsGA XP_011523394.1:p.Thr236Asp
XM_011525092.2:c.706_707delinsGA XP_011523394.1:p.Thr236Asp
XM_011525093.1:c.706_707delinsGA XP_011523395.1:p.Thr236Asp
XM_011525093.2:c.706_707delinsGA XP_011523395.1:p.Thr236Asp
XM_011525094.1:c.706_707delinsGA XP_011523396.1:p.Thr236Asp
XM_011525094.2:c.706_707delinsGA XP_011523396.1:p.Thr236Asp
XM_017024914.1:c.703_704delinsGA XP_016880403.1:p.Thr235Asp
XM_017024915.1:c.703_704delinsGA XP_016880404.1:p.Thr235Asp
XM_017024916.1:c.703_704delinsGA XP_016880405.1:p.Thr235Asp
XM_017024917.1:c.703_704delinsGA XP_016880406.1:p.Thr235Asp
XM_017024918.2:c.703_704delinsGA XP_016880407.1:p.Thr235Asp
XM_017024919.1:c.642_643delinsGA XP_016880408.1:p.Leu215Ile
XR_934513.1:n.1272_1273delinsGA
XR_934513.3:n.1703_1704delinsGA
XR_934514.1:n.1275_1276delinsGA
XR_934514.3:n.1706_1707delinsGA
XR_934886.1:n.149+3925_149+3926delinsTC
XR_934886.2:n.149+3925_149+3926delinsTC