Canonical Allele Identifier: CA3060598405
Community Standard Title: NM_058216.3(RAD51C):c.634_636delinsGGA (p.Arg212Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703258_58703260delinsGGA , CM000679.2:g.58703258_58703260delinsGGA GRCh38
NC_000017.10:g.56780619_56780621delinsGGA , CM000679.1:g.56780619_56780621delinsGGA GRCh37
NC_000017.9:g.54135618_54135620delinsGGA NCBI36
NG_023199.1:g.15657_15659delinsGGA , LRG_314:g.15657_15659delinsGGA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.634_636delinsGGA MANE Select NP_478123.1:p.Arg212Gly
ENST00000337432.9:c.634_636delinsGGA MANE Select ENSP00000336701.4:p.Arg212Gly
NM_058216.2:c.634_636delinsGGA NP_478123.1:p.Arg212Gly
NR_103872.1:n.538_540delinsGGA
NR_103872.2:n.509_511delinsGGA
ENST00000337432.8:c.634_636delinsGGA ENSP00000336701.4:p.Arg212Gly
ENST00000413590.5:c.272_274delinsGGA
ENST00000425173.5:c.430_432delinsGGA ENSP00000407282.1:p.Arg144Gly
ENST00000461271.5:c.283_285delinsGGA ENSP00000464056.1:p.Arg95Gly
ENST00000461271.6:c.283_285delinsGGA ENSP00000464056.2:p.Arg95Gly
ENST00000475762.5:c.*1337_*1339delinsGGA ENSP00000432421.1:n.*1337_*1339delinsGGA
ENST00000482007.5:c.*62_*64delinsGGA ENSP00000433332.1:n.*62_*64delinsGGA
ENST00000487525.5:c.*62_*64delinsGGA ENSP00000431637.1:n.*62_*64delinsGGA
ENST00000487921.5:n.546_548delinsGGA
ENST00000583539.5:c.634_636delinsGGA ENSP00000463121.1:p.Arg212Gly
ENST00000584617.5:c.356_358delinsGGA
ENST00000697677.1:n.1715_1717delinsGGA
ENST00000697678.1:n.536_538delinsGGA
ENST00000697679.1:n.1708_1710delinsGGA
ENST00000697680.1:c.*1498_*1500delinsGGA ENSP00000513392.1:n.*1498_*1500delinsGGA
ENST00000697681.1:c.*1650_*1652delinsGGA ENSP00000513393.1:n.*1650_*1652delinsGGA
ENST00000697683.1:c.*1498_*1500delinsGGA ENSP00000513395.1:n.*1498_*1500delinsGGA
ENST00000697684.1:n.694_696delinsGGA
ENST00000697685.1:c.*1331_*1333delinsGGA ENSP00000513396.1:n.*1331_*1333delinsGGA
ENST00000697686.1:c.283_285delinsGGA ENSP00000513397.1:p.Arg95Gly
ENST00000697687.1:n.513_515delinsGGA
ENST00000697688.1:n.680_682delinsGGA
ENST00000697689.1:c.*1170_*1172delinsGGA ENSP00000513398.1:n.*1170_*1172delinsGGA
ENST00000697690.1:c.634_636delinsGGA ENSP00000513399.1:p.Arg212Gly
ENST00000697691.1:c.*606_*608delinsGGA ENSP00000513400.1:n.*606_*608delinsGGA
ENST00000697692.1:c.*646_*648delinsGGA ENSP00000513401.1:n.*646_*648delinsGGA
ENST00000697694.1:c.283_285delinsGGA ENSP00000513402.1:p.Arg95Gly
ENST00000697695.1:n.1241_1243delinsGGA
XM_006722001.2:c.634_636delinsGGA XP_006722064.1:p.Arg212Gly
XM_006722001.4:c.634_636delinsGGA XP_006722064.1:p.Arg212Gly
XM_006722002.2:c.634_636delinsGGA XP_006722065.1:p.Arg212Gly
XM_006722002.4:c.634_636delinsGGA XP_006722065.1:p.Arg212Gly
XM_006722004.2:c.283_285delinsGGA XP_006722067.1:p.Arg95Gly
XM_006722004.3:c.283_285delinsGGA XP_006722067.1:p.Arg95Gly
XM_006722005.2:c.283_285delinsGGA XP_006722068.1:p.Arg95Gly
XM_006722005.3:c.283_285delinsGGA XP_006722068.1:p.Arg95Gly
XM_011525092.1:c.283_285delinsGGA XP_011523394.1:p.Arg95Gly
XM_011525092.2:c.283_285delinsGGA XP_011523394.1:p.Arg95Gly
XM_011525093.1:c.283_285delinsGGA XP_011523395.1:p.Arg95Gly
XM_011525093.2:c.283_285delinsGGA XP_011523395.1:p.Arg95Gly
XM_011525094.1:c.283_285delinsGGA XP_011523396.1:p.Arg95Gly
XM_011525094.2:c.283_285delinsGGA XP_011523396.1:p.Arg95Gly
XM_017024914.1:c.283_285delinsGGA XP_016880403.1:p.Arg95Gly
XM_017024915.1:c.283_285delinsGGA XP_016880404.1:p.Arg95Gly
XM_017024916.1:c.283_285delinsGGA XP_016880405.1:p.Arg95Gly
XM_017024917.1:c.283_285delinsGGA XP_016880406.1:p.Arg95Gly
XM_017024918.2:c.283_285delinsGGA XP_016880407.1:p.Arg95Gly
XM_017024919.1:c.283_285delinsGGA XP_016880408.1:p.Arg95Gly
XR_934513.1:n.707_709delinsGGA
XR_934513.3:n.1138_1140delinsGGA
XR_934514.1:n.707_709delinsGGA
XR_934514.3:n.1138_1140delinsGGA