Canonical Allele Identifier: CA3261178951
Community Standard Title: NM_058216.3(RAD51C):c.874_876delinsGGC (p.Arg292Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720782_58720784delinsGGC , CM000679.2:g.58720782_58720784delinsGGC GRCh38
NC_000017.10:g.56798143_56798145delinsGGC , CM000679.1:g.56798143_56798145delinsGGC GRCh37
NC_000017.9:g.54153142_54153144delinsGGC NCBI36
NG_023199.1:g.33181_33183delinsGGC , LRG_314:g.33181_33183delinsGGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.874_876delinsGGC MANE Select NP_478123.1:p.Arg292Gly
ENST00000337432.9:c.874_876delinsGGC MANE Select ENSP00000336701.4:p.Arg292Gly
NM_058216.2:c.874_876delinsGGC NP_478123.1:p.Arg292Gly
NR_103872.1:n.778_780delinsGGC
NR_103872.2:n.749_751delinsGGC
ENST00000337432.8:c.874_876delinsGGC ENSP00000336701.4:p.Arg292Gly
ENST00000413590.5:c.512_514delinsGGC
ENST00000461271.6:c.523_525delinsGGC ENSP00000464056.2:p.Arg175Gly
ENST00000475762.5:c.*1541-3258_*1541-3256delinsGGC ENSP00000432421.1:n.*1541-3258_*1541-3256delinsGGC
ENST00000482007.5:c.*302_*304delinsGGC ENSP00000433332.1:n.*302_*304delinsGGC
ENST00000487525.5:c.*447_*449delinsGGC ENSP00000431637.1:n.*447_*449delinsGGC
ENST00000578151.1:n.209_211delinsGGC
ENST00000581221.5:n.389_391delinsGGC
ENST00000583539.5:c.874_876delinsGGC ENSP00000463121.1:p.Arg292Gly
ENST00000584617.5:c.596_598delinsGGC
ENST00000584804.1:c.169_171delinsGGC ENSP00000463658.1:p.Arg57Gly
ENST00000697678.1:n.776_778delinsGGC
ENST00000697679.1:n.1948_1950delinsGGC
ENST00000697680.1:c.*1838_*1840delinsGGC ENSP00000513392.1:n.*1838_*1840delinsGGC
ENST00000697681.1:c.*2035_*2037delinsGGC ENSP00000513393.1:n.*2035_*2037delinsGGC
ENST00000697683.1:c.*1738_*1740delinsGGC ENSP00000513395.1:n.*1738_*1740delinsGGC
ENST00000697684.1:n.934_936delinsGGC
ENST00000697685.1:c.*1571_*1573delinsGGC ENSP00000513396.1:n.*1571_*1573delinsGGC
ENST00000697686.1:c.523_525delinsGGC ENSP00000513397.1:p.Arg175Gly
ENST00000697687.1:n.753_755delinsGGC
ENST00000697688.1:n.920_922delinsGGC
ENST00000697689.1:c.*1410_*1412delinsGGC ENSP00000513398.1:n.*1410_*1412delinsGGC
ENST00000697690.1:c.874_876delinsGGC ENSP00000513399.1:p.Arg292Gly
ENST00000697691.1:c.*846_*848delinsGGC ENSP00000513400.1:n.*846_*848delinsGGC
ENST00000697692.1:c.*886_*888delinsGGC ENSP00000513401.1:n.*886_*888delinsGGC
ENST00000697694.1:c.523_525delinsGGC ENSP00000513402.1:p.Arg175Gly
ENST00000697695.1:n.1481_1483delinsGGC
XM_006722001.2:c.874_876delinsGGC XP_006722064.1:p.Arg292Gly
XM_006722001.4:c.874_876delinsGGC XP_006722064.1:p.Arg292Gly
XM_006722002.2:c.874_876delinsGGC XP_006722065.1:p.Arg292Gly
XM_006722002.4:c.874_876delinsGGC XP_006722065.1:p.Arg292Gly
XM_006722004.2:c.523_525delinsGGC XP_006722067.1:p.Arg175Gly
XM_006722004.3:c.523_525delinsGGC XP_006722067.1:p.Arg175Gly
XM_006722005.2:c.523_525delinsGGC XP_006722068.1:p.Arg175Gly
XM_006722005.3:c.523_525delinsGGC XP_006722068.1:p.Arg175Gly
XM_011525092.1:c.523_525delinsGGC XP_011523394.1:p.Arg175Gly
XM_011525092.2:c.523_525delinsGGC XP_011523394.1:p.Arg175Gly
XM_011525093.1:c.523_525delinsGGC XP_011523395.1:p.Arg175Gly
XM_011525093.2:c.523_525delinsGGC XP_011523395.1:p.Arg175Gly
XM_011525094.1:c.523_525delinsGGC XP_011523396.1:p.Arg175Gly
XM_011525094.2:c.523_525delinsGGC XP_011523396.1:p.Arg175Gly
XM_017024914.1:c.523_525delinsGGC XP_016880403.1:p.Arg175Gly
XM_017024915.1:c.523_525delinsGGC XP_016880404.1:p.Arg175Gly
XM_017024916.1:c.523_525delinsGGC XP_016880405.1:p.Arg175Gly
XM_017024917.1:c.523_525delinsGGC XP_016880406.1:p.Arg175Gly
XM_017024918.2:c.523_525delinsGGC XP_016880407.1:p.Arg175Gly
XM_017024919.1:c.523_525delinsGGC XP_016880408.1:p.Arg175Gly
XR_934513.1:n.1092_1094delinsGGC
XR_934513.3:n.1523_1525delinsGGC
XR_934514.1:n.1092_1094delinsGGC
XR_934514.3:n.1523_1525delinsGGC