Canonical Allele Identifier: CA3261178665
Community Standard Title: NM_058216.3(RAD51C):c.577_579delinsGGC (p.Arg193Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703201_58703203delinsGGC , CM000679.2:g.58703201_58703203delinsGGC GRCh38
NC_000017.10:g.56780562_56780564delinsGGC , CM000679.1:g.56780562_56780564delinsGGC GRCh37
NC_000017.9:g.54135561_54135563delinsGGC NCBI36
NG_023199.1:g.15600_15602delinsGGC , LRG_314:g.15600_15602delinsGGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.577_579delinsGGC MANE Select NP_478123.1:p.Arg193Gly
ENST00000337432.9:c.577_579delinsGGC MANE Select ENSP00000336701.4:p.Arg193Gly
NM_058216.2:c.577_579delinsGGC NP_478123.1:p.Arg193Gly
NR_103872.1:n.481_483delinsGGC
NR_103872.2:n.452_454delinsGGC
ENST00000337432.8:c.577_579delinsGGC ENSP00000336701.4:p.Arg193Gly
ENST00000413590.5:c.215_217delinsGGC
ENST00000425173.5:c.373_375delinsGGC ENSP00000407282.1:p.Arg125Gly
ENST00000461271.5:c.226_228delinsGGC ENSP00000464056.1:p.Arg76Gly
ENST00000461271.6:c.226_228delinsGGC ENSP00000464056.2:p.Arg76Gly
ENST00000475762.5:c.*1280_*1282delinsGGC ENSP00000432421.1:n.*1280_*1282delinsGGC
ENST00000482007.5:c.*5_*7delinsGGC ENSP00000433332.1:n.*5_*7delinsGGC
ENST00000487525.5:c.*5_*7delinsGGC ENSP00000431637.1:n.*5_*7delinsGGC
ENST00000487921.5:n.489_491delinsGGC
ENST00000583539.5:c.577_579delinsGGC ENSP00000463121.1:p.Arg193Gly
ENST00000584617.5:c.299_301delinsGGC
ENST00000697677.1:n.1658_1660delinsGGC
ENST00000697678.1:n.479_481delinsGGC
ENST00000697679.1:n.1651_1653delinsGGC
ENST00000697680.1:c.*1441_*1443delinsGGC ENSP00000513392.1:n.*1441_*1443delinsGGC
ENST00000697681.1:c.*1593_*1595delinsGGC ENSP00000513393.1:n.*1593_*1595delinsGGC
ENST00000697683.1:c.*1441_*1443delinsGGC ENSP00000513395.1:n.*1441_*1443delinsGGC
ENST00000697684.1:n.637_639delinsGGC
ENST00000697685.1:c.*1274_*1276delinsGGC ENSP00000513396.1:n.*1274_*1276delinsGGC
ENST00000697686.1:c.226_228delinsGGC ENSP00000513397.1:p.Arg76Gly
ENST00000697687.1:n.456_458delinsGGC
ENST00000697688.1:n.623_625delinsGGC
ENST00000697689.1:c.*1113_*1115delinsGGC ENSP00000513398.1:n.*1113_*1115delinsGGC
ENST00000697690.1:c.577_579delinsGGC ENSP00000513399.1:p.Arg193Gly
ENST00000697691.1:c.*549_*551delinsGGC ENSP00000513400.1:n.*549_*551delinsGGC
ENST00000697692.1:c.*589_*591delinsGGC ENSP00000513401.1:n.*589_*591delinsGGC
ENST00000697694.1:c.226_228delinsGGC ENSP00000513402.1:p.Arg76Gly
ENST00000697695.1:n.1184_1186delinsGGC
XM_006722001.2:c.577_579delinsGGC XP_006722064.1:p.Arg193Gly
XM_006722001.4:c.577_579delinsGGC XP_006722064.1:p.Arg193Gly
XM_006722002.2:c.577_579delinsGGC XP_006722065.1:p.Arg193Gly
XM_006722002.4:c.577_579delinsGGC XP_006722065.1:p.Arg193Gly
XM_006722004.2:c.226_228delinsGGC XP_006722067.1:p.Arg76Gly
XM_006722004.3:c.226_228delinsGGC XP_006722067.1:p.Arg76Gly
XM_006722005.2:c.226_228delinsGGC XP_006722068.1:p.Arg76Gly
XM_006722005.3:c.226_228delinsGGC XP_006722068.1:p.Arg76Gly
XM_011525092.1:c.226_228delinsGGC XP_011523394.1:p.Arg76Gly
XM_011525092.2:c.226_228delinsGGC XP_011523394.1:p.Arg76Gly
XM_011525093.1:c.226_228delinsGGC XP_011523395.1:p.Arg76Gly
XM_011525093.2:c.226_228delinsGGC XP_011523395.1:p.Arg76Gly
XM_011525094.1:c.226_228delinsGGC XP_011523396.1:p.Arg76Gly
XM_011525094.2:c.226_228delinsGGC XP_011523396.1:p.Arg76Gly
XM_017024914.1:c.226_228delinsGGC XP_016880403.1:p.Arg76Gly
XM_017024915.1:c.226_228delinsGGC XP_016880404.1:p.Arg76Gly
XM_017024916.1:c.226_228delinsGGC XP_016880405.1:p.Arg76Gly
XM_017024917.1:c.226_228delinsGGC XP_016880406.1:p.Arg76Gly
XM_017024918.2:c.226_228delinsGGC XP_016880407.1:p.Arg76Gly
XM_017024919.1:c.226_228delinsGGC XP_016880408.1:p.Arg76Gly
XR_934513.1:n.650_652delinsGGC
XR_934513.3:n.1081_1083delinsGGC
XR_934514.1:n.650_652delinsGGC
XR_934514.3:n.1081_1083delinsGGC