Canonical Allele Identifier: CA3057243035
Community Standard Title: NM_058216.3(RAD51C):c.873_874delinsCG (p.Arg292Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720781_58720782delinsCG , CM000679.2:g.58720781_58720782delinsCG GRCh38
NC_000017.10:g.56798142_56798143delinsCG , CM000679.1:g.56798142_56798143delinsCG GRCh37
NC_000017.9:g.54153141_54153142delinsCG NCBI36
NG_023199.1:g.33180_33181delinsCG , LRG_314:g.33180_33181delinsCG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.873_874delinsCG MANE Select NP_478123.1:p.Arg292Gly
ENST00000337432.9:c.873_874delinsCG MANE Select ENSP00000336701.4:p.Arg292Gly
NM_058216.2:c.873_874delinsCG NP_478123.1:p.Arg292Gly
NR_103872.1:n.777_778delinsCG
NR_103872.2:n.748_749delinsCG
ENST00000337432.8:c.873_874delinsCG ENSP00000336701.4:p.Arg292Gly
ENST00000413590.5:c.511_512delinsCG
ENST00000461271.6:c.522_523delinsCG ENSP00000464056.2:p.Arg175Gly
ENST00000475762.5:c.*1541-3259_*1541-3258delinsCG ENSP00000432421.1:n.*1541-3259_*1541-3258delinsCG
ENST00000482007.5:c.*301_*302delinsCG ENSP00000433332.1:n.*301_*302delinsCG
ENST00000487525.5:c.*446_*447delinsCG ENSP00000431637.1:n.*446_*447delinsCG
ENST00000578151.1:n.208_209delinsCG
ENST00000581221.5:n.388_389delinsCG
ENST00000583539.5:c.873_874delinsCG ENSP00000463121.1:p.Arg292Gly
ENST00000584617.5:c.595_596delinsCG
ENST00000584804.1:c.168_169delinsCG ENSP00000463658.1:p.Arg57Gly
ENST00000697678.1:n.775_776delinsCG
ENST00000697679.1:n.1947_1948delinsCG
ENST00000697680.1:c.*1837_*1838delinsCG ENSP00000513392.1:n.*1837_*1838delinsCG
ENST00000697681.1:c.*2034_*2035delinsCG ENSP00000513393.1:n.*2034_*2035delinsCG
ENST00000697683.1:c.*1737_*1738delinsCG ENSP00000513395.1:n.*1737_*1738delinsCG
ENST00000697684.1:n.933_934delinsCG
ENST00000697685.1:c.*1570_*1571delinsCG ENSP00000513396.1:n.*1570_*1571delinsCG
ENST00000697686.1:c.522_523delinsCG ENSP00000513397.1:p.Arg175Gly
ENST00000697687.1:n.752_753delinsCG
ENST00000697688.1:n.919_920delinsCG
ENST00000697689.1:c.*1409_*1410delinsCG ENSP00000513398.1:n.*1409_*1410delinsCG
ENST00000697690.1:c.873_874delinsCG ENSP00000513399.1:p.Arg292Gly
ENST00000697691.1:c.*845_*846delinsCG ENSP00000513400.1:n.*845_*846delinsCG
ENST00000697692.1:c.*885_*886delinsCG ENSP00000513401.1:n.*885_*886delinsCG
ENST00000697694.1:c.522_523delinsCG ENSP00000513402.1:p.Arg175Gly
ENST00000697695.1:n.1480_1481delinsCG
XM_006722001.2:c.873_874delinsCG XP_006722064.1:p.Arg292Gly
XM_006722001.4:c.873_874delinsCG XP_006722064.1:p.Arg292Gly
XM_006722002.2:c.873_874delinsCG XP_006722065.1:p.Arg292Gly
XM_006722002.4:c.873_874delinsCG XP_006722065.1:p.Arg292Gly
XM_006722004.2:c.522_523delinsCG XP_006722067.1:p.Arg175Gly
XM_006722004.3:c.522_523delinsCG XP_006722067.1:p.Arg175Gly
XM_006722005.2:c.522_523delinsCG XP_006722068.1:p.Arg175Gly
XM_006722005.3:c.522_523delinsCG XP_006722068.1:p.Arg175Gly
XM_011525092.1:c.522_523delinsCG XP_011523394.1:p.Arg175Gly
XM_011525092.2:c.522_523delinsCG XP_011523394.1:p.Arg175Gly
XM_011525093.1:c.522_523delinsCG XP_011523395.1:p.Arg175Gly
XM_011525093.2:c.522_523delinsCG XP_011523395.1:p.Arg175Gly
XM_011525094.1:c.522_523delinsCG XP_011523396.1:p.Arg175Gly
XM_011525094.2:c.522_523delinsCG XP_011523396.1:p.Arg175Gly
XM_017024914.1:c.522_523delinsCG XP_016880403.1:p.Arg175Gly
XM_017024915.1:c.522_523delinsCG XP_016880404.1:p.Arg175Gly
XM_017024916.1:c.522_523delinsCG XP_016880405.1:p.Arg175Gly
XM_017024917.1:c.522_523delinsCG XP_016880406.1:p.Arg175Gly
XM_017024918.2:c.522_523delinsCG XP_016880407.1:p.Arg175Gly
XM_017024919.1:c.522_523delinsCG XP_016880408.1:p.Arg175Gly
XR_934513.1:n.1091_1092delinsCG
XR_934513.3:n.1522_1523delinsCG
XR_934514.1:n.1091_1092delinsCG
XR_934514.3:n.1522_1523delinsCG