Canonical Allele Identifier: CA3261179001
Community Standard Title: NM_058216.3(RAD51C):c.727_729delinsAGC (p.Gly243Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709880_58709882delinsAGC , CM000679.2:g.58709880_58709882delinsAGC GRCh38
NC_000017.10:g.56787241_56787243delinsAGC , CM000679.1:g.56787241_56787243delinsAGC GRCh37
NC_000017.9:g.54142240_54142242delinsAGC NCBI36
NG_023199.1:g.22279_22281delinsAGC , LRG_314:g.22279_22281delinsAGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.727_729delinsAGC MANE Select NP_478123.1:p.Gly243Ser
ENST00000337432.9:c.727_729delinsAGC MANE Select ENSP00000336701.4:p.Gly243Ser
NM_058216.2:c.727_729delinsAGC NP_478123.1:p.Gly243Ser
NR_103872.1:n.631_633delinsAGC
NR_103872.2:n.602_604delinsAGC
ENST00000337432.8:c.727_729delinsAGC ENSP00000336701.4:p.Gly243Ser
ENST00000413590.5:c.365_367delinsAGC
ENST00000461271.5:c.376_378delinsAGC ENSP00000464056.1:p.Gly126Ser
ENST00000461271.6:c.376_378delinsAGC ENSP00000464056.2:p.Gly126Ser
ENST00000475762.5:c.*1430_*1432delinsAGC ENSP00000432421.1:n.*1430_*1432delinsAGC
ENST00000482007.5:c.*155_*157delinsAGC ENSP00000433332.1:n.*155_*157delinsAGC
ENST00000487525.5:c.*300_*302delinsAGC ENSP00000431637.1:n.*300_*302delinsAGC
ENST00000578151.1:n.62_64delinsAGC
ENST00000581221.5:n.242_244delinsAGC
ENST00000583539.5:c.727_729delinsAGC ENSP00000463121.1:p.Gly243Ser
ENST00000584617.5:c.449_451delinsAGC
ENST00000584804.1:c.22_24delinsAGC ENSP00000463658.1:p.Gly8Ser
ENST00000697678.1:n.629_631delinsAGC
ENST00000697679.1:n.1801_1803delinsAGC
ENST00000697680.1:c.*1591_*1593delinsAGC ENSP00000513392.1:n.*1591_*1593delinsAGC
ENST00000697681.1:c.*1888_*1890delinsAGC ENSP00000513393.1:n.*1888_*1890delinsAGC
ENST00000697683.1:c.*1591_*1593delinsAGC ENSP00000513395.1:n.*1591_*1593delinsAGC
ENST00000697684.1:n.787_789delinsAGC
ENST00000697685.1:c.*1424_*1426delinsAGC ENSP00000513396.1:n.*1424_*1426delinsAGC
ENST00000697686.1:c.376_378delinsAGC ENSP00000513397.1:p.Gly126Ser
ENST00000697687.1:n.606_608delinsAGC
ENST00000697688.1:n.773_775delinsAGC
ENST00000697689.1:c.*1263_*1265delinsAGC ENSP00000513398.1:n.*1263_*1265delinsAGC
ENST00000697690.1:c.727_729delinsAGC ENSP00000513399.1:p.Gly243Ser
ENST00000697691.1:c.*699_*701delinsAGC ENSP00000513400.1:n.*699_*701delinsAGC
ENST00000697692.1:c.*739_*741delinsAGC ENSP00000513401.1:n.*739_*741delinsAGC
ENST00000697694.1:c.376_378delinsAGC ENSP00000513402.1:p.Gly126Ser
ENST00000697695.1:n.1334_1336delinsAGC
XM_006722001.2:c.727_729delinsAGC XP_006722064.1:p.Gly243Ser
XM_006722001.4:c.727_729delinsAGC XP_006722064.1:p.Gly243Ser
XM_006722002.2:c.727_729delinsAGC XP_006722065.1:p.Gly243Ser
XM_006722002.4:c.727_729delinsAGC XP_006722065.1:p.Gly243Ser
XM_006722004.2:c.376_378delinsAGC XP_006722067.1:p.Gly126Ser
XM_006722004.3:c.376_378delinsAGC XP_006722067.1:p.Gly126Ser
XM_006722005.2:c.376_378delinsAGC XP_006722068.1:p.Gly126Ser
XM_006722005.3:c.376_378delinsAGC XP_006722068.1:p.Gly126Ser
XM_011525092.1:c.376_378delinsAGC XP_011523394.1:p.Gly126Ser
XM_011525092.2:c.376_378delinsAGC XP_011523394.1:p.Gly126Ser
XM_011525093.1:c.376_378delinsAGC XP_011523395.1:p.Gly126Ser
XM_011525093.2:c.376_378delinsAGC XP_011523395.1:p.Gly126Ser
XM_011525094.1:c.376_378delinsAGC XP_011523396.1:p.Gly126Ser
XM_011525094.2:c.376_378delinsAGC XP_011523396.1:p.Gly126Ser
XM_017024914.1:c.376_378delinsAGC XP_016880403.1:p.Gly126Ser
XM_017024915.1:c.376_378delinsAGC XP_016880404.1:p.Gly126Ser
XM_017024916.1:c.376_378delinsAGC XP_016880405.1:p.Gly126Ser
XM_017024917.1:c.376_378delinsAGC XP_016880406.1:p.Gly126Ser
XM_017024918.2:c.376_378delinsAGC XP_016880407.1:p.Gly126Ser
XM_017024919.1:c.376_378delinsAGC XP_016880408.1:p.Gly126Ser
XR_934513.1:n.945_947delinsAGC
XR_934513.3:n.1376_1378delinsAGC
XR_934514.1:n.945_947delinsAGC
XR_934514.3:n.1376_1378delinsAGC