Canonical Allele Identifier: CA3057242834
Community Standard Title: NM_058216.3(RAD51C):c.727_728delinsTC (p.Gly243Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709880_58709881delinsTC , CM000679.2:g.58709880_58709881delinsTC GRCh38
NC_000017.10:g.56787241_56787242delinsTC , CM000679.1:g.56787241_56787242delinsTC GRCh37
NC_000017.9:g.54142240_54142241delinsTC NCBI36
NG_023199.1:g.22279_22280delinsTC , LRG_314:g.22279_22280delinsTC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.727_728delinsTC MANE Select NP_478123.1:p.Gly243Ser
ENST00000337432.9:c.727_728delinsTC MANE Select ENSP00000336701.4:p.Gly243Ser
NM_058216.2:c.727_728delinsTC NP_478123.1:p.Gly243Ser
NR_103872.1:n.631_632delinsTC
NR_103872.2:n.602_603delinsTC
ENST00000337432.8:c.727_728delinsTC ENSP00000336701.4:p.Gly243Ser
ENST00000413590.5:c.365_366delinsTC
ENST00000461271.5:c.376_377delinsTC ENSP00000464056.1:p.Gly126Ser
ENST00000461271.6:c.376_377delinsTC ENSP00000464056.2:p.Gly126Ser
ENST00000475762.5:c.*1430_*1431delinsTC ENSP00000432421.1:n.*1430_*1431delinsTC
ENST00000482007.5:c.*155_*156delinsTC ENSP00000433332.1:n.*155_*156delinsTC
ENST00000487525.5:c.*300_*301delinsTC ENSP00000431637.1:n.*300_*301delinsTC
ENST00000578151.1:n.62_63delinsTC
ENST00000581221.5:n.242_243delinsTC
ENST00000583539.5:c.727_728delinsTC ENSP00000463121.1:p.Gly243Ser
ENST00000584617.5:c.449_450delinsTC
ENST00000584804.1:c.22_23delinsTC ENSP00000463658.1:p.Gly8Ser
ENST00000697678.1:n.629_630delinsTC
ENST00000697679.1:n.1801_1802delinsTC
ENST00000697680.1:c.*1591_*1592delinsTC ENSP00000513392.1:n.*1591_*1592delinsTC
ENST00000697681.1:c.*1888_*1889delinsTC ENSP00000513393.1:n.*1888_*1889delinsTC
ENST00000697683.1:c.*1591_*1592delinsTC ENSP00000513395.1:n.*1591_*1592delinsTC
ENST00000697684.1:n.787_788delinsTC
ENST00000697685.1:c.*1424_*1425delinsTC ENSP00000513396.1:n.*1424_*1425delinsTC
ENST00000697686.1:c.376_377delinsTC ENSP00000513397.1:p.Gly126Ser
ENST00000697687.1:n.606_607delinsTC
ENST00000697688.1:n.773_774delinsTC
ENST00000697689.1:c.*1263_*1264delinsTC ENSP00000513398.1:n.*1263_*1264delinsTC
ENST00000697690.1:c.727_728delinsTC ENSP00000513399.1:p.Gly243Ser
ENST00000697691.1:c.*699_*700delinsTC ENSP00000513400.1:n.*699_*700delinsTC
ENST00000697692.1:c.*739_*740delinsTC ENSP00000513401.1:n.*739_*740delinsTC
ENST00000697694.1:c.376_377delinsTC ENSP00000513402.1:p.Gly126Ser
ENST00000697695.1:n.1334_1335delinsTC
XM_006722001.2:c.727_728delinsTC XP_006722064.1:p.Gly243Ser
XM_006722001.4:c.727_728delinsTC XP_006722064.1:p.Gly243Ser
XM_006722002.2:c.727_728delinsTC XP_006722065.1:p.Gly243Ser
XM_006722002.4:c.727_728delinsTC XP_006722065.1:p.Gly243Ser
XM_006722004.2:c.376_377delinsTC XP_006722067.1:p.Gly126Ser
XM_006722004.3:c.376_377delinsTC XP_006722067.1:p.Gly126Ser
XM_006722005.2:c.376_377delinsTC XP_006722068.1:p.Gly126Ser
XM_006722005.3:c.376_377delinsTC XP_006722068.1:p.Gly126Ser
XM_011525092.1:c.376_377delinsTC XP_011523394.1:p.Gly126Ser
XM_011525092.2:c.376_377delinsTC XP_011523394.1:p.Gly126Ser
XM_011525093.1:c.376_377delinsTC XP_011523395.1:p.Gly126Ser
XM_011525093.2:c.376_377delinsTC XP_011523395.1:p.Gly126Ser
XM_011525094.1:c.376_377delinsTC XP_011523396.1:p.Gly126Ser
XM_011525094.2:c.376_377delinsTC XP_011523396.1:p.Gly126Ser
XM_017024914.1:c.376_377delinsTC XP_016880403.1:p.Gly126Ser
XM_017024915.1:c.376_377delinsTC XP_016880404.1:p.Gly126Ser
XM_017024916.1:c.376_377delinsTC XP_016880405.1:p.Gly126Ser
XM_017024917.1:c.376_377delinsTC XP_016880406.1:p.Gly126Ser
XM_017024918.2:c.376_377delinsTC XP_016880407.1:p.Gly126Ser
XM_017024919.1:c.376_377delinsTC XP_016880408.1:p.Gly126Ser
XR_934513.1:n.945_946delinsTC
XR_934513.3:n.1376_1377delinsTC
XR_934514.1:n.945_946delinsTC
XR_934514.3:n.1376_1377delinsTC