Canonical Allele Identifier: CA3261180556
Community Standard Title: NM_058216.3(RAD51C):c.832_834delinsAGC (p.Leu278Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709985_58709987delinsAGC , CM000679.2:g.58709985_58709987delinsAGC GRCh38
NC_000017.10:g.56787346_56787348delinsAGC , CM000679.1:g.56787346_56787348delinsAGC GRCh37
NC_000017.9:g.54142345_54142347delinsAGC NCBI36
NG_023199.1:g.22384_22386delinsAGC , LRG_314:g.22384_22386delinsAGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.832_834delinsAGC MANE Select NP_478123.1:p.Leu278Ser
ENST00000337432.9:c.832_834delinsAGC MANE Select ENSP00000336701.4:p.Leu278Ser
NM_058216.2:c.832_834delinsAGC NP_478123.1:p.Leu278Ser
NR_103872.1:n.736_738delinsAGC
NR_103872.2:n.707_709delinsAGC
ENST00000337432.8:c.832_834delinsAGC ENSP00000336701.4:p.Leu278Ser
ENST00000413590.5:c.470_472delinsAGC
ENST00000461271.6:c.481_483delinsAGC ENSP00000464056.2:p.Leu161Ser
ENST00000475762.5:c.*1535_*1537delinsAGC ENSP00000432421.1:n.*1535_*1537delinsAGC
ENST00000482007.5:c.*260_*262delinsAGC ENSP00000433332.1:n.*260_*262delinsAGC
ENST00000487525.5:c.*405_*407delinsAGC ENSP00000431637.1:n.*405_*407delinsAGC
ENST00000578151.1:n.167_169delinsAGC
ENST00000581221.5:n.347_349delinsAGC
ENST00000583539.5:c.832_834delinsAGC ENSP00000463121.1:p.Leu278Ser
ENST00000584617.5:c.554_556delinsAGC
ENST00000584804.1:c.127_129delinsAGC ENSP00000463658.1:p.Leu43Ser
ENST00000697678.1:n.734_736delinsAGC
ENST00000697679.1:n.1906_1908delinsAGC
ENST00000697680.1:c.*1696_*1698delinsAGC ENSP00000513392.1:n.*1696_*1698delinsAGC
ENST00000697681.1:c.*1993_*1995delinsAGC ENSP00000513393.1:n.*1993_*1995delinsAGC
ENST00000697683.1:c.*1696_*1698delinsAGC ENSP00000513395.1:n.*1696_*1698delinsAGC
ENST00000697684.1:n.892_894delinsAGC
ENST00000697685.1:c.*1529_*1531delinsAGC ENSP00000513396.1:n.*1529_*1531delinsAGC
ENST00000697686.1:c.481_483delinsAGC ENSP00000513397.1:p.Leu161Ser
ENST00000697687.1:n.711_713delinsAGC
ENST00000697688.1:n.878_880delinsAGC
ENST00000697689.1:c.*1368_*1370delinsAGC ENSP00000513398.1:n.*1368_*1370delinsAGC
ENST00000697690.1:c.832_834delinsAGC ENSP00000513399.1:p.Leu278Ser
ENST00000697691.1:c.*804_*806delinsAGC ENSP00000513400.1:n.*804_*806delinsAGC
ENST00000697692.1:c.*844_*846delinsAGC ENSP00000513401.1:n.*844_*846delinsAGC
ENST00000697694.1:c.481_483delinsAGC ENSP00000513402.1:p.Leu161Ser
ENST00000697695.1:n.1439_1441delinsAGC
XM_006722001.2:c.832_834delinsAGC XP_006722064.1:p.Leu278Ser
XM_006722001.4:c.832_834delinsAGC XP_006722064.1:p.Leu278Ser
XM_006722002.2:c.832_834delinsAGC XP_006722065.1:p.Leu278Ser
XM_006722002.4:c.832_834delinsAGC XP_006722065.1:p.Leu278Ser
XM_006722004.2:c.481_483delinsAGC XP_006722067.1:p.Leu161Ser
XM_006722004.3:c.481_483delinsAGC XP_006722067.1:p.Leu161Ser
XM_006722005.2:c.481_483delinsAGC XP_006722068.1:p.Leu161Ser
XM_006722005.3:c.481_483delinsAGC XP_006722068.1:p.Leu161Ser
XM_011525092.1:c.481_483delinsAGC XP_011523394.1:p.Leu161Ser
XM_011525092.2:c.481_483delinsAGC XP_011523394.1:p.Leu161Ser
XM_011525093.1:c.481_483delinsAGC XP_011523395.1:p.Leu161Ser
XM_011525093.2:c.481_483delinsAGC XP_011523395.1:p.Leu161Ser
XM_011525094.1:c.481_483delinsAGC XP_011523396.1:p.Leu161Ser
XM_011525094.2:c.481_483delinsAGC XP_011523396.1:p.Leu161Ser
XM_017024914.1:c.481_483delinsAGC XP_016880403.1:p.Leu161Ser
XM_017024915.1:c.481_483delinsAGC XP_016880404.1:p.Leu161Ser
XM_017024916.1:c.481_483delinsAGC XP_016880405.1:p.Leu161Ser
XM_017024917.1:c.481_483delinsAGC XP_016880406.1:p.Leu161Ser
XM_017024918.2:c.481_483delinsAGC XP_016880407.1:p.Leu161Ser
XM_017024919.1:c.481_483delinsAGC XP_016880408.1:p.Leu161Ser
XR_934513.1:n.1050_1052delinsAGC
XR_934513.3:n.1481_1483delinsAGC
XR_934514.1:n.1050_1052delinsAGC
XR_934514.3:n.1481_1483delinsAGC