Canonical Allele Identifier: CA3057243382
Community Standard Title: NM_058216.3(RAD51C):c.1071_1073del (p.Gln358del)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734162_58734164del , CM000679.2:g.58734162_58734164del GRCh38
NC_000017.10:g.56811523_56811525del , CM000679.1:g.56811523_56811525del GRCh37
NC_000017.9:g.54166522_54166524del NCBI36
NG_023199.1:g.46561_46563del , LRG_314:g.46561_46563del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1071_1073del MANE Select NP_478123.1:p.Gln358del
ENST00000337432.9:c.1071_1073del MANE Select ENSP00000336701.4:p.Gln358del
NM_058216.2:c.1071_1073del NP_478123.1:p.Gln358del
NR_103872.1:n.975_977del
NR_103872.2:n.946_948del
ENST00000337432.8:c.1071_1073del ENSP00000336701.4:p.Gln358del
ENST00000413590.5:c.712_714del
ENST00000461271.6:c.*1603_*1605del ENSP00000464056.2:n.*1603_*1605del
ENST00000461706.1:n.258_260del
ENST00000475762.5:c.*1707_*1709del ENSP00000432421.1:n.*1707_*1709del
ENST00000482007.5:c.*499_*501del ENSP00000433332.1:n.*499_*501del
ENST00000487525.5:c.*647_*649del ENSP00000431637.1:n.*647_*649del
ENST00000578151.1:n.284_286del
ENST00000581221.5:n.586_588del
ENST00000584804.1:c.305_307del ENSP00000463658.1:p.Cys102Ter
ENST00000697680.1:c.*2035_*2037del ENSP00000513392.1:n.*2035_*2037del
ENST00000697681.1:c.*2232_*2234del ENSP00000513393.1:n.*2232_*2234del
ENST00000697683.1:c.*2007_*2009del ENSP00000513395.1:n.*2007_*2009del
ENST00000697685.1:c.*1768_*1770del ENSP00000513396.1:n.*1768_*1770del
ENST00000697686.1:c.842_844del ENSP00000513397.1:p.Cys281Ter
ENST00000697689.1:c.*1485_*1487del ENSP00000513398.1:n.*1485_*1487del
ENST00000697690.1:c.*31_*33del ENSP00000513399.1:n.*31_*33del
ENST00000697691.1:c.*1043_*1045del ENSP00000513400.1:n.*1043_*1045del
ENST00000697692.1:c.*1083_*1085del ENSP00000513401.1:n.*1083_*1085del
ENST00000697694.1:c.720_722del ENSP00000513402.1:p.Gln241del
ENST00000697695.1:n.1678_1680del
XM_006722001.2:c.1074_1076del XP_006722064.1:p.Gln359del
XM_006722001.4:c.1074_1076del XP_006722064.1:p.Gln359del
XM_006722002.2:c.1010_1012del XP_006722065.1:p.Cys337Ter
XM_006722002.4:c.1010_1012del XP_006722065.1:p.Cys337Ter
XM_006722004.2:c.723_725del XP_006722067.1:p.Gln242del
XM_006722004.3:c.723_725del XP_006722067.1:p.Gln242del
XM_006722005.2:c.723_725del XP_006722068.1:p.Gln242del
XM_006722005.3:c.723_725del XP_006722068.1:p.Gln242del
XM_011525092.1:c.723_725del XP_011523394.1:p.Gln242del
XM_011525092.2:c.723_725del XP_011523394.1:p.Gln242del
XM_011525093.1:c.723_725del XP_011523395.1:p.Gln242del
XM_011525093.2:c.723_725del XP_011523395.1:p.Gln242del
XM_011525094.1:c.723_725del XP_011523396.1:p.Gln242del
XM_011525094.2:c.723_725del XP_011523396.1:p.Gln242del
XM_017024914.1:c.720_722del XP_016880403.1:p.Gln241del
XM_017024915.1:c.720_722del XP_016880404.1:p.Gln241del
XM_017024916.1:c.720_722del XP_016880405.1:p.Gln241del
XM_017024917.1:c.720_722del XP_016880406.1:p.Gln241del
XM_017024918.2:c.720_722del XP_016880407.1:p.Gln241del
XM_017024919.1:c.659_661del XP_016880408.1:p.Cys220Ter
XR_934513.1:n.1289_1291del
XR_934513.3:n.1720_1722del
XR_934514.1:n.1292_1294del
XR_934514.3:n.1723_1725del
XR_934886.1:n.149+3907_149+3909del
XR_934886.2:n.149+3907_149+3909del