Canonical Allele Identifier: CA3261180174
Community Standard Title: NM_058216.3(RAD51C):c.1060_1062del (p.Ala354del)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734151_58734153del , CM000679.2:g.58734151_58734153del GRCh38
NC_000017.10:g.56811512_56811514del , CM000679.1:g.56811512_56811514del GRCh37
NC_000017.9:g.54166511_54166513del NCBI36
NG_023199.1:g.46550_46552del , LRG_314:g.46550_46552del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1060_1062del MANE Select NP_478123.1:p.Ala354del
ENST00000337432.9:c.1060_1062del MANE Select ENSP00000336701.4:p.Ala354del
NM_058216.2:c.1060_1062del NP_478123.1:p.Ala354del
NR_103872.1:n.964_966del
NR_103872.2:n.935_937del
ENST00000337432.8:c.1060_1062del ENSP00000336701.4:p.Ala354del
ENST00000413590.5:c.701_703del
ENST00000461271.6:c.*1592_*1594del ENSP00000464056.2:n.*1592_*1594del
ENST00000461706.1:n.247_249del
ENST00000475762.5:c.*1696_*1698del ENSP00000432421.1:n.*1696_*1698del
ENST00000482007.5:c.*488_*490del ENSP00000433332.1:n.*488_*490del
ENST00000487525.5:c.*636_*638del ENSP00000431637.1:n.*636_*638del
ENST00000578151.1:n.273_275del
ENST00000581221.5:n.575_577del
ENST00000584804.1:c.294_296del ENSP00000463658.1:p.His99del
ENST00000697680.1:c.*2024_*2026del ENSP00000513392.1:n.*2024_*2026del
ENST00000697681.1:c.*2221_*2223del ENSP00000513393.1:n.*2221_*2223del
ENST00000697683.1:c.*1996_*1998del ENSP00000513395.1:n.*1996_*1998del
ENST00000697685.1:c.*1757_*1759del ENSP00000513396.1:n.*1757_*1759del
ENST00000697686.1:c.831_833del ENSP00000513397.1:p.His278del
ENST00000697689.1:c.*1474_*1476del ENSP00000513398.1:n.*1474_*1476del
ENST00000697690.1:c.*20_*22del ENSP00000513399.1:n.*20_*22del
ENST00000697691.1:c.*1032_*1034del ENSP00000513400.1:n.*1032_*1034del
ENST00000697692.1:c.*1072_*1074del ENSP00000513401.1:n.*1072_*1074del
ENST00000697694.1:c.709_711del ENSP00000513402.1:p.Ala237del
ENST00000697695.1:n.1667_1669del
XM_006722001.2:c.1063_1065del XP_006722064.1:p.Ala355del
XM_006722001.4:c.1063_1065del XP_006722064.1:p.Ala355del
XM_006722002.2:c.999_1001del XP_006722065.1:p.His334del
XM_006722002.4:c.999_1001del XP_006722065.1:p.His334del
XM_006722004.2:c.712_714del XP_006722067.1:p.Ala238del
XM_006722004.3:c.712_714del XP_006722067.1:p.Ala238del
XM_006722005.2:c.712_714del XP_006722068.1:p.Ala238del
XM_006722005.3:c.712_714del XP_006722068.1:p.Ala238del
XM_011525092.1:c.712_714del XP_011523394.1:p.Ala238del
XM_011525092.2:c.712_714del XP_011523394.1:p.Ala238del
XM_011525093.1:c.712_714del XP_011523395.1:p.Ala238del
XM_011525093.2:c.712_714del XP_011523395.1:p.Ala238del
XM_011525094.1:c.712_714del XP_011523396.1:p.Ala238del
XM_011525094.2:c.712_714del XP_011523396.1:p.Ala238del
XM_017024914.1:c.709_711del XP_016880403.1:p.Ala237del
XM_017024915.1:c.709_711del XP_016880404.1:p.Ala237del
XM_017024916.1:c.709_711del XP_016880405.1:p.Ala237del
XM_017024917.1:c.709_711del XP_016880406.1:p.Ala237del
XM_017024918.2:c.709_711del XP_016880407.1:p.Ala237del
XM_017024919.1:c.648_650del XP_016880408.1:p.His217del
XR_934513.1:n.1278_1280del
XR_934513.3:n.1709_1711del
XR_934514.1:n.1281_1283del
XR_934514.3:n.1712_1714del
XR_934886.1:n.149+3918_149+3920del
XR_934886.2:n.149+3918_149+3920del