Canonical Allele Identifier: CA3057243369
Community Standard Title: NM_058216.3(RAD51C):c.1029_1031del (p.Gln344del)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734120_58734122del , CM000679.2:g.58734120_58734122del GRCh38
NC_000017.10:g.56811481_56811483del , CM000679.1:g.56811481_56811483del GRCh37
NC_000017.9:g.54166480_54166482del NCBI36
NG_023199.1:g.46519_46521del , LRG_314:g.46519_46521del

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1029_1031del MANE Select NP_478123.1:p.Gln344del
ENST00000337432.9:c.1029_1031del MANE Select ENSP00000336701.4:p.Gln344del
NM_058216.2:c.1029_1031del NP_478123.1:p.Gln344del
NR_103872.1:n.933_935del
NR_103872.2:n.904_906del
ENST00000337432.8:c.1029_1031del ENSP00000336701.4:p.Gln344del
ENST00000413590.5:c.670_672del
ENST00000461271.6:c.*1561_*1563del ENSP00000464056.2:n.*1561_*1563del
ENST00000461706.1:n.216_218del
ENST00000475762.5:c.*1665_*1667del ENSP00000432421.1:n.*1665_*1667del
ENST00000482007.5:c.*457_*459del ENSP00000433332.1:n.*457_*459del
ENST00000487525.5:c.*605_*607del ENSP00000431637.1:n.*605_*607del
ENST00000578151.1:n.242_244del
ENST00000581221.5:n.544_546del
ENST00000584804.1:c.263_265del ENSP00000463658.1:p.Leu88del
ENST00000697680.1:c.*1993_*1995del ENSP00000513392.1:n.*1993_*1995del
ENST00000697681.1:c.*2190_*2192del ENSP00000513393.1:n.*2190_*2192del
ENST00000697683.1:c.*1965_*1967del ENSP00000513395.1:n.*1965_*1967del
ENST00000697685.1:c.*1726_*1728del ENSP00000513396.1:n.*1726_*1728del
ENST00000697686.1:c.800_802del ENSP00000513397.1:p.Leu267del
ENST00000697689.1:c.*1443_*1445del ENSP00000513398.1:n.*1443_*1445del
ENST00000697690.1:c.907_909del ENSP00000513399.1:p.Ser303del
ENST00000697691.1:c.*1001_*1003del ENSP00000513400.1:n.*1001_*1003del
ENST00000697692.1:c.*1041_*1043del ENSP00000513401.1:n.*1041_*1043del
ENST00000697694.1:c.678_680del ENSP00000513402.1:p.Gln227del
ENST00000697695.1:n.1636_1638del
XM_006722001.2:c.1032_1034del XP_006722064.1:p.Gln345del
XM_006722001.4:c.1032_1034del XP_006722064.1:p.Gln345del
XM_006722002.2:c.968_970del XP_006722065.1:p.Leu323del
XM_006722002.4:c.968_970del XP_006722065.1:p.Leu323del
XM_006722004.2:c.681_683del XP_006722067.1:p.Gln228del
XM_006722004.3:c.681_683del XP_006722067.1:p.Gln228del
XM_006722005.2:c.681_683del XP_006722068.1:p.Gln228del
XM_006722005.3:c.681_683del XP_006722068.1:p.Gln228del
XM_011525092.1:c.681_683del XP_011523394.1:p.Gln228del
XM_011525092.2:c.681_683del XP_011523394.1:p.Gln228del
XM_011525093.1:c.681_683del XP_011523395.1:p.Gln228del
XM_011525093.2:c.681_683del XP_011523395.1:p.Gln228del
XM_011525094.1:c.681_683del XP_011523396.1:p.Gln228del
XM_011525094.2:c.681_683del XP_011523396.1:p.Gln228del
XM_017024914.1:c.678_680del XP_016880403.1:p.Gln227del
XM_017024915.1:c.678_680del XP_016880404.1:p.Gln227del
XM_017024916.1:c.678_680del XP_016880405.1:p.Gln227del
XM_017024917.1:c.678_680del XP_016880406.1:p.Gln227del
XM_017024918.2:c.678_680del XP_016880407.1:p.Gln227del
XM_017024919.1:c.617_619del XP_016880408.1:p.Leu206del
XR_934513.1:n.1247_1249del
XR_934513.3:n.1678_1680del
XR_934514.1:n.1250_1252del
XR_934514.3:n.1681_1683del
XR_934886.1:n.149+3949_149+3951del
XR_934886.2:n.149+3949_149+3951del