Canonical Allele Identifier: CA3057243488
Community Standard Title: NM_058216.3(RAD51C):c.1029_1031delinsGAG (p.Gln344Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734120_58734122delinsGAG , CM000679.2:g.58734120_58734122delinsGAG GRCh38
NC_000017.10:g.56811481_56811483delinsGAG , CM000679.1:g.56811481_56811483delinsGAG GRCh37
NC_000017.9:g.54166480_54166482delinsGAG NCBI36
NG_023199.1:g.46519_46521delinsGAG , LRG_314:g.46519_46521delinsGAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1029_1031delinsGAG MANE Select NP_478123.1:p.Gln344Arg
ENST00000337432.9:c.1029_1031delinsGAG MANE Select ENSP00000336701.4:p.Gln344Arg
NM_058216.2:c.1029_1031delinsGAG NP_478123.1:p.Gln344Arg
NR_103872.1:n.933_935delinsGAG
NR_103872.2:n.904_906delinsGAG
ENST00000337432.8:c.1029_1031delinsGAG ENSP00000336701.4:p.Gln344Arg
ENST00000413590.5:c.670_672delinsGAG
ENST00000461271.6:c.*1561_*1563delinsGAG ENSP00000464056.2:n.*1561_*1563delinsGAG
ENST00000461706.1:n.216_218delinsGAG
ENST00000475762.5:c.*1665_*1667delinsGAG ENSP00000432421.1:n.*1665_*1667delinsGAG
ENST00000482007.5:c.*457_*459delinsGAG ENSP00000433332.1:n.*457_*459delinsGAG
ENST00000487525.5:c.*605_*607delinsGAG ENSP00000431637.1:n.*605_*607delinsGAG
ENST00000578151.1:n.242_244delinsGAG
ENST00000581221.5:n.544_546delinsGAG
ENST00000584804.1:c.263_265delinsGAG ENSP00000463658.1:p.Leu88_Arg89delinsArgGly
ENST00000697680.1:c.*1993_*1995delinsGAG ENSP00000513392.1:n.*1993_*1995delinsGAG
ENST00000697681.1:c.*2190_*2192delinsGAG ENSP00000513393.1:n.*2190_*2192delinsGAG
ENST00000697683.1:c.*1965_*1967delinsGAG ENSP00000513395.1:n.*1965_*1967delinsGAG
ENST00000697685.1:c.*1726_*1728delinsGAG ENSP00000513396.1:n.*1726_*1728delinsGAG
ENST00000697686.1:c.800_802delinsGAG ENSP00000513397.1:p.Leu267_Arg268delinsArgGly
ENST00000697689.1:c.*1443_*1445delinsGAG ENSP00000513398.1:n.*1443_*1445delinsGAG
ENST00000697690.1:c.907_909delinsGAG ENSP00000513399.1:p.Ser303Glu
ENST00000697691.1:c.*1001_*1003delinsGAG ENSP00000513400.1:n.*1001_*1003delinsGAG
ENST00000697692.1:c.*1041_*1043delinsGAG ENSP00000513401.1:n.*1041_*1043delinsGAG
ENST00000697694.1:c.678_680delinsGAG ENSP00000513402.1:p.Gln227Arg
ENST00000697695.1:n.1636_1638delinsGAG
XM_006722001.2:c.1032_1034delinsGAG XP_006722064.1:p.Gln345Arg
XM_006722001.4:c.1032_1034delinsGAG XP_006722064.1:p.Gln345Arg
XM_006722002.2:c.968_970delinsGAG XP_006722065.1:p.Leu323_Arg324delinsArgGly
XM_006722002.4:c.968_970delinsGAG XP_006722065.1:p.Leu323_Arg324delinsArgGly
XM_006722004.2:c.681_683delinsGAG XP_006722067.1:p.Gln228Arg
XM_006722004.3:c.681_683delinsGAG XP_006722067.1:p.Gln228Arg
XM_006722005.2:c.681_683delinsGAG XP_006722068.1:p.Gln228Arg
XM_006722005.3:c.681_683delinsGAG XP_006722068.1:p.Gln228Arg
XM_011525092.1:c.681_683delinsGAG XP_011523394.1:p.Gln228Arg
XM_011525092.2:c.681_683delinsGAG XP_011523394.1:p.Gln228Arg
XM_011525093.1:c.681_683delinsGAG XP_011523395.1:p.Gln228Arg
XM_011525093.2:c.681_683delinsGAG XP_011523395.1:p.Gln228Arg
XM_011525094.1:c.681_683delinsGAG XP_011523396.1:p.Gln228Arg
XM_011525094.2:c.681_683delinsGAG XP_011523396.1:p.Gln228Arg
XM_017024914.1:c.678_680delinsGAG XP_016880403.1:p.Gln227Arg
XM_017024915.1:c.678_680delinsGAG XP_016880404.1:p.Gln227Arg
XM_017024916.1:c.678_680delinsGAG XP_016880405.1:p.Gln227Arg
XM_017024917.1:c.678_680delinsGAG XP_016880406.1:p.Gln227Arg
XM_017024918.2:c.678_680delinsGAG XP_016880407.1:p.Gln227Arg
XM_017024919.1:c.617_619delinsGAG XP_016880408.1:p.Leu206_Arg207delinsArgGly
XR_934513.1:n.1247_1249delinsGAG
XR_934513.3:n.1678_1680delinsGAG
XR_934514.1:n.1250_1252delinsGAG
XR_934514.3:n.1681_1683delinsGAG
XR_934886.1:n.149+3949_149+3951delinsCTC
XR_934886.2:n.149+3949_149+3951delinsCTC