Canonical Allele Identifier: CA3057243487
Community Standard Title: NM_058216.3(RAD51C):c.1029_1031delinsAAG (p.Gln344Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734120_58734122delinsAAG , CM000679.2:g.58734120_58734122delinsAAG GRCh38
NC_000017.10:g.56811481_56811483delinsAAG , CM000679.1:g.56811481_56811483delinsAAG GRCh37
NC_000017.9:g.54166480_54166482delinsAAG NCBI36
NG_023199.1:g.46519_46521delinsAAG , LRG_314:g.46519_46521delinsAAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1029_1031delinsAAG MANE Select NP_478123.1:p.Gln344Arg
ENST00000337432.9:c.1029_1031delinsAAG MANE Select ENSP00000336701.4:p.Gln344Arg
NM_058216.2:c.1029_1031delinsAAG NP_478123.1:p.Gln344Arg
NR_103872.1:n.933_935delinsAAG
NR_103872.2:n.904_906delinsAAG
ENST00000337432.8:c.1029_1031delinsAAG ENSP00000336701.4:p.Gln344Arg
ENST00000413590.5:c.670_672delinsAAG
ENST00000461271.6:c.*1561_*1563delinsAAG ENSP00000464056.2:n.*1561_*1563delinsAAG
ENST00000461706.1:n.216_218delinsAAG
ENST00000475762.5:c.*1665_*1667delinsAAG ENSP00000432421.1:n.*1665_*1667delinsAAG
ENST00000482007.5:c.*457_*459delinsAAG ENSP00000433332.1:n.*457_*459delinsAAG
ENST00000487525.5:c.*605_*607delinsAAG ENSP00000431637.1:n.*605_*607delinsAAG
ENST00000578151.1:n.242_244delinsAAG
ENST00000581221.5:n.544_546delinsAAG
ENST00000584804.1:c.263_265delinsAAG ENSP00000463658.1:p.Leu88_Arg89delinsGlnGly
ENST00000697680.1:c.*1993_*1995delinsAAG ENSP00000513392.1:n.*1993_*1995delinsAAG
ENST00000697681.1:c.*2190_*2192delinsAAG ENSP00000513393.1:n.*2190_*2192delinsAAG
ENST00000697683.1:c.*1965_*1967delinsAAG ENSP00000513395.1:n.*1965_*1967delinsAAG
ENST00000697685.1:c.*1726_*1728delinsAAG ENSP00000513396.1:n.*1726_*1728delinsAAG
ENST00000697686.1:c.800_802delinsAAG ENSP00000513397.1:p.Leu267_Arg268delinsGlnGly
ENST00000697689.1:c.*1443_*1445delinsAAG ENSP00000513398.1:n.*1443_*1445delinsAAG
ENST00000697690.1:c.907_909delinsAAG ENSP00000513399.1:p.Ser303Lys
ENST00000697691.1:c.*1001_*1003delinsAAG ENSP00000513400.1:n.*1001_*1003delinsAAG
ENST00000697692.1:c.*1041_*1043delinsAAG ENSP00000513401.1:n.*1041_*1043delinsAAG
ENST00000697694.1:c.678_680delinsAAG ENSP00000513402.1:p.Gln227Arg
ENST00000697695.1:n.1636_1638delinsAAG
XM_006722001.2:c.1032_1034delinsAAG XP_006722064.1:p.Gln345Arg
XM_006722001.4:c.1032_1034delinsAAG XP_006722064.1:p.Gln345Arg
XM_006722002.2:c.968_970delinsAAG XP_006722065.1:p.Leu323_Arg324delinsGlnGly
XM_006722002.4:c.968_970delinsAAG XP_006722065.1:p.Leu323_Arg324delinsGlnGly
XM_006722004.2:c.681_683delinsAAG XP_006722067.1:p.Gln228Arg
XM_006722004.3:c.681_683delinsAAG XP_006722067.1:p.Gln228Arg
XM_006722005.2:c.681_683delinsAAG XP_006722068.1:p.Gln228Arg
XM_006722005.3:c.681_683delinsAAG XP_006722068.1:p.Gln228Arg
XM_011525092.1:c.681_683delinsAAG XP_011523394.1:p.Gln228Arg
XM_011525092.2:c.681_683delinsAAG XP_011523394.1:p.Gln228Arg
XM_011525093.1:c.681_683delinsAAG XP_011523395.1:p.Gln228Arg
XM_011525093.2:c.681_683delinsAAG XP_011523395.1:p.Gln228Arg
XM_011525094.1:c.681_683delinsAAG XP_011523396.1:p.Gln228Arg
XM_011525094.2:c.681_683delinsAAG XP_011523396.1:p.Gln228Arg
XM_017024914.1:c.678_680delinsAAG XP_016880403.1:p.Gln227Arg
XM_017024915.1:c.678_680delinsAAG XP_016880404.1:p.Gln227Arg
XM_017024916.1:c.678_680delinsAAG XP_016880405.1:p.Gln227Arg
XM_017024917.1:c.678_680delinsAAG XP_016880406.1:p.Gln227Arg
XM_017024918.2:c.678_680delinsAAG XP_016880407.1:p.Gln227Arg
XM_017024919.1:c.617_619delinsAAG XP_016880408.1:p.Leu206_Arg207delinsGlnGly
XR_934513.1:n.1247_1249delinsAAG
XR_934513.3:n.1678_1680delinsAAG
XR_934514.1:n.1250_1252delinsAAG
XR_934514.3:n.1681_1683delinsAAG
XR_934886.1:n.149+3949_149+3951delinsCTT
XR_934886.2:n.149+3949_149+3951delinsCTT