Canonical Allele Identifier: CA3261178791
Community Standard Title: NM_058216.3(RAD51C):c.865_866delinsCG (p.Lys289Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720773_58720774delinsCG , CM000679.2:g.58720773_58720774delinsCG GRCh38
NC_000017.10:g.56798134_56798135delinsCG , CM000679.1:g.56798134_56798135delinsCG GRCh37
NC_000017.9:g.54153133_54153134delinsCG NCBI36
NG_023199.1:g.33172_33173delinsCG , LRG_314:g.33172_33173delinsCG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.865_866delinsCG MANE Select NP_478123.1:p.Lys289Arg
ENST00000337432.9:c.865_866delinsCG MANE Select ENSP00000336701.4:p.Lys289Arg
NM_058216.2:c.865_866delinsCG NP_478123.1:p.Lys289Arg
NR_103872.1:n.769_770delinsCG
NR_103872.2:n.740_741delinsCG
ENST00000337432.8:c.865_866delinsCG ENSP00000336701.4:p.Lys289Arg
ENST00000413590.5:c.503_504delinsCG
ENST00000461271.6:c.514_515delinsCG ENSP00000464056.2:p.Lys172Arg
ENST00000475762.5:c.*1541-3267_*1541-3266delinsCG ENSP00000432421.1:n.*1541-3267_*1541-3266delinsCG
ENST00000482007.5:c.*293_*294delinsCG ENSP00000433332.1:n.*293_*294delinsCG
ENST00000487525.5:c.*438_*439delinsCG ENSP00000431637.1:n.*438_*439delinsCG
ENST00000578151.1:n.200_201delinsCG
ENST00000581221.5:n.380_381delinsCG
ENST00000583539.5:c.865_866delinsCG ENSP00000463121.1:p.Lys289Arg
ENST00000584617.5:c.587_588delinsCG
ENST00000584804.1:c.160_161delinsCG ENSP00000463658.1:p.Lys54Arg
ENST00000697678.1:n.767_768delinsCG
ENST00000697679.1:n.1939_1940delinsCG
ENST00000697680.1:c.*1829_*1830delinsCG ENSP00000513392.1:n.*1829_*1830delinsCG
ENST00000697681.1:c.*2026_*2027delinsCG ENSP00000513393.1:n.*2026_*2027delinsCG
ENST00000697683.1:c.*1729_*1730delinsCG ENSP00000513395.1:n.*1729_*1730delinsCG
ENST00000697684.1:n.925_926delinsCG
ENST00000697685.1:c.*1562_*1563delinsCG ENSP00000513396.1:n.*1562_*1563delinsCG
ENST00000697686.1:c.514_515delinsCG ENSP00000513397.1:p.Lys172Arg
ENST00000697687.1:n.744_745delinsCG
ENST00000697688.1:n.911_912delinsCG
ENST00000697689.1:c.*1401_*1402delinsCG ENSP00000513398.1:n.*1401_*1402delinsCG
ENST00000697690.1:c.865_866delinsCG ENSP00000513399.1:p.Lys289Arg
ENST00000697691.1:c.*837_*838delinsCG ENSP00000513400.1:n.*837_*838delinsCG
ENST00000697692.1:c.*877_*878delinsCG ENSP00000513401.1:n.*877_*878delinsCG
ENST00000697694.1:c.514_515delinsCG ENSP00000513402.1:p.Lys172Arg
ENST00000697695.1:n.1472_1473delinsCG
XM_006722001.2:c.865_866delinsCG XP_006722064.1:p.Lys289Arg
XM_006722001.4:c.865_866delinsCG XP_006722064.1:p.Lys289Arg
XM_006722002.2:c.865_866delinsCG XP_006722065.1:p.Lys289Arg
XM_006722002.4:c.865_866delinsCG XP_006722065.1:p.Lys289Arg
XM_006722004.2:c.514_515delinsCG XP_006722067.1:p.Lys172Arg
XM_006722004.3:c.514_515delinsCG XP_006722067.1:p.Lys172Arg
XM_006722005.2:c.514_515delinsCG XP_006722068.1:p.Lys172Arg
XM_006722005.3:c.514_515delinsCG XP_006722068.1:p.Lys172Arg
XM_011525092.1:c.514_515delinsCG XP_011523394.1:p.Lys172Arg
XM_011525092.2:c.514_515delinsCG XP_011523394.1:p.Lys172Arg
XM_011525093.1:c.514_515delinsCG XP_011523395.1:p.Lys172Arg
XM_011525093.2:c.514_515delinsCG XP_011523395.1:p.Lys172Arg
XM_011525094.1:c.514_515delinsCG XP_011523396.1:p.Lys172Arg
XM_011525094.2:c.514_515delinsCG XP_011523396.1:p.Lys172Arg
XM_017024914.1:c.514_515delinsCG XP_016880403.1:p.Lys172Arg
XM_017024915.1:c.514_515delinsCG XP_016880404.1:p.Lys172Arg
XM_017024916.1:c.514_515delinsCG XP_016880405.1:p.Lys172Arg
XM_017024917.1:c.514_515delinsCG XP_016880406.1:p.Lys172Arg
XM_017024918.2:c.514_515delinsCG XP_016880407.1:p.Lys172Arg
XM_017024919.1:c.514_515delinsCG XP_016880408.1:p.Lys172Arg
XR_934513.1:n.1083_1084delinsCG
XR_934513.3:n.1514_1515delinsCG
XR_934514.1:n.1083_1084delinsCG
XR_934514.3:n.1514_1515delinsCG