Canonical Allele Identifier: CA3057243021
Community Standard Title: NM_058216.3(RAD51C):c.864_866delinsCAG (p.Lys289Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720772_58720774delinsCAG , CM000679.2:g.58720772_58720774delinsCAG GRCh38
NC_000017.10:g.56798133_56798135delinsCAG , CM000679.1:g.56798133_56798135delinsCAG GRCh37
NC_000017.9:g.54153132_54153134delinsCAG NCBI36
NG_023199.1:g.33171_33173delinsCAG , LRG_314:g.33171_33173delinsCAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.864_866delinsCAG MANE Select NP_478123.1:p.Lys289Arg
ENST00000337432.9:c.864_866delinsCAG MANE Select ENSP00000336701.4:p.Lys289Arg
NM_058216.2:c.864_866delinsCAG NP_478123.1:p.Lys289Arg
NR_103872.1:n.768_770delinsCAG
NR_103872.2:n.739_741delinsCAG
ENST00000337432.8:c.864_866delinsCAG ENSP00000336701.4:p.Lys289Arg
ENST00000413590.5:c.502_504delinsCAG
ENST00000461271.6:c.513_515delinsCAG ENSP00000464056.2:p.Lys172Arg
ENST00000475762.5:c.*1541-3268_*1541-3266delinsCAG ENSP00000432421.1:n.*1541-3268_*1541-3266delinsCAG
ENST00000482007.5:c.*292_*294delinsCAG ENSP00000433332.1:n.*292_*294delinsCAG
ENST00000487525.5:c.*437_*439delinsCAG ENSP00000431637.1:n.*437_*439delinsCAG
ENST00000578151.1:n.199_201delinsCAG
ENST00000581221.5:n.379_381delinsCAG
ENST00000583539.5:c.864_866delinsCAG ENSP00000463121.1:p.Lys289Arg
ENST00000584617.5:c.586_588delinsCAG
ENST00000584804.1:c.159_161delinsCAG ENSP00000463658.1:p.Lys54Arg
ENST00000697678.1:n.766_768delinsCAG
ENST00000697679.1:n.1938_1940delinsCAG
ENST00000697680.1:c.*1828_*1830delinsCAG ENSP00000513392.1:n.*1828_*1830delinsCAG
ENST00000697681.1:c.*2025_*2027delinsCAG ENSP00000513393.1:n.*2025_*2027delinsCAG
ENST00000697683.1:c.*1728_*1730delinsCAG ENSP00000513395.1:n.*1728_*1730delinsCAG
ENST00000697684.1:n.924_926delinsCAG
ENST00000697685.1:c.*1561_*1563delinsCAG ENSP00000513396.1:n.*1561_*1563delinsCAG
ENST00000697686.1:c.513_515delinsCAG ENSP00000513397.1:p.Lys172Arg
ENST00000697687.1:n.743_745delinsCAG
ENST00000697688.1:n.910_912delinsCAG
ENST00000697689.1:c.*1400_*1402delinsCAG ENSP00000513398.1:n.*1400_*1402delinsCAG
ENST00000697690.1:c.864_866delinsCAG ENSP00000513399.1:p.Lys289Arg
ENST00000697691.1:c.*836_*838delinsCAG ENSP00000513400.1:n.*836_*838delinsCAG
ENST00000697692.1:c.*876_*878delinsCAG ENSP00000513401.1:n.*876_*878delinsCAG
ENST00000697694.1:c.513_515delinsCAG ENSP00000513402.1:p.Lys172Arg
ENST00000697695.1:n.1471_1473delinsCAG
XM_006722001.2:c.864_866delinsCAG XP_006722064.1:p.Lys289Arg
XM_006722001.4:c.864_866delinsCAG XP_006722064.1:p.Lys289Arg
XM_006722002.2:c.864_866delinsCAG XP_006722065.1:p.Lys289Arg
XM_006722002.4:c.864_866delinsCAG XP_006722065.1:p.Lys289Arg
XM_006722004.2:c.513_515delinsCAG XP_006722067.1:p.Lys172Arg
XM_006722004.3:c.513_515delinsCAG XP_006722067.1:p.Lys172Arg
XM_006722005.2:c.513_515delinsCAG XP_006722068.1:p.Lys172Arg
XM_006722005.3:c.513_515delinsCAG XP_006722068.1:p.Lys172Arg
XM_011525092.1:c.513_515delinsCAG XP_011523394.1:p.Lys172Arg
XM_011525092.2:c.513_515delinsCAG XP_011523394.1:p.Lys172Arg
XM_011525093.1:c.513_515delinsCAG XP_011523395.1:p.Lys172Arg
XM_011525093.2:c.513_515delinsCAG XP_011523395.1:p.Lys172Arg
XM_011525094.1:c.513_515delinsCAG XP_011523396.1:p.Lys172Arg
XM_011525094.2:c.513_515delinsCAG XP_011523396.1:p.Lys172Arg
XM_017024914.1:c.513_515delinsCAG XP_016880403.1:p.Lys172Arg
XM_017024915.1:c.513_515delinsCAG XP_016880404.1:p.Lys172Arg
XM_017024916.1:c.513_515delinsCAG XP_016880405.1:p.Lys172Arg
XM_017024917.1:c.513_515delinsCAG XP_016880406.1:p.Lys172Arg
XM_017024918.2:c.513_515delinsCAG XP_016880407.1:p.Lys172Arg
XM_017024919.1:c.513_515delinsCAG XP_016880408.1:p.Lys172Arg
XR_934513.1:n.1082_1084delinsCAG
XR_934513.3:n.1513_1515delinsCAG
XR_934514.1:n.1082_1084delinsCAG
XR_934514.3:n.1513_1515delinsCAG