Canonical Allele Identifier: CA3261179733
Community Standard Title: NM_058216.3(RAD51C):c.773_774delinsTG (p.Arg258Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709926_58709927delinsTG , CM000679.2:g.58709926_58709927delinsTG GRCh38
NC_000017.10:g.56787287_56787288delinsTG , CM000679.1:g.56787287_56787288delinsTG GRCh37
NC_000017.9:g.54142286_54142287delinsTG NCBI36
NG_023199.1:g.22325_22326delinsTG , LRG_314:g.22325_22326delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.773_774delinsTG MANE Select NP_478123.1:p.Arg258Leu
ENST00000337432.9:c.773_774delinsTG MANE Select ENSP00000336701.4:p.Arg258Leu
NM_058216.2:c.773_774delinsTG NP_478123.1:p.Arg258Leu
NR_103872.1:n.677_678delinsTG
NR_103872.2:n.648_649delinsTG
ENST00000337432.8:c.773_774delinsTG ENSP00000336701.4:p.Arg258Leu
ENST00000413590.5:c.411_412delinsTG
ENST00000461271.6:c.422_423delinsTG ENSP00000464056.2:p.Arg141Leu
ENST00000475762.5:c.*1476_*1477delinsTG ENSP00000432421.1:n.*1476_*1477delinsTG
ENST00000482007.5:c.*201_*202delinsTG ENSP00000433332.1:n.*201_*202delinsTG
ENST00000487525.5:c.*346_*347delinsTG ENSP00000431637.1:n.*346_*347delinsTG
ENST00000578151.1:n.108_109delinsTG
ENST00000581221.5:n.288_289delinsTG
ENST00000583539.5:c.773_774delinsTG ENSP00000463121.1:p.Arg258Leu
ENST00000584617.5:c.495_496delinsTG
ENST00000584804.1:c.68_69delinsTG ENSP00000463658.1:p.Arg23Leu
ENST00000697678.1:n.675_676delinsTG
ENST00000697679.1:n.1847_1848delinsTG
ENST00000697680.1:c.*1637_*1638delinsTG ENSP00000513392.1:n.*1637_*1638delinsTG
ENST00000697681.1:c.*1934_*1935delinsTG ENSP00000513393.1:n.*1934_*1935delinsTG
ENST00000697683.1:c.*1637_*1638delinsTG ENSP00000513395.1:n.*1637_*1638delinsTG
ENST00000697684.1:n.833_834delinsTG
ENST00000697685.1:c.*1470_*1471delinsTG ENSP00000513396.1:n.*1470_*1471delinsTG
ENST00000697686.1:c.422_423delinsTG ENSP00000513397.1:p.Arg141Leu
ENST00000697687.1:n.652_653delinsTG
ENST00000697688.1:n.819_820delinsTG
ENST00000697689.1:c.*1309_*1310delinsTG ENSP00000513398.1:n.*1309_*1310delinsTG
ENST00000697690.1:c.773_774delinsTG ENSP00000513399.1:p.Arg258Leu
ENST00000697691.1:c.*745_*746delinsTG ENSP00000513400.1:n.*745_*746delinsTG
ENST00000697692.1:c.*785_*786delinsTG ENSP00000513401.1:n.*785_*786delinsTG
ENST00000697694.1:c.422_423delinsTG ENSP00000513402.1:p.Arg141Leu
ENST00000697695.1:n.1380_1381delinsTG
XM_006722001.2:c.773_774delinsTG XP_006722064.1:p.Arg258Leu
XM_006722001.4:c.773_774delinsTG XP_006722064.1:p.Arg258Leu
XM_006722002.2:c.773_774delinsTG XP_006722065.1:p.Arg258Leu
XM_006722002.4:c.773_774delinsTG XP_006722065.1:p.Arg258Leu
XM_006722004.2:c.422_423delinsTG XP_006722067.1:p.Arg141Leu
XM_006722004.3:c.422_423delinsTG XP_006722067.1:p.Arg141Leu
XM_006722005.2:c.422_423delinsTG XP_006722068.1:p.Arg141Leu
XM_006722005.3:c.422_423delinsTG XP_006722068.1:p.Arg141Leu
XM_011525092.1:c.422_423delinsTG XP_011523394.1:p.Arg141Leu
XM_011525092.2:c.422_423delinsTG XP_011523394.1:p.Arg141Leu
XM_011525093.1:c.422_423delinsTG XP_011523395.1:p.Arg141Leu
XM_011525093.2:c.422_423delinsTG XP_011523395.1:p.Arg141Leu
XM_011525094.1:c.422_423delinsTG XP_011523396.1:p.Arg141Leu
XM_011525094.2:c.422_423delinsTG XP_011523396.1:p.Arg141Leu
XM_017024914.1:c.422_423delinsTG XP_016880403.1:p.Arg141Leu
XM_017024915.1:c.422_423delinsTG XP_016880404.1:p.Arg141Leu
XM_017024916.1:c.422_423delinsTG XP_016880405.1:p.Arg141Leu
XM_017024917.1:c.422_423delinsTG XP_016880406.1:p.Arg141Leu
XM_017024918.2:c.422_423delinsTG XP_016880407.1:p.Arg141Leu
XM_017024919.1:c.422_423delinsTG XP_016880408.1:p.Arg141Leu
XR_934513.1:n.991_992delinsTG
XR_934513.3:n.1422_1423delinsTG
XR_934514.1:n.991_992delinsTG
XR_934514.3:n.1422_1423delinsTG