Canonical Allele Identifier: CA3261179284
Community Standard Title: NM_058216.3(RAD51C):c.620_621delinsGG (p.His207Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703244_58703245delinsGG , CM000679.2:g.58703244_58703245delinsGG GRCh38
NC_000017.10:g.56780605_56780606delinsGG , CM000679.1:g.56780605_56780606delinsGG GRCh37
NC_000017.9:g.54135604_54135605delinsGG NCBI36
NG_023199.1:g.15643_15644delinsGG , LRG_314:g.15643_15644delinsGG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.620_621delinsGG MANE Select NP_478123.1:p.His207Arg
ENST00000337432.9:c.620_621delinsGG MANE Select ENSP00000336701.4:p.His207Arg
NM_058216.2:c.620_621delinsGG NP_478123.1:p.His207Arg
NR_103872.1:n.524_525delinsGG
NR_103872.2:n.495_496delinsGG
ENST00000337432.8:c.620_621delinsGG ENSP00000336701.4:p.His207Arg
ENST00000413590.5:c.258_259delinsGG
ENST00000425173.5:c.416_417delinsGG ENSP00000407282.1:p.His139Arg
ENST00000461271.5:c.269_270delinsGG ENSP00000464056.1:p.His90Arg
ENST00000461271.6:c.269_270delinsGG ENSP00000464056.2:p.His90Arg
ENST00000475762.5:c.*1323_*1324delinsGG ENSP00000432421.1:n.*1323_*1324delinsGG
ENST00000482007.5:c.*48_*49delinsGG ENSP00000433332.1:n.*48_*49delinsGG
ENST00000487525.5:c.*48_*49delinsGG ENSP00000431637.1:n.*48_*49delinsGG
ENST00000487921.5:n.532_533delinsGG
ENST00000583539.5:c.620_621delinsGG ENSP00000463121.1:p.His207Arg
ENST00000584617.5:c.342_343delinsGG
ENST00000697677.1:n.1701_1702delinsGG
ENST00000697678.1:n.522_523delinsGG
ENST00000697679.1:n.1694_1695delinsGG
ENST00000697680.1:c.*1484_*1485delinsGG ENSP00000513392.1:n.*1484_*1485delinsGG
ENST00000697681.1:c.*1636_*1637delinsGG ENSP00000513393.1:n.*1636_*1637delinsGG
ENST00000697683.1:c.*1484_*1485delinsGG ENSP00000513395.1:n.*1484_*1485delinsGG
ENST00000697684.1:n.680_681delinsGG
ENST00000697685.1:c.*1317_*1318delinsGG ENSP00000513396.1:n.*1317_*1318delinsGG
ENST00000697686.1:c.269_270delinsGG ENSP00000513397.1:p.His90Arg
ENST00000697687.1:n.499_500delinsGG
ENST00000697688.1:n.666_667delinsGG
ENST00000697689.1:c.*1156_*1157delinsGG ENSP00000513398.1:n.*1156_*1157delinsGG
ENST00000697690.1:c.620_621delinsGG ENSP00000513399.1:p.His207Arg
ENST00000697691.1:c.*592_*593delinsGG ENSP00000513400.1:n.*592_*593delinsGG
ENST00000697692.1:c.*632_*633delinsGG ENSP00000513401.1:n.*632_*633delinsGG
ENST00000697694.1:c.269_270delinsGG ENSP00000513402.1:p.His90Arg
ENST00000697695.1:n.1227_1228delinsGG
XM_006722001.2:c.620_621delinsGG XP_006722064.1:p.His207Arg
XM_006722001.4:c.620_621delinsGG XP_006722064.1:p.His207Arg
XM_006722002.2:c.620_621delinsGG XP_006722065.1:p.His207Arg
XM_006722002.4:c.620_621delinsGG XP_006722065.1:p.His207Arg
XM_006722004.2:c.269_270delinsGG XP_006722067.1:p.His90Arg
XM_006722004.3:c.269_270delinsGG XP_006722067.1:p.His90Arg
XM_006722005.2:c.269_270delinsGG XP_006722068.1:p.His90Arg
XM_006722005.3:c.269_270delinsGG XP_006722068.1:p.His90Arg
XM_011525092.1:c.269_270delinsGG XP_011523394.1:p.His90Arg
XM_011525092.2:c.269_270delinsGG XP_011523394.1:p.His90Arg
XM_011525093.1:c.269_270delinsGG XP_011523395.1:p.His90Arg
XM_011525093.2:c.269_270delinsGG XP_011523395.1:p.His90Arg
XM_011525094.1:c.269_270delinsGG XP_011523396.1:p.His90Arg
XM_011525094.2:c.269_270delinsGG XP_011523396.1:p.His90Arg
XM_017024914.1:c.269_270delinsGG XP_016880403.1:p.His90Arg
XM_017024915.1:c.269_270delinsGG XP_016880404.1:p.His90Arg
XM_017024916.1:c.269_270delinsGG XP_016880405.1:p.His90Arg
XM_017024917.1:c.269_270delinsGG XP_016880406.1:p.His90Arg
XM_017024918.2:c.269_270delinsGG XP_016880407.1:p.His90Arg
XM_017024919.1:c.269_270delinsGG XP_016880408.1:p.His90Arg
XR_934513.1:n.693_694delinsGG
XR_934513.3:n.1124_1125delinsGG
XR_934514.1:n.693_694delinsGG
XR_934514.3:n.1124_1125delinsGG