Canonical Allele Identifier: CA2267819466
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703244_58703248delinsATATT , CM000679.2:g.58703244_58703248delinsATATT GRCh38
NC_000017.10:g.56780605_56780609delinsATATT , CM000679.1:g.56780605_56780609delinsATATT GRCh37
NC_000017.9:g.54135604_54135608delinsATATT NCBI36
NG_023199.1:g.15643_15647delinsATATT , LRG_314:g.15643_15647delinsATATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.269_273delinsATATT ENSP00000464056.2:p.His90=
ENST00000697677.1:n.1701_1705delinsATATT
ENST00000697678.1:n.522_526delinsATATT
ENST00000697679.1:n.1694_1698delinsATATT
ENST00000697680.1:c.*1484_*1488delinsATATT ENSP00000513392.1:n.*1484_*1488delinsATATT
ENST00000697681.1:c.*1636_*1640delinsATATT ENSP00000513393.1:n.*1636_*1640delinsATATT
ENST00000697683.1:c.*1484_*1488delinsATATT ENSP00000513395.1:n.*1484_*1488delinsATATT
ENST00000697684.1:n.680_684delinsATATT
ENST00000697685.1:c.*1317_*1321delinsATATT ENSP00000513396.1:n.*1317_*1321delinsATATT
ENST00000697686.1:c.269_273delinsATATT ENSP00000513397.1:p.His90=
ENST00000697687.1:n.499_503delinsATATT
ENST00000697688.1:n.666_670delinsATATT
ENST00000697689.1:c.*1156_*1160delinsATATT ENSP00000513398.1:n.*1156_*1160delinsATATT
ENST00000697690.1:c.620_624delinsATATT ENSP00000513399.1:p.His207=
ENST00000697691.1:c.*592_*596delinsATATT ENSP00000513400.1:n.*592_*596delinsATATT
ENST00000697692.1:c.*632_*636delinsATATT ENSP00000513401.1:n.*632_*636delinsATATT
ENST00000697694.1:c.269_273delinsATATT ENSP00000513402.1:p.His90=
ENST00000697695.1:n.1227_1231delinsATATT
ENST00000337432.9:c.620_624delinsATATT MANE Select ENSP00000336701.4:p.His207=
ENST00000337432.8:c.620_624delinsATATT ENSP00000336701.4:p.His207=
ENST00000413590.5:c.258_262delinsATATT
ENST00000425173.5:c.416_420delinsATATT ENSP00000407282.1:p.His139=
ENST00000461271.5:c.269_273delinsATATT ENSP00000464056.1:p.His90=
ENST00000475762.5:c.*1323_*1327delinsATATT ENSP00000432421.1:n.*1323_*1327delinsATATT
ENST00000482007.5:c.*48_*52delinsATATT ENSP00000433332.1:n.*48_*52delinsATATT
ENST00000487525.5:c.*48_*52delinsATATT ENSP00000431637.1:n.*48_*52delinsATATT
ENST00000487921.5:n.532_536delinsATATT
ENST00000583539.5:c.620_624delinsATATT ENSP00000463121.1:p.His207=
ENST00000584617.5:c.342_346delinsATATT
NM_058216.2:c.620_624delinsATATT NP_478123.1:p.His207=
NR_103872.1:n.524_528delinsATATT
XM_006722001.2:c.620_624delinsATATT XP_006722064.1:p.His207=
XM_006722002.2:c.620_624delinsATATT XP_006722065.1:p.His207=
XM_006722004.2:c.269_273delinsATATT XP_006722067.1:p.His90=
XM_006722005.2:c.269_273delinsATATT XP_006722068.1:p.His90=
XM_011525092.1:c.269_273delinsATATT XP_011523394.1:p.His90=
XM_011525093.1:c.269_273delinsATATT XP_011523395.1:p.His90=
XM_011525094.1:c.269_273delinsATATT XP_011523396.1:p.His90=
XR_934513.1:n.693_697delinsATATT
XR_934514.1:n.693_697delinsATATT
XM_006722001.4:c.620_624delinsATATT XP_006722064.1:p.His207=
XM_006722002.4:c.620_624delinsATATT XP_006722065.1:p.His207=
XM_006722004.3:c.269_273delinsATATT XP_006722067.1:p.His90=
XM_006722005.3:c.269_273delinsATATT XP_006722068.1:p.His90=
XM_011525092.2:c.269_273delinsATATT XP_011523394.1:p.His90=
XM_011525093.2:c.269_273delinsATATT XP_011523395.1:p.His90=
XM_011525094.2:c.269_273delinsATATT XP_011523396.1:p.His90=
XM_017024914.1:c.269_273delinsATATT XP_016880403.1:p.His90=
XM_017024915.1:c.269_273delinsATATT XP_016880404.1:p.His90=
XM_017024916.1:c.269_273delinsATATT XP_016880405.1:p.His90=
XM_017024917.1:c.269_273delinsATATT XP_016880406.1:p.His90=
XM_017024918.2:c.269_273delinsATATT XP_016880407.1:p.His90=
XM_017024919.1:c.269_273delinsATATT XP_016880408.1:p.His90=
XR_934513.3:n.1124_1128delinsATATT
XR_934514.3:n.1124_1128delinsATATT
NM_058216.3:c.620_624delinsATATT MANE Select NP_478123.1:p.His207=
NR_103872.2:n.495_499delinsATATT