Canonical Allele Identifier: CA3261180739
Community Standard Title: NM_058216.3(RAD51C):c.1109_1110delinsAG (p.Arg370Gln)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734200_58734201delinsAG , CM000679.2:g.58734200_58734201delinsAG GRCh38
NC_000017.10:g.56811561_56811562delinsAG , CM000679.1:g.56811561_56811562delinsAG GRCh37
NC_000017.9:g.54166560_54166561delinsAG NCBI36
NG_023199.1:g.46599_46600delinsAG , LRG_314:g.46599_46600delinsAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1109_1110delinsAG MANE Select NP_478123.1:p.Arg370Gln
ENST00000337432.9:c.1109_1110delinsAG MANE Select ENSP00000336701.4:p.Arg370Gln
NM_058216.2:c.1109_1110delinsAG NP_478123.1:p.Arg370Gln
NR_103872.1:n.1013_1014delinsAG
NR_103872.2:n.984_985delinsAG
ENST00000337432.8:c.1109_1110delinsAG ENSP00000336701.4:p.Arg370Gln
ENST00000413590.5:c.750_751delinsAG
ENST00000461271.6:c.*1641_*1642delinsAG ENSP00000464056.2:n.*1641_*1642delinsAG
ENST00000461706.1:n.296_297delinsAG
ENST00000475762.5:c.*1745_*1746delinsAG ENSP00000432421.1:n.*1745_*1746delinsAG
ENST00000482007.5:c.*537_*538delinsAG ENSP00000433332.1:n.*537_*538delinsAG
ENST00000487525.5:c.*685_*686delinsAG ENSP00000431637.1:n.*685_*686delinsAG
ENST00000578151.1:n.322_323delinsAG
ENST00000581221.5:n.624_625delinsAG
ENST00000584804.1:c.343_344delinsAG ENSP00000463658.1:n.343_344delinsAG
ENST00000697680.1:c.*2073_*2074delinsAG ENSP00000513392.1:n.*2073_*2074delinsAG
ENST00000697681.1:c.*2270_*2271delinsAG ENSP00000513393.1:n.*2270_*2271delinsAG
ENST00000697683.1:c.*2045_*2046delinsAG ENSP00000513395.1:n.*2045_*2046delinsAG
ENST00000697685.1:c.*1806_*1807delinsAG ENSP00000513396.1:n.*1806_*1807delinsAG
ENST00000697686.1:c.*19_*20delinsAG ENSP00000513397.1:n.*19_*20delinsAG
ENST00000697689.1:c.*1523_*1524delinsAG ENSP00000513398.1:n.*1523_*1524delinsAG
ENST00000697690.1:c.*69_*70delinsAG ENSP00000513399.1:n.*69_*70delinsAG
ENST00000697691.1:c.*1081_*1082delinsAG ENSP00000513400.1:n.*1081_*1082delinsAG
ENST00000697692.1:c.*1121_*1122delinsAG ENSP00000513401.1:n.*1121_*1122delinsAG
ENST00000697694.1:c.758_759delinsAG ENSP00000513402.1:p.Arg253Gln
ENST00000697695.1:n.1716_1717delinsAG
XM_006722001.2:c.1112_1113delinsAG XP_006722064.1:p.Arg371Gln
XM_006722001.4:c.1112_1113delinsAG XP_006722064.1:p.Arg371Gln
XM_006722002.2:c.*19_*20delinsAG XP_006722065.1:n.*19_*20delinsAG
XM_006722002.4:c.*19_*20delinsAG XP_006722065.1:n.*19_*20delinsAG
XM_006722004.2:c.761_762delinsAG XP_006722067.1:p.Arg254Gln
XM_006722004.3:c.761_762delinsAG XP_006722067.1:p.Arg254Gln
XM_006722005.2:c.761_762delinsAG XP_006722068.1:p.Arg254Gln
XM_006722005.3:c.761_762delinsAG XP_006722068.1:p.Arg254Gln
XM_011525092.1:c.761_762delinsAG XP_011523394.1:p.Arg254Gln
XM_011525092.2:c.761_762delinsAG XP_011523394.1:p.Arg254Gln
XM_011525093.1:c.761_762delinsAG XP_011523395.1:p.Arg254Gln
XM_011525093.2:c.761_762delinsAG XP_011523395.1:p.Arg254Gln
XM_011525094.1:c.761_762delinsAG XP_011523396.1:p.Arg254Gln
XM_011525094.2:c.761_762delinsAG XP_011523396.1:p.Arg254Gln
XM_017024914.1:c.758_759delinsAG XP_016880403.1:p.Arg253Gln
XM_017024915.1:c.758_759delinsAG XP_016880404.1:p.Arg253Gln
XM_017024916.1:c.758_759delinsAG XP_016880405.1:p.Arg253Gln
XM_017024917.1:c.758_759delinsAG XP_016880406.1:p.Arg253Gln
XM_017024918.2:c.758_759delinsAG XP_016880407.1:p.Arg253Gln
XM_017024919.1:c.*19_*20delinsAG XP_016880408.1:n.*19_*20delinsAG
XR_934513.1:n.1327_1328delinsAG
XR_934513.3:n.1758_1759delinsAG
XR_934886.1:n.149+3870_149+3871delinsCT
XR_934886.2:n.149+3870_149+3871delinsCT