Canonical Allele Identifier: CA3261180517
Community Standard Title: NM_058216.3(RAD51C):c.1085_1086delinsTT (p.Ser362Phe)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734176_58734177delinsTT , CM000679.2:g.58734176_58734177delinsTT GRCh38
NC_000017.10:g.56811537_56811538delinsTT , CM000679.1:g.56811537_56811538delinsTT GRCh37
NC_000017.9:g.54166536_54166537delinsTT NCBI36
NG_023199.1:g.46575_46576delinsTT , LRG_314:g.46575_46576delinsTT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1085_1086delinsTT MANE Select NP_478123.1:p.Ser362Phe
ENST00000337432.9:c.1085_1086delinsTT MANE Select ENSP00000336701.4:p.Ser362Phe
NM_058216.2:c.1085_1086delinsTT NP_478123.1:p.Ser362Phe
NR_103872.1:n.989_990delinsTT
NR_103872.2:n.960_961delinsTT
ENST00000337432.8:c.1085_1086delinsTT ENSP00000336701.4:p.Ser362Phe
ENST00000413590.5:c.726_727delinsTT
ENST00000461271.6:c.*1617_*1618delinsTT ENSP00000464056.2:n.*1617_*1618delinsTT
ENST00000461706.1:n.272_273delinsTT
ENST00000475762.5:c.*1721_*1722delinsTT ENSP00000432421.1:n.*1721_*1722delinsTT
ENST00000482007.5:c.*513_*514delinsTT ENSP00000433332.1:n.*513_*514delinsTT
ENST00000487525.5:c.*661_*662delinsTT ENSP00000431637.1:n.*661_*662delinsTT
ENST00000578151.1:n.298_299delinsTT
ENST00000581221.5:n.600_601delinsTT
ENST00000584804.1:c.319_320delinsTT ENSP00000463658.1:p.Pro107Phe
ENST00000697680.1:c.*2049_*2050delinsTT ENSP00000513392.1:n.*2049_*2050delinsTT
ENST00000697681.1:c.*2246_*2247delinsTT ENSP00000513393.1:n.*2246_*2247delinsTT
ENST00000697683.1:c.*2021_*2022delinsTT ENSP00000513395.1:n.*2021_*2022delinsTT
ENST00000697685.1:c.*1782_*1783delinsTT ENSP00000513396.1:n.*1782_*1783delinsTT
ENST00000697686.1:c.856_857delinsTT ENSP00000513397.1:p.Pro286Phe
ENST00000697689.1:c.*1499_*1500delinsTT ENSP00000513398.1:n.*1499_*1500delinsTT
ENST00000697690.1:c.*45_*46delinsTT ENSP00000513399.1:n.*45_*46delinsTT
ENST00000697691.1:c.*1057_*1058delinsTT ENSP00000513400.1:n.*1057_*1058delinsTT
ENST00000697692.1:c.*1097_*1098delinsTT ENSP00000513401.1:n.*1097_*1098delinsTT
ENST00000697694.1:c.734_735delinsTT ENSP00000513402.1:p.Ser245Phe
ENST00000697695.1:n.1692_1693delinsTT
XM_006722001.2:c.1088_1089delinsTT XP_006722064.1:p.Ser363Phe
XM_006722001.4:c.1088_1089delinsTT XP_006722064.1:p.Ser363Phe
XM_006722002.2:c.1024_1025delinsTT XP_006722065.1:p.Pro342Phe
XM_006722002.4:c.1024_1025delinsTT XP_006722065.1:p.Pro342Phe
XM_006722004.2:c.737_738delinsTT XP_006722067.1:p.Ser246Phe
XM_006722004.3:c.737_738delinsTT XP_006722067.1:p.Ser246Phe
XM_006722005.2:c.737_738delinsTT XP_006722068.1:p.Ser246Phe
XM_006722005.3:c.737_738delinsTT XP_006722068.1:p.Ser246Phe
XM_011525092.1:c.737_738delinsTT XP_011523394.1:p.Ser246Phe
XM_011525092.2:c.737_738delinsTT XP_011523394.1:p.Ser246Phe
XM_011525093.1:c.737_738delinsTT XP_011523395.1:p.Ser246Phe
XM_011525093.2:c.737_738delinsTT XP_011523395.1:p.Ser246Phe
XM_011525094.1:c.737_738delinsTT XP_011523396.1:p.Ser246Phe
XM_011525094.2:c.737_738delinsTT XP_011523396.1:p.Ser246Phe
XM_017024914.1:c.734_735delinsTT XP_016880403.1:p.Ser245Phe
XM_017024915.1:c.734_735delinsTT XP_016880404.1:p.Ser245Phe
XM_017024916.1:c.734_735delinsTT XP_016880405.1:p.Ser245Phe
XM_017024917.1:c.734_735delinsTT XP_016880406.1:p.Ser245Phe
XM_017024918.2:c.734_735delinsTT XP_016880407.1:p.Ser245Phe
XM_017024919.1:c.673_674delinsTT XP_016880408.1:p.Pro225Phe
XR_934513.1:n.1303_1304delinsTT
XR_934513.3:n.1734_1735delinsTT
XR_934514.1:n.1306_1307delinsTT
XR_934514.3:n.1737_1738delinsTT
XR_934886.1:n.149+3894_149+3895delinsAA
XR_934886.2:n.149+3894_149+3895delinsAA