Canonical Allele Identifier: CA3261179926
Community Standard Title: NM_058216.3(RAD51C):c.1048_1050delinsTTC (p.Val350Phe)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734139_58734141delinsTTC , CM000679.2:g.58734139_58734141delinsTTC GRCh38
NC_000017.10:g.56811500_56811502delinsTTC , CM000679.1:g.56811500_56811502delinsTTC GRCh37
NC_000017.9:g.54166499_54166501delinsTTC NCBI36
NG_023199.1:g.46538_46540delinsTTC , LRG_314:g.46538_46540delinsTTC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1048_1050delinsTTC MANE Select NP_478123.1:p.Val350Phe
ENST00000337432.9:c.1048_1050delinsTTC MANE Select ENSP00000336701.4:p.Val350Phe
NM_058216.2:c.1048_1050delinsTTC NP_478123.1:p.Val350Phe
NR_103872.1:n.952_954delinsTTC
NR_103872.2:n.923_925delinsTTC
ENST00000337432.8:c.1048_1050delinsTTC ENSP00000336701.4:p.Val350Phe
ENST00000413590.5:c.689_691delinsTTC
ENST00000461271.6:c.*1580_*1582delinsTTC ENSP00000464056.2:n.*1580_*1582delinsTTC
ENST00000461706.1:n.235_237delinsTTC
ENST00000475762.5:c.*1684_*1686delinsTTC ENSP00000432421.1:n.*1684_*1686delinsTTC
ENST00000482007.5:c.*476_*478delinsTTC ENSP00000433332.1:n.*476_*478delinsTTC
ENST00000487525.5:c.*624_*626delinsTTC ENSP00000431637.1:n.*624_*626delinsTTC
ENST00000578151.1:n.261_263delinsTTC
ENST00000581221.5:n.563_565delinsTTC
ENST00000584804.1:c.282_284delinsTTC ENSP00000463658.1:p.Leu95Ser
ENST00000697680.1:c.*2012_*2014delinsTTC ENSP00000513392.1:n.*2012_*2014delinsTTC
ENST00000697681.1:c.*2209_*2211delinsTTC ENSP00000513393.1:n.*2209_*2211delinsTTC
ENST00000697683.1:c.*1984_*1986delinsTTC ENSP00000513395.1:n.*1984_*1986delinsTTC
ENST00000697685.1:c.*1745_*1747delinsTTC ENSP00000513396.1:n.*1745_*1747delinsTTC
ENST00000697686.1:c.819_821delinsTTC ENSP00000513397.1:p.Leu274Ser
ENST00000697689.1:c.*1462_*1464delinsTTC ENSP00000513398.1:n.*1462_*1464delinsTTC
ENST00000697690.1:c.*8_*10delinsTTC ENSP00000513399.1:n.*8_*10delinsTTC
ENST00000697691.1:c.*1020_*1022delinsTTC ENSP00000513400.1:n.*1020_*1022delinsTTC
ENST00000697692.1:c.*1060_*1062delinsTTC ENSP00000513401.1:n.*1060_*1062delinsTTC
ENST00000697694.1:c.697_699delinsTTC ENSP00000513402.1:p.Val233Phe
ENST00000697695.1:n.1655_1657delinsTTC
XM_006722001.2:c.1051_1053delinsTTC XP_006722064.1:p.Val351Phe
XM_006722001.4:c.1051_1053delinsTTC XP_006722064.1:p.Val351Phe
XM_006722002.2:c.987_989delinsTTC XP_006722065.1:p.Leu330Ser
XM_006722002.4:c.987_989delinsTTC XP_006722065.1:p.Leu330Ser
XM_006722004.2:c.700_702delinsTTC XP_006722067.1:p.Val234Phe
XM_006722004.3:c.700_702delinsTTC XP_006722067.1:p.Val234Phe
XM_006722005.2:c.700_702delinsTTC XP_006722068.1:p.Val234Phe
XM_006722005.3:c.700_702delinsTTC XP_006722068.1:p.Val234Phe
XM_011525092.1:c.700_702delinsTTC XP_011523394.1:p.Val234Phe
XM_011525092.2:c.700_702delinsTTC XP_011523394.1:p.Val234Phe
XM_011525093.1:c.700_702delinsTTC XP_011523395.1:p.Val234Phe
XM_011525093.2:c.700_702delinsTTC XP_011523395.1:p.Val234Phe
XM_011525094.1:c.700_702delinsTTC XP_011523396.1:p.Val234Phe
XM_011525094.2:c.700_702delinsTTC XP_011523396.1:p.Val234Phe
XM_017024914.1:c.697_699delinsTTC XP_016880403.1:p.Val233Phe
XM_017024915.1:c.697_699delinsTTC XP_016880404.1:p.Val233Phe
XM_017024916.1:c.697_699delinsTTC XP_016880405.1:p.Val233Phe
XM_017024917.1:c.697_699delinsTTC XP_016880406.1:p.Val233Phe
XM_017024918.2:c.697_699delinsTTC XP_016880407.1:p.Val233Phe
XM_017024919.1:c.636_638delinsTTC XP_016880408.1:p.Leu213Ser
XR_934513.1:n.1266_1268delinsTTC
XR_934513.3:n.1697_1699delinsTTC
XR_934514.1:n.1269_1271delinsTTC
XR_934514.3:n.1700_1702delinsTTC
XR_934886.1:n.149+3930_149+3932delinsGAA
XR_934886.2:n.149+3930_149+3932delinsGAA