Canonical Allele Identifier: CA3057243539
Community Standard Title: NM_058216.3(RAD51C):c.1083_1085delinsCTT (p.Ser362Phe)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734174_58734176delinsCTT , CM000679.2:g.58734174_58734176delinsCTT GRCh38
NC_000017.10:g.56811535_56811537delinsCTT , CM000679.1:g.56811535_56811537delinsCTT GRCh37
NC_000017.9:g.54166534_54166536delinsCTT NCBI36
NG_023199.1:g.46573_46575delinsCTT , LRG_314:g.46573_46575delinsCTT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1083_1085delinsCTT MANE Select NP_478123.1:p.Ser362Phe
ENST00000337432.9:c.1083_1085delinsCTT MANE Select ENSP00000336701.4:p.Ser362Phe
NM_058216.2:c.1083_1085delinsCTT NP_478123.1:p.Ser362Phe
NR_103872.1:n.987_989delinsCTT
NR_103872.2:n.958_960delinsCTT
ENST00000337432.8:c.1083_1085delinsCTT ENSP00000336701.4:p.Ser362Phe
ENST00000413590.5:c.724_726delinsCTT
ENST00000461271.6:c.*1615_*1617delinsCTT ENSP00000464056.2:n.*1615_*1617delinsCTT
ENST00000461706.1:n.270_272delinsCTT
ENST00000475762.5:c.*1719_*1721delinsCTT ENSP00000432421.1:n.*1719_*1721delinsCTT
ENST00000482007.5:c.*511_*513delinsCTT ENSP00000433332.1:n.*511_*513delinsCTT
ENST00000487525.5:c.*659_*661delinsCTT ENSP00000431637.1:n.*659_*661delinsCTT
ENST00000578151.1:n.296_298delinsCTT
ENST00000581221.5:n.598_600delinsCTT
ENST00000584804.1:c.317_319delinsCTT ENSP00000463658.1:p.Val106_Pro107delinsAlaSer
ENST00000697680.1:c.*2047_*2049delinsCTT ENSP00000513392.1:n.*2047_*2049delinsCTT
ENST00000697681.1:c.*2244_*2246delinsCTT ENSP00000513393.1:n.*2244_*2246delinsCTT
ENST00000697683.1:c.*2019_*2021delinsCTT ENSP00000513395.1:n.*2019_*2021delinsCTT
ENST00000697685.1:c.*1780_*1782delinsCTT ENSP00000513396.1:n.*1780_*1782delinsCTT
ENST00000697686.1:c.854_856delinsCTT ENSP00000513397.1:p.Val285_Pro286delinsAlaSer
ENST00000697689.1:c.*1497_*1499delinsCTT ENSP00000513398.1:n.*1497_*1499delinsCTT
ENST00000697690.1:c.*43_*45delinsCTT ENSP00000513399.1:n.*43_*45delinsCTT
ENST00000697691.1:c.*1055_*1057delinsCTT ENSP00000513400.1:n.*1055_*1057delinsCTT
ENST00000697692.1:c.*1095_*1097delinsCTT ENSP00000513401.1:n.*1095_*1097delinsCTT
ENST00000697694.1:c.732_734delinsCTT ENSP00000513402.1:p.Ser245Phe
ENST00000697695.1:n.1690_1692delinsCTT
XM_006722001.2:c.1086_1088delinsCTT XP_006722064.1:p.Ser363Phe
XM_006722001.4:c.1086_1088delinsCTT XP_006722064.1:p.Ser363Phe
XM_006722002.2:c.1022_1024delinsCTT XP_006722065.1:p.Val341_Pro342delinsAlaSer
XM_006722002.4:c.1022_1024delinsCTT XP_006722065.1:p.Val341_Pro342delinsAlaSer
XM_006722004.2:c.735_737delinsCTT XP_006722067.1:p.Ser246Phe
XM_006722004.3:c.735_737delinsCTT XP_006722067.1:p.Ser246Phe
XM_006722005.2:c.735_737delinsCTT XP_006722068.1:p.Ser246Phe
XM_006722005.3:c.735_737delinsCTT XP_006722068.1:p.Ser246Phe
XM_011525092.1:c.735_737delinsCTT XP_011523394.1:p.Ser246Phe
XM_011525092.2:c.735_737delinsCTT XP_011523394.1:p.Ser246Phe
XM_011525093.1:c.735_737delinsCTT XP_011523395.1:p.Ser246Phe
XM_011525093.2:c.735_737delinsCTT XP_011523395.1:p.Ser246Phe
XM_011525094.1:c.735_737delinsCTT XP_011523396.1:p.Ser246Phe
XM_011525094.2:c.735_737delinsCTT XP_011523396.1:p.Ser246Phe
XM_017024914.1:c.732_734delinsCTT XP_016880403.1:p.Ser245Phe
XM_017024915.1:c.732_734delinsCTT XP_016880404.1:p.Ser245Phe
XM_017024916.1:c.732_734delinsCTT XP_016880405.1:p.Ser245Phe
XM_017024917.1:c.732_734delinsCTT XP_016880406.1:p.Ser245Phe
XM_017024918.2:c.732_734delinsCTT XP_016880407.1:p.Ser245Phe
XM_017024919.1:c.671_673delinsCTT XP_016880408.1:p.Val224_Pro225delinsAlaSer
XR_934513.1:n.1301_1303delinsCTT
XR_934513.3:n.1732_1734delinsCTT
XR_934514.1:n.1304_1306delinsCTT
XR_934514.3:n.1735_1737delinsCTT
XR_934886.1:n.149+3895_149+3897delinsAAG
XR_934886.2:n.149+3895_149+3897delinsAAG