Canonical Allele Identifier: CA2267822540
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709964A= , CM000679.2:g.58709964A= GRCh38
NC_000017.10:g.56787325A= , CM000679.1:g.56787325A= GRCh37
NC_000017.9:g.54142324A= NCBI36
NG_023199.1:g.22363A= , LRG_314:g.22363A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.460A= ENSP00000464056.2:p.Ser154=
ENST00000697678.1:n.713A=
ENST00000697679.1:n.1885A=
ENST00000697680.1:c.*1675A= ENSP00000513392.1:n.*1675A=
ENST00000697681.1:c.*1972A= ENSP00000513393.1:n.*1972A=
ENST00000697683.1:c.*1675A= ENSP00000513395.1:n.*1675A=
ENST00000697684.1:n.871A=
ENST00000697685.1:c.*1508A= ENSP00000513396.1:n.*1508A=
ENST00000697686.1:c.460A= ENSP00000513397.1:p.Ser154=
ENST00000697687.1:n.690A=
ENST00000697688.1:n.857A=
ENST00000697689.1:c.*1347A= ENSP00000513398.1:n.*1347A=
ENST00000697690.1:c.811A= ENSP00000513399.1:p.Ser271=
ENST00000697691.1:c.*783A= ENSP00000513400.1:n.*783A=
ENST00000697692.1:c.*823A= ENSP00000513401.1:n.*823A=
ENST00000697694.1:c.460A= ENSP00000513402.1:p.Ser154=
ENST00000697695.1:n.1418A=
ENST00000337432.9:c.811A= MANE Select ENSP00000336701.4:p.Ser271=
ENST00000337432.8:c.811A= ENSP00000336701.4:p.Ser271=
ENST00000413590.5:c.449A=
ENST00000475762.5:c.*1514A= ENSP00000432421.1:n.*1514A=
ENST00000482007.5:c.*239A= ENSP00000433332.1:n.*239A=
ENST00000487525.5:c.*384A= ENSP00000431637.1:n.*384A=
ENST00000578151.1:n.146A=
ENST00000581221.5:n.326A=
ENST00000583539.5:c.811A= ENSP00000463121.1:p.Ser271=
ENST00000584617.5:c.533A=
ENST00000584804.1:c.106A= ENSP00000463658.1:p.Ser36=
NM_058216.2:c.811A= NP_478123.1:p.Ser271=
NR_103872.1:n.715A=
XM_006722001.2:c.811A= XP_006722064.1:p.Ser271=
XM_006722002.2:c.811A= XP_006722065.1:p.Ser271=
XM_006722004.2:c.460A= XP_006722067.1:p.Ser154=
XM_006722005.2:c.460A= XP_006722068.1:p.Ser154=
XM_011525092.1:c.460A= XP_011523394.1:p.Ser154=
XM_011525093.1:c.460A= XP_011523395.1:p.Ser154=
XM_011525094.1:c.460A= XP_011523396.1:p.Ser154=
XR_934513.1:n.1029A=
XR_934514.1:n.1029A=
XM_006722001.4:c.811A= XP_006722064.1:p.Ser271=
XM_006722002.4:c.811A= XP_006722065.1:p.Ser271=
XM_006722004.3:c.460A= XP_006722067.1:p.Ser154=
XM_006722005.3:c.460A= XP_006722068.1:p.Ser154=
XM_011525092.2:c.460A= XP_011523394.1:p.Ser154=
XM_011525093.2:c.460A= XP_011523395.1:p.Ser154=
XM_011525094.2:c.460A= XP_011523396.1:p.Ser154=
XM_017024914.1:c.460A= XP_016880403.1:p.Ser154=
XM_017024915.1:c.460A= XP_016880404.1:p.Ser154=
XM_017024916.1:c.460A= XP_016880405.1:p.Ser154=
XM_017024917.1:c.460A= XP_016880406.1:p.Ser154=
XM_017024918.2:c.460A= XP_016880407.1:p.Ser154=
XM_017024919.1:c.460A= XP_016880408.1:p.Ser154=
XR_934513.3:n.1460A=
XR_934514.3:n.1460A=
NM_058216.3:c.811A= MANE Select NP_478123.1:p.Ser271=
NR_103872.2:n.686A=