Canonical Allele Identifier: CA2267822481
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709874G= , CM000679.2:g.58709874G= GRCh38
NC_000017.10:g.56787235G= , CM000679.1:g.56787235G= GRCh37
NC_000017.9:g.54142234G= NCBI36
NG_023199.1:g.22273G= , LRG_314:g.22273G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.370G= ENSP00000464056.2:p.Val124=
ENST00000697678.1:n.623G=
ENST00000697679.1:n.1795G=
ENST00000697680.1:c.*1585G= ENSP00000513392.1:n.*1585G=
ENST00000697681.1:c.*1882G= ENSP00000513393.1:n.*1882G=
ENST00000697683.1:c.*1585G= ENSP00000513395.1:n.*1585G=
ENST00000697684.1:n.781G=
ENST00000697685.1:c.*1418G= ENSP00000513396.1:n.*1418G=
ENST00000697686.1:c.370G= ENSP00000513397.1:p.Val124=
ENST00000697687.1:n.600G=
ENST00000697688.1:n.767G=
ENST00000697689.1:c.*1257G= ENSP00000513398.1:n.*1257G=
ENST00000697690.1:c.721G= ENSP00000513399.1:p.Val241=
ENST00000697691.1:c.*693G= ENSP00000513400.1:n.*693G=
ENST00000697692.1:c.*733G= ENSP00000513401.1:n.*733G=
ENST00000697694.1:c.370G= ENSP00000513402.1:p.Val124=
ENST00000697695.1:n.1328G=
ENST00000337432.9:c.721G= MANE Select ENSP00000336701.4:p.Val241=
ENST00000337432.8:c.721G= ENSP00000336701.4:p.Val241=
ENST00000413590.5:c.359G=
ENST00000425173.5:c.637G= ENSP00000407282.1:p.Val213=
ENST00000461271.5:c.370G= ENSP00000464056.1:p.Val124=
ENST00000475762.5:c.*1424G= ENSP00000432421.1:n.*1424G=
ENST00000482007.5:c.*149G= ENSP00000433332.1:n.*149G=
ENST00000487525.5:c.*294G= ENSP00000431637.1:n.*294G=
ENST00000578151.1:n.56G=
ENST00000581221.5:n.236G=
ENST00000583539.5:c.721G= ENSP00000463121.1:p.Val241=
ENST00000584617.5:c.443G=
ENST00000584804.1:c.16G= ENSP00000463658.1:p.Val6=
NM_058216.2:c.721G= NP_478123.1:p.Val241=
NR_103872.1:n.625G=
XM_006722001.2:c.721G= XP_006722064.1:p.Val241=
XM_006722002.2:c.721G= XP_006722065.1:p.Val241=
XM_006722004.2:c.370G= XP_006722067.1:p.Val124=
XM_006722005.2:c.370G= XP_006722068.1:p.Val124=
XM_011525092.1:c.370G= XP_011523394.1:p.Val124=
XM_011525093.1:c.370G= XP_011523395.1:p.Val124=
XM_011525094.1:c.370G= XP_011523396.1:p.Val124=
XR_934513.1:n.939G=
XR_934514.1:n.939G=
XM_006722001.4:c.721G= XP_006722064.1:p.Val241=
XM_006722002.4:c.721G= XP_006722065.1:p.Val241=
XM_006722004.3:c.370G= XP_006722067.1:p.Val124=
XM_006722005.3:c.370G= XP_006722068.1:p.Val124=
XM_011525092.2:c.370G= XP_011523394.1:p.Val124=
XM_011525093.2:c.370G= XP_011523395.1:p.Val124=
XM_011525094.2:c.370G= XP_011523396.1:p.Val124=
XM_017024914.1:c.370G= XP_016880403.1:p.Val124=
XM_017024915.1:c.370G= XP_016880404.1:p.Val124=
XM_017024916.1:c.370G= XP_016880405.1:p.Val124=
XM_017024917.1:c.370G= XP_016880406.1:p.Val124=
XM_017024918.2:c.370G= XP_016880407.1:p.Val124=
XM_017024919.1:c.370G= XP_016880408.1:p.Val124=
XR_934513.3:n.1370G=
XR_934514.3:n.1370G=
NM_058216.3:c.721G= MANE Select NP_478123.1:p.Val241=
NR_103872.2:n.596G=