Canonical Allele Identifier: CA2267822475
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709867A= , CM000679.2:g.58709867A= GRCh38
NC_000017.10:g.56787228A= , CM000679.1:g.56787228A= GRCh37
NC_000017.9:g.54142227A= NCBI36
NG_023199.1:g.22266A= , LRG_314:g.22266A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.363A= ENSP00000464056.2:p.Leu121=
ENST00000697678.1:n.616A=
ENST00000697679.1:n.1788A=
ENST00000697680.1:c.*1578A= ENSP00000513392.1:n.*1578A=
ENST00000697681.1:c.*1875A= ENSP00000513393.1:n.*1875A=
ENST00000697683.1:c.*1578A= ENSP00000513395.1:n.*1578A=
ENST00000697684.1:n.774A=
ENST00000697685.1:c.*1411A= ENSP00000513396.1:n.*1411A=
ENST00000697686.1:c.363A= ENSP00000513397.1:p.Leu121=
ENST00000697687.1:n.593A=
ENST00000697688.1:n.760A=
ENST00000697689.1:c.*1250A= ENSP00000513398.1:n.*1250A=
ENST00000697690.1:c.714A= ENSP00000513399.1:p.Leu238=
ENST00000697691.1:c.*686A= ENSP00000513400.1:n.*686A=
ENST00000697692.1:c.*726A= ENSP00000513401.1:n.*726A=
ENST00000697694.1:c.363A= ENSP00000513402.1:p.Leu121=
ENST00000697695.1:n.1321A=
ENST00000337432.9:c.714A= MANE Select ENSP00000336701.4:p.Leu238=
ENST00000337432.8:c.714A= ENSP00000336701.4:p.Leu238=
ENST00000413590.5:c.352A=
ENST00000425173.5:c.630A= ENSP00000407282.1:p.Leu210=
ENST00000461271.5:c.363A= ENSP00000464056.1:p.Leu121=
ENST00000475762.5:c.*1417A= ENSP00000432421.1:n.*1417A=
ENST00000482007.5:c.*142A= ENSP00000433332.1:n.*142A=
ENST00000487525.5:c.*287A= ENSP00000431637.1:n.*287A=
ENST00000578151.1:n.49A=
ENST00000581221.5:n.229A=
ENST00000583539.5:c.714A= ENSP00000463121.1:p.Leu238=
ENST00000584617.5:c.436A=
ENST00000584804.1:c.9A= ENSP00000463658.1:p.Leu3=
NM_058216.2:c.714A= NP_478123.1:p.Leu238=
NR_103872.1:n.618A=
XM_006722001.2:c.714A= XP_006722064.1:p.Leu238=
XM_006722002.2:c.714A= XP_006722065.1:p.Leu238=
XM_006722004.2:c.363A= XP_006722067.1:p.Leu121=
XM_006722005.2:c.363A= XP_006722068.1:p.Leu121=
XM_011525092.1:c.363A= XP_011523394.1:p.Leu121=
XM_011525093.1:c.363A= XP_011523395.1:p.Leu121=
XM_011525094.1:c.363A= XP_011523396.1:p.Leu121=
XR_934513.1:n.932A=
XR_934514.1:n.932A=
XM_006722001.4:c.714A= XP_006722064.1:p.Leu238=
XM_006722002.4:c.714A= XP_006722065.1:p.Leu238=
XM_006722004.3:c.363A= XP_006722067.1:p.Leu121=
XM_006722005.3:c.363A= XP_006722068.1:p.Leu121=
XM_011525092.2:c.363A= XP_011523394.1:p.Leu121=
XM_011525093.2:c.363A= XP_011523395.1:p.Leu121=
XM_011525094.2:c.363A= XP_011523396.1:p.Leu121=
XM_017024914.1:c.363A= XP_016880403.1:p.Leu121=
XM_017024915.1:c.363A= XP_016880404.1:p.Leu121=
XM_017024916.1:c.363A= XP_016880405.1:p.Leu121=
XM_017024917.1:c.363A= XP_016880406.1:p.Leu121=
XM_017024918.2:c.363A= XP_016880407.1:p.Leu121=
XM_017024919.1:c.363A= XP_016880408.1:p.Leu121=
XR_934513.3:n.1363A=
XR_934514.3:n.1363A=
NM_058216.3:c.714A= MANE Select NP_478123.1:p.Leu238=
NR_103872.2:n.589A=