Canonical Allele Identifier: CA2267829095
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58724065A= , CM000679.2:g.58724065A= GRCh38
NC_000017.10:g.56801426A= , CM000679.1:g.56801426A= GRCh37
NC_000017.9:g.54156425A= NCBI36
NG_023199.1:g.36464A= , LRG_314:g.36464A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.579A= ENSP00000464056.2:p.Thr193=
ENST00000697680.1:c.*1894A= ENSP00000513392.1:n.*1894A=
ENST00000697681.1:c.*2091A= ENSP00000513393.1:n.*2091A=
ENST00000697683.1:c.*1794A= ENSP00000513395.1:n.*1794A=
ENST00000697684.1:n.990A=
ENST00000697685.1:c.*1627A= ENSP00000513396.1:n.*1627A=
ENST00000697686.1:c.579A= ENSP00000513397.1:p.Thr193=
ENST00000697687.1:n.809A=
ENST00000697688.1:n.976A=
ENST00000697689.1:c.*1440+3253A= ENSP00000513398.1:n.*1440+3253A=
ENST00000697690.1:c.904+3253A= ENSP00000513399.1:n.904+3253A=
ENST00000697691.1:c.*902A= ENSP00000513400.1:n.*902A=
ENST00000697692.1:c.*942A= ENSP00000513401.1:n.*942A=
ENST00000697694.1:c.579A= ENSP00000513402.1:p.Thr193=
ENST00000697695.1:n.1537A=
ENST00000337432.9:c.930A= MANE Select ENSP00000336701.4:p.Thr310=
ENST00000337432.8:c.930A= ENSP00000336701.4:p.Thr310=
ENST00000413590.5:c.568A=
ENST00000475762.5:c.*1566A= ENSP00000432421.1:n.*1566A=
ENST00000482007.5:c.*358A= ENSP00000433332.1:n.*358A=
ENST00000487525.5:c.*503A= ENSP00000431637.1:n.*503A=
ENST00000578151.1:n.239+3253A=
ENST00000581221.5:n.445A=
ENST00000583539.5:c.930A= ENSP00000463121.1:p.Thr310=
ENST00000584617.5:c.652A=
ENST00000584804.1:c.199+3253A= ENSP00000463658.1:n.199+3253A=
NM_058216.2:c.930A= NP_478123.1:p.Thr310=
NR_103872.1:n.834A=
XM_006722001.2:c.930A= XP_006722064.1:p.Thr310=
XM_006722002.2:c.904+3253A= XP_006722065.1:n.904+3253A=
XM_006722004.2:c.579A= XP_006722067.1:p.Thr193=
XM_006722005.2:c.579A= XP_006722068.1:p.Thr193=
XM_011525092.1:c.579A= XP_011523394.1:p.Thr193=
XM_011525093.1:c.579A= XP_011523395.1:p.Thr193=
XM_011525094.1:c.579A= XP_011523396.1:p.Thr193=
XR_934513.1:n.1148A=
XR_934514.1:n.1148A=
XM_006722001.4:c.930A= XP_006722064.1:p.Thr310=
XM_006722002.4:c.904+3253A= XP_006722065.1:n.904+3253A=
XM_006722004.3:c.579A= XP_006722067.1:p.Thr193=
XM_006722005.3:c.579A= XP_006722068.1:p.Thr193=
XM_011525092.2:c.579A= XP_011523394.1:p.Thr193=
XM_011525093.2:c.579A= XP_011523395.1:p.Thr193=
XM_011525094.2:c.579A= XP_011523396.1:p.Thr193=
XM_017024914.1:c.579A= XP_016880403.1:p.Thr193=
XM_017024915.1:c.579A= XP_016880404.1:p.Thr193=
XM_017024916.1:c.579A= XP_016880405.1:p.Thr193=
XM_017024917.1:c.579A= XP_016880406.1:p.Thr193=
XM_017024918.2:c.579A= XP_016880407.1:p.Thr193=
XM_017024919.1:c.553+3253A= XP_016880408.1:n.553+3253A=
XR_934513.3:n.1579A=
XR_934514.3:n.1579A=
NM_058216.3:c.930A= MANE Select NP_478123.1:p.Thr310=
NR_103872.2:n.805A=