Canonical Allele Identifier: CA2267819492
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703282C= , CM000679.2:g.58703282C= GRCh38
NC_000017.10:g.56780643C= , CM000679.1:g.56780643C= GRCh37
NC_000017.9:g.54135642C= NCBI36
NG_023199.1:g.15681C= , LRG_314:g.15681C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.307C= ENSP00000464056.2:p.Leu103=
ENST00000697677.1:n.1739C=
ENST00000697678.1:n.560C=
ENST00000697679.1:n.1732C=
ENST00000697680.1:c.*1522C= ENSP00000513392.1:n.*1522C=
ENST00000697681.1:c.*1674C= ENSP00000513393.1:n.*1674C=
ENST00000697683.1:c.*1522C= ENSP00000513395.1:n.*1522C=
ENST00000697684.1:n.718C=
ENST00000697685.1:c.*1355C= ENSP00000513396.1:n.*1355C=
ENST00000697686.1:c.307C= ENSP00000513397.1:p.Leu103=
ENST00000697687.1:n.537C=
ENST00000697688.1:n.704C=
ENST00000697689.1:c.*1194C= ENSP00000513398.1:n.*1194C=
ENST00000697690.1:c.658C= ENSP00000513399.1:p.Leu220=
ENST00000697691.1:c.*630C= ENSP00000513400.1:n.*630C=
ENST00000697692.1:c.*670C= ENSP00000513401.1:n.*670C=
ENST00000697694.1:c.307C= ENSP00000513402.1:p.Leu103=
ENST00000697695.1:n.1265C=
ENST00000337432.9:c.658C= MANE Select ENSP00000336701.4:p.Leu220=
ENST00000337432.8:c.658C= ENSP00000336701.4:p.Leu220=
ENST00000413590.5:c.296C=
ENST00000425173.5:c.454C= ENSP00000407282.1:p.Leu152=
ENST00000461271.5:c.307C= ENSP00000464056.1:p.Leu103=
ENST00000475762.5:c.*1361C= ENSP00000432421.1:n.*1361C=
ENST00000482007.5:c.*86C= ENSP00000433332.1:n.*86C=
ENST00000487525.5:c.*86C= ENSP00000431637.1:n.*86C=
ENST00000487921.5:n.570C=
ENST00000583539.5:c.658C= ENSP00000463121.1:p.Leu220=
ENST00000584617.5:c.380C=
NM_058216.2:c.658C= NP_478123.1:p.Leu220=
NR_103872.1:n.562C=
XM_006722001.2:c.658C= XP_006722064.1:p.Leu220=
XM_006722002.2:c.658C= XP_006722065.1:p.Leu220=
XM_006722004.2:c.307C= XP_006722067.1:p.Leu103=
XM_006722005.2:c.307C= XP_006722068.1:p.Leu103=
XM_011525092.1:c.307C= XP_011523394.1:p.Leu103=
XM_011525093.1:c.307C= XP_011523395.1:p.Leu103=
XM_011525094.1:c.307C= XP_011523396.1:p.Leu103=
XR_934513.1:n.731C=
XR_934514.1:n.731C=
XM_006722001.4:c.658C= XP_006722064.1:p.Leu220=
XM_006722002.4:c.658C= XP_006722065.1:p.Leu220=
XM_006722004.3:c.307C= XP_006722067.1:p.Leu103=
XM_006722005.3:c.307C= XP_006722068.1:p.Leu103=
XM_011525092.2:c.307C= XP_011523394.1:p.Leu103=
XM_011525093.2:c.307C= XP_011523395.1:p.Leu103=
XM_011525094.2:c.307C= XP_011523396.1:p.Leu103=
XM_017024914.1:c.307C= XP_016880403.1:p.Leu103=
XM_017024915.1:c.307C= XP_016880404.1:p.Leu103=
XM_017024916.1:c.307C= XP_016880405.1:p.Leu103=
XM_017024917.1:c.307C= XP_016880406.1:p.Leu103=
XM_017024918.2:c.307C= XP_016880407.1:p.Leu103=
XM_017024919.1:c.307C= XP_016880408.1:p.Leu103=
XR_934513.3:n.1162C=
XR_934514.3:n.1162C=
NM_058216.3:c.658C= MANE Select NP_478123.1:p.Leu220=
NR_103872.2:n.533C=