Canonical Allele Identifier: CA3060598043
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58724057_58724059delinsAGC , CM000679.2:g.58724057_58724059delinsAGC GRCh38
NC_000017.10:g.56801418_56801420delinsAGC , CM000679.1:g.56801418_56801420delinsAGC GRCh37
NC_000017.9:g.54156417_54156419delinsAGC NCBI36
NG_023199.1:g.36456_36458delinsAGC , LRG_314:g.36456_36458delinsAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.571_573delinsAGC ENSP00000464056.2:p.Ala191Ser
ENST00000697680.1:c.*1886_*1888delinsAGC ENSP00000513392.1:n.*1886_*1888delinsAGC
ENST00000697681.1:c.*2083_*2085delinsAGC ENSP00000513393.1:n.*2083_*2085delinsAGC
ENST00000697683.1:c.*1786_*1788delinsAGC ENSP00000513395.1:n.*1786_*1788delinsAGC
ENST00000697684.1:n.982_984delinsAGC
ENST00000697685.1:c.*1619_*1621delinsAGC ENSP00000513396.1:n.*1619_*1621delinsAGC
ENST00000697686.1:c.571_573delinsAGC ENSP00000513397.1:p.Ala191Ser
ENST00000697687.1:n.801_803delinsAGC
ENST00000697688.1:n.968_970delinsAGC
ENST00000697689.1:c.*1440+3245_*1440+3247delinsAGC ENSP00000513398.1:n.*1440+3245_*1440+3247delinsAGC
ENST00000697690.1:c.904+3245_904+3247delinsAGC ENSP00000513399.1:n.904+3245_904+3247delinsAGC
ENST00000697691.1:c.*894_*896delinsAGC ENSP00000513400.1:n.*894_*896delinsAGC
ENST00000697692.1:c.*934_*936delinsAGC ENSP00000513401.1:n.*934_*936delinsAGC
ENST00000697694.1:c.571_573delinsAGC ENSP00000513402.1:p.Ala191Ser
ENST00000697695.1:n.1529_1531delinsAGC
ENST00000337432.9:c.922_924delinsAGC MANE Select ENSP00000336701.4:p.Ala308Ser
ENST00000337432.8:c.922_924delinsAGC ENSP00000336701.4:p.Ala308Ser
ENST00000413590.5:c.560_562delinsAGC
ENST00000475762.5:c.*1558_*1560delinsAGC ENSP00000432421.1:n.*1558_*1560delinsAGC
ENST00000482007.5:c.*350_*352delinsAGC ENSP00000433332.1:n.*350_*352delinsAGC
ENST00000487525.5:c.*495_*497delinsAGC ENSP00000431637.1:n.*495_*497delinsAGC
ENST00000578151.1:n.239+3245_239+3247delinsAGC
ENST00000581221.5:n.437_439delinsAGC
ENST00000583539.5:c.922_924delinsAGC ENSP00000463121.1:p.Ala308Ser
ENST00000584617.5:c.644_646delinsAGC
ENST00000584804.1:c.199+3245_199+3247delinsAGC ENSP00000463658.1:n.199+3245_199+3247delinsAGC
NM_058216.2:c.922_924delinsAGC NP_478123.1:p.Ala308Ser
NR_103872.1:n.826_828delinsAGC
XM_006722001.2:c.922_924delinsAGC XP_006722064.1:p.Ala308Ser
XM_006722002.2:c.904+3245_904+3247delinsAGC XP_006722065.1:n.904+3245_904+3247delinsAGC
XM_006722004.2:c.571_573delinsAGC XP_006722067.1:p.Ala191Ser
XM_006722005.2:c.571_573delinsAGC XP_006722068.1:p.Ala191Ser
XM_011525092.1:c.571_573delinsAGC XP_011523394.1:p.Ala191Ser
XM_011525093.1:c.571_573delinsAGC XP_011523395.1:p.Ala191Ser
XM_011525094.1:c.571_573delinsAGC XP_011523396.1:p.Ala191Ser
XR_934513.1:n.1140_1142delinsAGC
XR_934514.1:n.1140_1142delinsAGC
XM_006722001.4:c.922_924delinsAGC XP_006722064.1:p.Ala308Ser
XM_006722002.4:c.904+3245_904+3247delinsAGC XP_006722065.1:n.904+3245_904+3247delinsAGC
XM_006722004.3:c.571_573delinsAGC XP_006722067.1:p.Ala191Ser
XM_006722005.3:c.571_573delinsAGC XP_006722068.1:p.Ala191Ser
XM_011525092.2:c.571_573delinsAGC XP_011523394.1:p.Ala191Ser
XM_011525093.2:c.571_573delinsAGC XP_011523395.1:p.Ala191Ser
XM_011525094.2:c.571_573delinsAGC XP_011523396.1:p.Ala191Ser
XM_017024914.1:c.571_573delinsAGC XP_016880403.1:p.Ala191Ser
XM_017024915.1:c.571_573delinsAGC XP_016880404.1:p.Ala191Ser
XM_017024916.1:c.571_573delinsAGC XP_016880405.1:p.Ala191Ser
XM_017024917.1:c.571_573delinsAGC XP_016880406.1:p.Ala191Ser
XM_017024918.2:c.571_573delinsAGC XP_016880407.1:p.Ala191Ser
XM_017024919.1:c.553+3245_553+3247delinsAGC XP_016880408.1:n.553+3245_553+3247delinsAGC
XR_934513.3:n.1571_1573delinsAGC
XR_934514.3:n.1571_1573delinsAGC
NM_058216.3:c.922_924delinsAGC MANE Select NP_478123.1:p.Ala308Ser
NR_103872.2:n.797_799delinsAGC