Canonical Allele Identifier: CA3057242760
Community Standard Title: NM_058216.3(RAD51C):c.669_671delinsGTG (p.Tyr224Cys)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703293_58703295delinsGTG , CM000679.2:g.58703293_58703295delinsGTG GRCh38
NC_000017.10:g.56780654_56780656delinsGTG , CM000679.1:g.56780654_56780656delinsGTG GRCh37
NC_000017.9:g.54135653_54135655delinsGTG NCBI36
NG_023199.1:g.15692_15694delinsGTG , LRG_314:g.15692_15694delinsGTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.669_671delinsGTG MANE Select NP_478123.1:p.Tyr224Cys
ENST00000337432.9:c.669_671delinsGTG MANE Select ENSP00000336701.4:p.Tyr224Cys
NM_058216.2:c.669_671delinsGTG NP_478123.1:p.Tyr224Cys
NR_103872.1:n.573_575delinsGTG
NR_103872.2:n.544_546delinsGTG
ENST00000337432.8:c.669_671delinsGTG ENSP00000336701.4:p.Tyr224Cys
ENST00000413590.5:c.307_309delinsGTG
ENST00000425173.5:c.465_467delinsGTG ENSP00000407282.1:p.Tyr156Cys
ENST00000461271.5:c.318_320delinsGTG ENSP00000464056.1:p.Tyr107Cys
ENST00000461271.6:c.318_320delinsGTG ENSP00000464056.2:p.Tyr107Cys
ENST00000475762.5:c.*1372_*1374delinsGTG ENSP00000432421.1:n.*1372_*1374delinsGTG
ENST00000482007.5:c.*97_*99delinsGTG ENSP00000433332.1:n.*97_*99delinsGTG
ENST00000487525.5:c.*97_*99delinsGTG ENSP00000431637.1:n.*97_*99delinsGTG
ENST00000487921.5:n.581_583delinsGTG
ENST00000583539.5:c.669_671delinsGTG ENSP00000463121.1:p.Tyr224Cys
ENST00000584617.5:c.391_393delinsGTG
ENST00000697677.1:n.1750_1752delinsGTG
ENST00000697678.1:n.571_573delinsGTG
ENST00000697679.1:n.1743_1745delinsGTG
ENST00000697680.1:c.*1533_*1535delinsGTG ENSP00000513392.1:n.*1533_*1535delinsGTG
ENST00000697681.1:c.*1685_*1687delinsGTG ENSP00000513393.1:n.*1685_*1687delinsGTG
ENST00000697683.1:c.*1533_*1535delinsGTG ENSP00000513395.1:n.*1533_*1535delinsGTG
ENST00000697684.1:n.729_731delinsGTG
ENST00000697685.1:c.*1366_*1368delinsGTG ENSP00000513396.1:n.*1366_*1368delinsGTG
ENST00000697686.1:c.318_320delinsGTG ENSP00000513397.1:p.Tyr107Cys
ENST00000697687.1:n.548_550delinsGTG
ENST00000697688.1:n.715_717delinsGTG
ENST00000697689.1:c.*1205_*1207delinsGTG ENSP00000513398.1:n.*1205_*1207delinsGTG
ENST00000697690.1:c.669_671delinsGTG ENSP00000513399.1:p.Tyr224Cys
ENST00000697691.1:c.*641_*643delinsGTG ENSP00000513400.1:n.*641_*643delinsGTG
ENST00000697692.1:c.*681_*683delinsGTG ENSP00000513401.1:n.*681_*683delinsGTG
ENST00000697694.1:c.318_320delinsGTG ENSP00000513402.1:p.Tyr107Cys
ENST00000697695.1:n.1276_1278delinsGTG
XM_006722001.2:c.669_671delinsGTG XP_006722064.1:p.Tyr224Cys
XM_006722001.4:c.669_671delinsGTG XP_006722064.1:p.Tyr224Cys
XM_006722002.2:c.669_671delinsGTG XP_006722065.1:p.Tyr224Cys
XM_006722002.4:c.669_671delinsGTG XP_006722065.1:p.Tyr224Cys
XM_006722004.2:c.318_320delinsGTG XP_006722067.1:p.Tyr107Cys
XM_006722004.3:c.318_320delinsGTG XP_006722067.1:p.Tyr107Cys
XM_006722005.2:c.318_320delinsGTG XP_006722068.1:p.Tyr107Cys
XM_006722005.3:c.318_320delinsGTG XP_006722068.1:p.Tyr107Cys
XM_011525092.1:c.318_320delinsGTG XP_011523394.1:p.Tyr107Cys
XM_011525092.2:c.318_320delinsGTG XP_011523394.1:p.Tyr107Cys
XM_011525093.1:c.318_320delinsGTG XP_011523395.1:p.Tyr107Cys
XM_011525093.2:c.318_320delinsGTG XP_011523395.1:p.Tyr107Cys
XM_011525094.1:c.318_320delinsGTG XP_011523396.1:p.Tyr107Cys
XM_011525094.2:c.318_320delinsGTG XP_011523396.1:p.Tyr107Cys
XM_017024914.1:c.318_320delinsGTG XP_016880403.1:p.Tyr107Cys
XM_017024915.1:c.318_320delinsGTG XP_016880404.1:p.Tyr107Cys
XM_017024916.1:c.318_320delinsGTG XP_016880405.1:p.Tyr107Cys
XM_017024917.1:c.318_320delinsGTG XP_016880406.1:p.Tyr107Cys
XM_017024918.2:c.318_320delinsGTG XP_016880407.1:p.Tyr107Cys
XM_017024919.1:c.318_320delinsGTG XP_016880408.1:p.Tyr107Cys
XR_934513.1:n.742_744delinsGTG
XR_934513.3:n.1173_1175delinsGTG
XR_934514.1:n.742_744delinsGTG
XR_934514.3:n.1173_1175delinsGTG