Canonical Allele Identifier: CA3057242505

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703254_58703256delinsATC , CM000679.2:g.58703254_58703256delinsATC	GRCh38
NC_000017.10:g.56780615_56780617delinsATC , CM000679.1:g.56780615_56780617delinsATC	GRCh37
NC_000017.9:g.54135614_54135616delinsATC	NCBI36
NG_023199.1:g.15653_15655delinsATC , LRG_314:g.15653_15655delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.279_281delinsATC	ENSP00000464056.2:p.Tyr93Ter
ENST00000697677.1:n.1711_1713delinsATC
ENST00000697678.1:n.532_534delinsATC
ENST00000697679.1:n.1704_1706delinsATC
ENST00000697680.1:c.*1494_*1496delinsATC	ENSP00000513392.1:n.*1494_*1496delinsATC
ENST00000697681.1:c.*1646_*1648delinsATC	ENSP00000513393.1:n.*1646_*1648delinsATC
ENST00000697683.1:c.*1494_*1496delinsATC	ENSP00000513395.1:n.*1494_*1496delinsATC
ENST00000697684.1:n.690_692delinsATC
ENST00000697685.1:c.*1327_*1329delinsATC	ENSP00000513396.1:n.*1327_*1329delinsATC
ENST00000697686.1:c.279_281delinsATC	ENSP00000513397.1:p.Tyr93Ter
ENST00000697687.1:n.509_511delinsATC
ENST00000697688.1:n.676_678delinsATC
ENST00000697689.1:c.*1166_*1168delinsATC	ENSP00000513398.1:n.*1166_*1168delinsATC
ENST00000697690.1:c.630_632delinsATC	ENSP00000513399.1:p.Tyr210Ter
ENST00000697691.1:c.*602_*604delinsATC	ENSP00000513400.1:n.*602_*604delinsATC
ENST00000697692.1:c.*642_*644delinsATC	ENSP00000513401.1:n.*642_*644delinsATC
ENST00000697694.1:c.279_281delinsATC	ENSP00000513402.1:p.Tyr93Ter
ENST00000697695.1:n.1237_1239delinsATC
ENST00000337432.9:c.630_632delinsATC MANE Select	ENSP00000336701.4:p.Tyr210Ter
ENST00000337432.8:c.630_632delinsATC	ENSP00000336701.4:p.Tyr210Ter
ENST00000413590.5:c.268_270delinsATC
ENST00000425173.5:c.426_428delinsATC	ENSP00000407282.1:p.Tyr142Ter
ENST00000461271.5:c.279_281delinsATC	ENSP00000464056.1:p.Tyr93Ter
ENST00000475762.5:c.*1333_*1335delinsATC	ENSP00000432421.1:n.*1333_*1335delinsATC
ENST00000482007.5:c.*58_*60delinsATC	ENSP00000433332.1:n.*58_*60delinsATC
ENST00000487525.5:c.*58_*60delinsATC	ENSP00000431637.1:n.*58_*60delinsATC
ENST00000487921.5:n.542_544delinsATC
ENST00000583539.5:c.630_632delinsATC	ENSP00000463121.1:p.Tyr210Ter
ENST00000584617.5:c.352_354delinsATC
NM_058216.2:c.630_632delinsATC	NP_478123.1:p.Tyr210Ter
NR_103872.1:n.534_536delinsATC
XM_006722001.2:c.630_632delinsATC	XP_006722064.1:p.Tyr210Ter
XM_006722002.2:c.630_632delinsATC	XP_006722065.1:p.Tyr210Ter
XM_006722004.2:c.279_281delinsATC	XP_006722067.1:p.Tyr93Ter
XM_006722005.2:c.279_281delinsATC	XP_006722068.1:p.Tyr93Ter
XM_011525092.1:c.279_281delinsATC	XP_011523394.1:p.Tyr93Ter
XM_011525093.1:c.279_281delinsATC	XP_011523395.1:p.Tyr93Ter
XM_011525094.1:c.279_281delinsATC	XP_011523396.1:p.Tyr93Ter
XR_934513.1:n.703_705delinsATC
XR_934514.1:n.703_705delinsATC
XM_006722001.4:c.630_632delinsATC	XP_006722064.1:p.Tyr210Ter
XM_006722002.4:c.630_632delinsATC	XP_006722065.1:p.Tyr210Ter
XM_006722004.3:c.279_281delinsATC	XP_006722067.1:p.Tyr93Ter
XM_006722005.3:c.279_281delinsATC	XP_006722068.1:p.Tyr93Ter
XM_011525092.2:c.279_281delinsATC	XP_011523394.1:p.Tyr93Ter
XM_011525093.2:c.279_281delinsATC	XP_011523395.1:p.Tyr93Ter
XM_011525094.2:c.279_281delinsATC	XP_011523396.1:p.Tyr93Ter
XM_017024914.1:c.279_281delinsATC	XP_016880403.1:p.Tyr93Ter
XM_017024915.1:c.279_281delinsATC	XP_016880404.1:p.Tyr93Ter
XM_017024916.1:c.279_281delinsATC	XP_016880405.1:p.Tyr93Ter
XM_017024917.1:c.279_281delinsATC	XP_016880406.1:p.Tyr93Ter
XM_017024918.2:c.279_281delinsATC	XP_016880407.1:p.Tyr93Ter
XM_017024919.1:c.279_281delinsATC	XP_016880408.1:p.Tyr93Ter
XR_934513.3:n.1134_1136delinsATC
XR_934514.3:n.1134_1136delinsATC
NM_058216.3:c.630_632delinsATC MANE Select	NP_478123.1:p.Tyr210Ter
NR_103872.2:n.505_507delinsATC