Canonical Allele Identifier: CA2267814301

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58693123_58693125delinsCTT , CM000679.2:g.58693123_58693125delinsCTT	GRCh38
NC_000017.10:g.56770484_56770486delinsCTT , CM000679.1:g.56770484_56770486delinsCTT	GRCh37
NC_000017.9:g.54125483_54125485delinsCTT	NCBI36
NG_023199.1:g.5522_5524delinsCTT , LRG_314:g.5522_5524delinsCTT
NG_047169.1:g.3955_3957delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+438_-207+440delinsCTT	ENSP00000464056.2:n.-207+438_-207+440delinsCTT
ENST00000697675.1:n.551_553delinsCTT
ENST00000697676.1:n.205+335_205+337delinsCTT
ENST00000697677.1:n.538_540delinsCTT
ENST00000697678.1:n.47+491_47+493delinsCTT
ENST00000697679.1:n.531_533delinsCTT
ENST00000697680.1:c.*321_*323delinsCTT	ENSP00000513392.1:n.*321_*323delinsCTT
ENST00000697681.1:c.*321_*323delinsCTT	ENSP00000513393.1:n.*321_*323delinsCTT
ENST00000697683.1:c.*321_*323delinsCTT	ENSP00000513395.1:n.*321_*323delinsCTT
ENST00000697684.1:n.205+335_205+337delinsCTT
ENST00000697685.1:c.*321_*323delinsCTT	ENSP00000513396.1:n.*321_*323delinsCTT
ENST00000697686.1:c.-207+491_-207+493delinsCTT	ENSP00000513397.1:n.-207+491_-207+493delinsCTT
ENST00000697687.1:n.191+335_191+337delinsCTT
ENST00000697688.1:n.191+335_191+337delinsCTT
ENST00000697689.1:c.*321_*323delinsCTT	ENSP00000513398.1:n.*321_*323delinsCTT
ENST00000697690.1:c.145+335_145+337delinsCTT	ENSP00000513399.1:n.145+335_145+337delinsCTT
ENST00000697691.1:c.43-228_43-226delinsCTT	ENSP00000513400.1:n.43-228_43-226delinsCTT
ENST00000697692.1:c.*157+164_*157+166delinsCTT	ENSP00000513401.1:n.*157+164_*157+166delinsCTT
ENST00000697693.1:n.393_395delinsCTT
ENST00000697694.1:c.-207+5_-207+7delinsCTT	ENSP00000513402.1:n.-207+5_-207+7delinsCTT
ENST00000697695.1:n.197_199delinsCTT
ENST00000337432.9:c.145+335_145+337delinsCTT MANE Select	ENSP00000336701.4:n.145+335_145+337delinsCTT
ENST00000337432.8:c.145+335_145+337delinsCTT	ENSP00000336701.4:n.145+335_145+337delinsCTT
ENST00000421782.3:c.145+335_145+337delinsCTT	ENSP00000391450.2:n.145+335_145+337delinsCTT
ENST00000461271.5:c.-207+438_-207+440delinsCTT	ENSP00000464056.1:n.-207+438_-207+440delinsCTT
ENST00000475762.5:c.*321_*323delinsCTT	ENSP00000432421.1:n.*321_*323delinsCTT
ENST00000476741.2:n.188-228_188-226delinsCTT
ENST00000482007.5:c.145+335_145+337delinsCTT	ENSP00000433332.1:n.145+335_145+337delinsCTT
ENST00000486827.1:c.*321_*323delinsCTT	ENSP00000436761.1:n.*321_*323delinsCTT
ENST00000487525.5:c.145+335_145+337delinsCTT	ENSP00000431637.1:n.145+335_145+337delinsCTT
ENST00000487921.5:n.57+491_57+493delinsCTT
ENST00000583539.5:c.145+335_145+337delinsCTT	ENSP00000463121.1:n.145+335_145+337delinsCTT
ENST00000584617.5:c.126+335_126+337delinsCTT
NM_002876.3:c.145+335_145+337delinsCTT	NP_002867.1:n.145+335_145+337delinsCTT
NM_058216.2:c.145+335_145+337delinsCTT	NP_478123.1:n.145+335_145+337delinsCTT
NR_103872.1:n.216+335_216+337delinsCTT
NR_103873.1:n.113+438_113+440delinsCTT
XM_006722001.2:c.145+335_145+337delinsCTT	XP_006722064.1:n.145+335_145+337delinsCTT
XM_006722002.2:c.145+335_145+337delinsCTT	XP_006722065.1:n.145+335_145+337delinsCTT
XM_006722004.2:c.-207+438_-207+440delinsCTT	XP_006722067.1:n.-207+438_-207+440delinsCTT
XM_006722005.2:c.-207+491_-207+493delinsCTT	XP_006722068.1:n.-207+491_-207+493delinsCTT
XM_011525092.1:c.-506-228_-506-226delinsCTT	XP_011523394.1:n.-506-228_-506-226delinsCTT
XM_011525093.1:c.-667-228_-667-226delinsCTT	XP_011523395.1:n.-667-228_-667-226delinsCTT
XM_011525094.1:c.-207+164_-207+166delinsCTT	XP_011523396.1:n.-207+164_-207+166delinsCTT
XR_934513.1:n.218+335_218+337delinsCTT
XR_934514.1:n.218+335_218+337delinsCTT
XM_006722001.4:c.145+335_145+337delinsCTT	XP_006722064.1:n.145+335_145+337delinsCTT
XM_006722002.4:c.145+335_145+337delinsCTT	XP_006722065.1:n.145+335_145+337delinsCTT
XM_006722004.3:c.-207+438_-207+440delinsCTT	XP_006722067.1:n.-207+438_-207+440delinsCTT
XM_006722005.3:c.-207+491_-207+493delinsCTT	XP_006722068.1:n.-207+491_-207+493delinsCTT
XM_011525092.2:c.-506-228_-506-226delinsCTT	XP_011523394.1:n.-506-228_-506-226delinsCTT
XM_011525093.2:c.-667-228_-667-226delinsCTT	XP_011523395.1:n.-667-228_-667-226delinsCTT
XM_011525094.2:c.-207+164_-207+166delinsCTT	XP_011523396.1:n.-207+164_-207+166delinsCTT
XM_017024914.1:c.-207+438_-207+440delinsCTT	XP_016880403.1:n.-207+438_-207+440delinsCTT
XM_017024916.1:c.-506-228_-506-226delinsCTT	XP_016880405.1:n.-506-228_-506-226delinsCTT
XM_017024917.1:c.-207+491_-207+493delinsCTT	XP_016880406.1:n.-207+491_-207+493delinsCTT
XM_017024918.2:c.-207+164_-207+166delinsCTT	XP_016880407.1:n.-207+164_-207+166delinsCTT
XM_017024919.1:c.-667-228_-667-226delinsCTT	XP_016880408.1:n.-667-228_-667-226delinsCTT
XR_934513.3:n.649+335_649+337delinsCTT
XR_934514.3:n.649+335_649+337delinsCTT
NM_058216.3:c.145+335_145+337delinsCTT MANE Select	NP_478123.1:n.145+335_145+337delinsCTT
NR_103872.2:n.187+335_187+337delinsCTT
NM_002876.4:c.145+335_145+337delinsCTT	NP_002867.1:n.145+335_145+337delinsCTT