Canonical Allele Identifier: CA2267814140

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692846_58692847delinsCT , CM000679.2:g.58692846_58692847delinsCT	GRCh38
NC_000017.10:g.56770207_56770208delinsCT , CM000679.1:g.56770207_56770208delinsCT	GRCh37
NC_000017.9:g.54125206_54125207delinsCT	NCBI36
NG_023199.1:g.5245_5246delinsCT , LRG_314:g.5245_5246delinsCT
NG_047169.1:g.4233_4234delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+161_-207+162delinsCT	ENSP00000464056.2:n.-207+161_-207+162delinsCT
ENST00000697675.1:n.274_275delinsCT
ENST00000697676.1:n.205+58_205+59delinsCT
ENST00000697677.1:n.261_262delinsCT
ENST00000697678.1:n.47+214_47+215delinsCT
ENST00000697679.1:n.254_255delinsCT
ENST00000697680.1:c.*44_*45delinsCT	ENSP00000513392.1:n.*44_*45delinsCT
ENST00000697681.1:c.*44_*45delinsCT	ENSP00000513393.1:n.*44_*45delinsCT
ENST00000697683.1:c.*44_*45delinsCT	ENSP00000513395.1:n.*44_*45delinsCT
ENST00000697684.1:n.205+58_205+59delinsCT
ENST00000697685.1:c.*44_*45delinsCT	ENSP00000513396.1:n.*44_*45delinsCT
ENST00000697686.1:c.-207+214_-207+215delinsCT	ENSP00000513397.1:n.-207+214_-207+215delinsCT
ENST00000697687.1:n.191+58_191+59delinsCT
ENST00000697688.1:n.191+58_191+59delinsCT
ENST00000697689.1:c.*44_*45delinsCT	ENSP00000513398.1:n.*44_*45delinsCT
ENST00000697690.1:c.145+58_145+59delinsCT	ENSP00000513399.1:n.145+58_145+59delinsCT
ENST00000697691.1:c.42+161_42+162delinsCT	ENSP00000513400.1:n.42+161_42+162delinsCT
ENST00000697692.1:c.*44_*45delinsCT	ENSP00000513401.1:n.*44_*45delinsCT
ENST00000697693.1:n.116_117delinsCT
ENST00000337432.9:c.145+58_145+59delinsCT MANE Select	ENSP00000336701.4:n.145+58_145+59delinsCT
ENST00000337432.8:c.145+58_145+59delinsCT	ENSP00000336701.4:n.145+58_145+59delinsCT
ENST00000421782.3:c.145+58_145+59delinsCT	ENSP00000391450.2:n.145+58_145+59delinsCT
ENST00000461271.5:c.-207+161_-207+162delinsCT	ENSP00000464056.1:n.-207+161_-207+162delinsCT
ENST00000475762.5:c.*44_*45delinsCT	ENSP00000432421.1:n.*44_*45delinsCT
ENST00000476741.2:n.187+58_187+59delinsCT
ENST00000482007.5:c.145+58_145+59delinsCT	ENSP00000433332.1:n.145+58_145+59delinsCT
ENST00000486827.1:c.*44_*45delinsCT	ENSP00000436761.1:n.*44_*45delinsCT
ENST00000487525.5:c.145+58_145+59delinsCT	ENSP00000431637.1:n.145+58_145+59delinsCT
ENST00000487921.5:n.57+214_57+215delinsCT
ENST00000583539.5:c.145+58_145+59delinsCT	ENSP00000463121.1:n.145+58_145+59delinsCT
ENST00000584617.5:c.126+58_126+59delinsCT
NM_002876.3:c.145+58_145+59delinsCT	NP_002867.1:n.145+58_145+59delinsCT
NM_058216.2:c.145+58_145+59delinsCT	NP_478123.1:n.145+58_145+59delinsCT
NR_103872.1:n.216+58_216+59delinsCT
NR_103873.1:n.113+161_113+162delinsCT
XM_006722001.2:c.145+58_145+59delinsCT	XP_006722064.1:n.145+58_145+59delinsCT
XM_006722002.2:c.145+58_145+59delinsCT	XP_006722065.1:n.145+58_145+59delinsCT
XM_006722004.2:c.-207+161_-207+162delinsCT	XP_006722067.1:n.-207+161_-207+162delinsCT
XM_006722005.2:c.-207+214_-207+215delinsCT	XP_006722068.1:n.-207+214_-207+215delinsCT
XM_011525092.1:c.-507+161_-507+162delinsCT	XP_011523394.1:n.-507+161_-507+162delinsCT
XM_011525093.1:c.-668+161_-668+162delinsCT	XP_011523395.1:n.-668+161_-668+162delinsCT
XM_011525094.1:c.-320_-319delinsCT	XP_011523396.1:n.-320_-319delinsCT
XR_934513.1:n.218+58_218+59delinsCT
XR_934514.1:n.218+58_218+59delinsCT
XM_006722001.4:c.145+58_145+59delinsCT	XP_006722064.1:n.145+58_145+59delinsCT
XM_006722002.4:c.145+58_145+59delinsCT	XP_006722065.1:n.145+58_145+59delinsCT
XM_006722004.3:c.-207+161_-207+162delinsCT	XP_006722067.1:n.-207+161_-207+162delinsCT
XM_006722005.3:c.-207+214_-207+215delinsCT	XP_006722068.1:n.-207+214_-207+215delinsCT
XM_011525092.2:c.-507+161_-507+162delinsCT	XP_011523394.1:n.-507+161_-507+162delinsCT
XM_011525093.2:c.-668+161_-668+162delinsCT	XP_011523395.1:n.-668+161_-668+162delinsCT
XM_011525094.2:c.-320_-319delinsCT	XP_011523396.1:n.-320_-319delinsCT
XM_017024914.1:c.-207+161_-207+162delinsCT	XP_016880403.1:n.-207+161_-207+162delinsCT
XM_017024916.1:c.-507+161_-507+162delinsCT	XP_016880405.1:n.-507+161_-507+162delinsCT
XM_017024917.1:c.-207+214_-207+215delinsCT	XP_016880406.1:n.-207+214_-207+215delinsCT
XM_017024918.2:c.-320_-319delinsCT	XP_016880407.1:n.-320_-319delinsCT
XM_017024919.1:c.-668+161_-668+162delinsCT	XP_016880408.1:n.-668+161_-668+162delinsCT
XR_934513.3:n.649+58_649+59delinsCT
XR_934514.3:n.649+58_649+59delinsCT
NM_058216.3:c.145+58_145+59delinsCT MANE Select	NP_478123.1:n.145+58_145+59delinsCT
NR_103872.2:n.187+58_187+59delinsCT
NM_002876.4:c.145+58_145+59delinsCT	NP_002867.1:n.145+58_145+59delinsCT