Canonical Allele Identifier: CA2267814275

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58693060_58693063delinsTTAC , CM000679.2:g.58693060_58693063delinsTTAC	GRCh38
NC_000017.10:g.56770421_56770424delinsTTAC , CM000679.1:g.56770421_56770424delinsTTAC	GRCh37
NC_000017.9:g.54125420_54125423delinsTTAC	NCBI36
NG_023199.1:g.5459_5462delinsTTAC , LRG_314:g.5459_5462delinsTTAC
NG_047169.1:g.4017_4020delinsGTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+375_-207+378delinsTTAC	ENSP00000464056.2:n.-207+375_-207+378delinsTTAC
ENST00000697675.1:n.488_491delinsTTAC
ENST00000697676.1:n.205+272_205+275delinsTTAC
ENST00000697677.1:n.475_478delinsTTAC
ENST00000697678.1:n.47+428_47+431delinsTTAC
ENST00000697679.1:n.468_471delinsTTAC
ENST00000697680.1:c.*258_*261delinsTTAC	ENSP00000513392.1:n.*258_*261delinsTTAC
ENST00000697681.1:c.*258_*261delinsTTAC	ENSP00000513393.1:n.*258_*261delinsTTAC
ENST00000697683.1:c.*258_*261delinsTTAC	ENSP00000513395.1:n.*258_*261delinsTTAC
ENST00000697684.1:n.205+272_205+275delinsTTAC
ENST00000697685.1:c.*258_*261delinsTTAC	ENSP00000513396.1:n.*258_*261delinsTTAC
ENST00000697686.1:c.-207+428_-207+431delinsTTAC	ENSP00000513397.1:n.-207+428_-207+431delinsTTAC
ENST00000697687.1:n.191+272_191+275delinsTTAC
ENST00000697688.1:n.191+272_191+275delinsTTAC
ENST00000697689.1:c.*258_*261delinsTTAC	ENSP00000513398.1:n.*258_*261delinsTTAC
ENST00000697690.1:c.145+272_145+275delinsTTAC	ENSP00000513399.1:n.145+272_145+275delinsTTAC
ENST00000697691.1:c.43-291_43-288delinsTTAC	ENSP00000513400.1:n.43-291_43-288delinsTTAC
ENST00000697692.1:c.*157+101_*157+104delinsTTAC	ENSP00000513401.1:n.*157+101_*157+104delinsTTAC
ENST00000697693.1:n.330_333delinsTTAC
ENST00000697694.1:c.-265_-262delinsTTAC	ENSP00000513402.1:n.-265_-262delinsTTAC
ENST00000697695.1:n.134_137delinsTTAC
ENST00000337432.9:c.145+272_145+275delinsTTAC MANE Select	ENSP00000336701.4:n.145+272_145+275delinsTTAC
ENST00000337432.8:c.145+272_145+275delinsTTAC	ENSP00000336701.4:n.145+272_145+275delinsTTAC
ENST00000421782.3:c.145+272_145+275delinsTTAC	ENSP00000391450.2:n.145+272_145+275delinsTTAC
ENST00000461271.5:c.-207+375_-207+378delinsTTAC	ENSP00000464056.1:n.-207+375_-207+378delinsTTAC
ENST00000475762.5:c.*258_*261delinsTTAC	ENSP00000432421.1:n.*258_*261delinsTTAC
ENST00000476741.2:n.187+272_187+275delinsTTAC
ENST00000482007.5:c.145+272_145+275delinsTTAC	ENSP00000433332.1:n.145+272_145+275delinsTTAC
ENST00000486827.1:c.*258_*261delinsTTAC	ENSP00000436761.1:n.*258_*261delinsTTAC
ENST00000487525.5:c.145+272_145+275delinsTTAC	ENSP00000431637.1:n.145+272_145+275delinsTTAC
ENST00000487921.5:n.57+428_57+431delinsTTAC
ENST00000583539.5:c.145+272_145+275delinsTTAC	ENSP00000463121.1:n.145+272_145+275delinsTTAC
ENST00000584617.5:c.126+272_126+275delinsTTAC
NM_002876.3:c.145+272_145+275delinsTTAC	NP_002867.1:n.145+272_145+275delinsTTAC
NM_058216.2:c.145+272_145+275delinsTTAC	NP_478123.1:n.145+272_145+275delinsTTAC
NR_103872.1:n.216+272_216+275delinsTTAC
NR_103873.1:n.113+375_113+378delinsTTAC
XM_006722001.2:c.145+272_145+275delinsTTAC	XP_006722064.1:n.145+272_145+275delinsTTAC
XM_006722002.2:c.145+272_145+275delinsTTAC	XP_006722065.1:n.145+272_145+275delinsTTAC
XM_006722004.2:c.-207+375_-207+378delinsTTAC	XP_006722067.1:n.-207+375_-207+378delinsTTAC
XM_006722005.2:c.-207+428_-207+431delinsTTAC	XP_006722068.1:n.-207+428_-207+431delinsTTAC
XM_011525092.1:c.-506-291_-506-288delinsTTAC	XP_011523394.1:n.-506-291_-506-288delinsTTAC
XM_011525093.1:c.-667-291_-667-288delinsTTAC	XP_011523395.1:n.-667-291_-667-288delinsTTAC
XM_011525094.1:c.-207+101_-207+104delinsTTAC	XP_011523396.1:n.-207+101_-207+104delinsTTAC
XR_934513.1:n.218+272_218+275delinsTTAC
XR_934514.1:n.218+272_218+275delinsTTAC
XM_006722001.4:c.145+272_145+275delinsTTAC	XP_006722064.1:n.145+272_145+275delinsTTAC
XM_006722002.4:c.145+272_145+275delinsTTAC	XP_006722065.1:n.145+272_145+275delinsTTAC
XM_006722004.3:c.-207+375_-207+378delinsTTAC	XP_006722067.1:n.-207+375_-207+378delinsTTAC
XM_006722005.3:c.-207+428_-207+431delinsTTAC	XP_006722068.1:n.-207+428_-207+431delinsTTAC
XM_011525092.2:c.-506-291_-506-288delinsTTAC	XP_011523394.1:n.-506-291_-506-288delinsTTAC
XM_011525093.2:c.-667-291_-667-288delinsTTAC	XP_011523395.1:n.-667-291_-667-288delinsTTAC
XM_011525094.2:c.-207+101_-207+104delinsTTAC	XP_011523396.1:n.-207+101_-207+104delinsTTAC
XM_017024914.1:c.-207+375_-207+378delinsTTAC	XP_016880403.1:n.-207+375_-207+378delinsTTAC
XM_017024916.1:c.-506-291_-506-288delinsTTAC	XP_016880405.1:n.-506-291_-506-288delinsTTAC
XM_017024917.1:c.-207+428_-207+431delinsTTAC	XP_016880406.1:n.-207+428_-207+431delinsTTAC
XM_017024918.2:c.-207+101_-207+104delinsTTAC	XP_016880407.1:n.-207+101_-207+104delinsTTAC
XM_017024919.1:c.-667-291_-667-288delinsTTAC	XP_016880408.1:n.-667-291_-667-288delinsTTAC
XR_934513.3:n.649+272_649+275delinsTTAC
XR_934514.3:n.649+272_649+275delinsTTAC
NM_058216.3:c.145+272_145+275delinsTTAC MANE Select	NP_478123.1:n.145+272_145+275delinsTTAC
NR_103872.2:n.187+272_187+275delinsTTAC
NM_002876.4:c.145+272_145+275delinsTTAC	NP_002867.1:n.145+272_145+275delinsTTAC