Canonical Allele Identifier: CA3057228018

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692704_58692705delinsGA , CM000679.2:g.58692704_58692705delinsGA	GRCh38
NC_000017.10:g.56770065_56770066delinsGA , CM000679.1:g.56770065_56770066delinsGA	GRCh37
NC_000017.9:g.54125064_54125065delinsGA	NCBI36
NG_023199.1:g.5103_5104delinsGA , LRG_314:g.5103_5104delinsGA
NG_047169.1:g.4375_4376delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+19_-207+20delinsGA	ENSP00000464056.2:n.-207+19_-207+20delinsGA
ENST00000697675.1:n.132_133delinsGA
ENST00000697676.1:n.121_122delinsGA
ENST00000697677.1:n.119_120delinsGA
ENST00000697678.1:n.47+72_47+73delinsGA
ENST00000697679.1:n.112_113delinsGA
ENST00000697680.1:c.61_62delinsGA	ENSP00000513392.1:p.Pro21Glu
ENST00000697681.1:c.61_62delinsGA	ENSP00000513393.1:p.Pro21Glu
ENST00000697683.1:c.61_62delinsGA	ENSP00000513395.1:p.Pro21Glu
ENST00000697684.1:n.121_122delinsGA
ENST00000697685.1:c.61_62delinsGA	ENSP00000513396.1:p.Pro21Glu
ENST00000697686.1:c.-207+72_-207+73delinsGA	ENSP00000513397.1:n.-207+72_-207+73delinsGA
ENST00000697687.1:n.107_108delinsGA
ENST00000697688.1:n.107_108delinsGA
ENST00000697689.1:c.61_62delinsGA	ENSP00000513398.1:p.Pro21Glu
ENST00000697690.1:c.61_62delinsGA	ENSP00000513399.1:p.Pro21Glu
ENST00000697691.1:c.42+19_42+20delinsGA	ENSP00000513400.1:n.42+19_42+20delinsGA
ENST00000697692.1:c.61_62delinsGA	ENSP00000513401.1:p.Pro21Glu
ENST00000337432.9:c.61_62delinsGA MANE Select	ENSP00000336701.4:p.Pro21Glu
ENST00000337432.8:c.61_62delinsGA	ENSP00000336701.4:p.Pro21Glu
ENST00000421782.3:c.61_62delinsGA	ENSP00000391450.2:p.Pro21Glu
ENST00000461271.5:c.-207+19_-207+20delinsGA	ENSP00000464056.1:n.-207+19_-207+20delinsGA
ENST00000475762.5:c.61_62delinsGA	ENSP00000432421.1:p.Pro21Glu
ENST00000476741.2:n.103_104delinsGA
ENST00000482007.5:c.61_62delinsGA	ENSP00000433332.1:p.Pro21Glu
ENST00000486827.1:c.61_62delinsGA	ENSP00000436761.1:p.Pro21Glu
ENST00000487525.5:c.61_62delinsGA	ENSP00000431637.1:p.Pro21Glu
ENST00000487921.5:n.57+72_57+73delinsGA
ENST00000583539.5:c.61_62delinsGA	ENSP00000463121.1:p.Pro21Glu
ENST00000584617.5:c.42_43delinsGA
NM_002876.3:c.61_62delinsGA	NP_002867.1:p.Pro21Glu
NM_058216.2:c.61_62delinsGA	NP_478123.1:p.Pro21Glu
NR_103872.1:n.132_133delinsGA
NR_103873.1:n.113+19_113+20delinsGA
XM_006722001.2:c.61_62delinsGA	XP_006722064.1:p.Pro21Glu
XM_006722002.2:c.61_62delinsGA	XP_006722065.1:p.Pro21Glu
XM_006722004.2:c.-207+19_-207+20delinsGA	XP_006722067.1:n.-207+19_-207+20delinsGA
XM_006722005.2:c.-207+72_-207+73delinsGA	XP_006722068.1:n.-207+72_-207+73delinsGA
XM_011525092.1:c.-507+19_-507+20delinsGA	XP_011523394.1:n.-507+19_-507+20delinsGA
XM_011525093.1:c.-668+19_-668+20delinsGA	XP_011523395.1:n.-668+19_-668+20delinsGA
XR_934513.1:n.134_135delinsGA
XR_934514.1:n.134_135delinsGA
XM_006722001.4:c.61_62delinsGA	XP_006722064.1:p.Pro21Glu
XM_006722002.4:c.61_62delinsGA	XP_006722065.1:p.Pro21Glu
XM_006722004.3:c.-207+19_-207+20delinsGA	XP_006722067.1:n.-207+19_-207+20delinsGA
XM_006722005.3:c.-207+72_-207+73delinsGA	XP_006722068.1:n.-207+72_-207+73delinsGA
XM_011525092.2:c.-507+19_-507+20delinsGA	XP_011523394.1:n.-507+19_-507+20delinsGA
XM_011525093.2:c.-668+19_-668+20delinsGA	XP_011523395.1:n.-668+19_-668+20delinsGA
XM_017024914.1:c.-207+19_-207+20delinsGA	XP_016880403.1:n.-207+19_-207+20delinsGA
XM_017024916.1:c.-507+19_-507+20delinsGA	XP_016880405.1:n.-507+19_-507+20delinsGA
XM_017024917.1:c.-207+72_-207+73delinsGA	XP_016880406.1:n.-207+72_-207+73delinsGA
XM_017024918.2:c.-462_-461delinsGA	XP_016880407.1:n.-462_-461delinsGA
XM_017024919.1:c.-668+19_-668+20delinsGA	XP_016880408.1:n.-668+19_-668+20delinsGA
XR_934513.3:n.565_566delinsGA
XR_934514.3:n.565_566delinsGA
NM_058216.3:c.61_62delinsGA MANE Select	NP_478123.1:p.Pro21Glu
NR_103872.2:n.103_104delinsGA
NM_002876.4:c.61_62delinsGA	NP_002867.1:p.Pro21Glu