Canonical Allele Identifier: CA2267815218

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58694969_58694971delinsCAA , CM000679.2:g.58694969_58694971delinsCAA	GRCh38
NC_000017.10:g.56772330_56772332delinsCAA , CM000679.1:g.56772330_56772332delinsCAA	GRCh37
NC_000017.9:g.54127329_54127331delinsCAA	NCBI36
NG_023199.1:g.7368_7370delinsCAA , LRG_314:g.7368_7370delinsCAA
NG_047169.1:g.2109_2111delinsTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-168_-166delinsCAA	ENSP00000464056.2:n.-168_-166delinsCAA
ENST00000697675.1:n.1278_1280delinsCAA
ENST00000697676.1:n.244_246delinsCAA
ENST00000697677.1:n.1265_1267delinsCAA
ENST00000697678.1:n.86_88delinsCAA
ENST00000697679.1:n.1258_1260delinsCAA
ENST00000697680.1:c.*1048_*1050delinsCAA	ENSP00000513392.1:n.*1048_*1050delinsCAA
ENST00000697681.1:c.*1048_*1050delinsCAA	ENSP00000513393.1:n.*1048_*1050delinsCAA
ENST00000697683.1:c.*1048_*1050delinsCAA	ENSP00000513395.1:n.*1048_*1050delinsCAA
ENST00000697684.1:n.244_246delinsCAA
ENST00000697685.1:c.*1048_*1050delinsCAA	ENSP00000513396.1:n.*1048_*1050delinsCAA
ENST00000697686.1:c.-168_-166delinsCAA	ENSP00000513397.1:n.-168_-166delinsCAA
ENST00000697687.1:n.230_232delinsCAA
ENST00000697688.1:n.230_232delinsCAA
ENST00000697689.1:c.*887_*889delinsCAA	ENSP00000513398.1:n.*887_*889delinsCAA
ENST00000697690.1:c.184_186delinsCAA	ENSP00000513399.1:p.Gln62=
ENST00000697691.1:c.*156_*158delinsCAA	ENSP00000513400.1:n.*156_*158delinsCAA
ENST00000697692.1:c.*196_*198delinsCAA	ENSP00000513401.1:n.*196_*198delinsCAA
ENST00000697693.1:n.959_961delinsCAA
ENST00000697694.1:c.-168_-166delinsCAA	ENSP00000513402.1:n.-168_-166delinsCAA
ENST00000697695.1:n.791_793delinsCAA
ENST00000337432.9:c.184_186delinsCAA MANE Select	ENSP00000336701.4:p.Gln62=
ENST00000337432.8:c.184_186delinsCAA	ENSP00000336701.4:p.Gln62=
ENST00000421782.3:c.184_186delinsCAA	ENSP00000391450.2:p.Gln62=
ENST00000461271.5:c.-168_-166delinsCAA	ENSP00000464056.1:n.-168_-166delinsCAA
ENST00000475762.5:c.*887_*889delinsCAA	ENSP00000432421.1:n.*887_*889delinsCAA
ENST00000482007.5:c.184_186delinsCAA	ENSP00000433332.1:p.Gln62=
ENST00000486827.1:c.*1048_*1050delinsCAA	ENSP00000436761.1:n.*1048_*1050delinsCAA
ENST00000487525.5:c.184_186delinsCAA	ENSP00000431637.1:p.Gln62=
ENST00000487921.5:n.96_98delinsCAA
ENST00000583539.5:c.184_186delinsCAA	ENSP00000463121.1:p.Gln62=
ENST00000584617.5:c.127-1724_127-1722delinsCAA
NM_002876.3:c.184_186delinsCAA	NP_002867.1:p.Gln62=
NM_058216.2:c.184_186delinsCAA	NP_478123.1:p.Gln62=
NR_103872.1:n.255_257delinsCAA
NR_103873.1:n.152_154delinsCAA
XM_006722001.2:c.184_186delinsCAA	XP_006722064.1:p.Gln62=
XM_006722002.2:c.184_186delinsCAA	XP_006722065.1:p.Gln62=
XM_006722004.2:c.-168_-166delinsCAA	XP_006722067.1:n.-168_-166delinsCAA
XM_006722005.2:c.-168_-166delinsCAA	XP_006722068.1:n.-168_-166delinsCAA
XM_011525092.1:c.-168_-166delinsCAA	XP_011523394.1:n.-168_-166delinsCAA
XM_011525093.1:c.-168_-166delinsCAA	XP_011523395.1:n.-168_-166delinsCAA
XM_011525094.1:c.-168_-166delinsCAA	XP_011523396.1:n.-168_-166delinsCAA
XR_934513.1:n.257_259delinsCAA
XR_934514.1:n.257_259delinsCAA
XM_006722001.4:c.184_186delinsCAA	XP_006722064.1:p.Gln62=
XM_006722002.4:c.184_186delinsCAA	XP_006722065.1:p.Gln62=
XM_006722004.3:c.-168_-166delinsCAA	XP_006722067.1:n.-168_-166delinsCAA
XM_006722005.3:c.-168_-166delinsCAA	XP_006722068.1:n.-168_-166delinsCAA
XM_011525092.2:c.-168_-166delinsCAA	XP_011523394.1:n.-168_-166delinsCAA
XM_011525093.2:c.-168_-166delinsCAA	XP_011523395.1:n.-168_-166delinsCAA
XM_011525094.2:c.-168_-166delinsCAA	XP_011523396.1:n.-168_-166delinsCAA
XM_017024914.1:c.-168_-166delinsCAA	XP_016880403.1:n.-168_-166delinsCAA
XM_017024915.1:c.-168_-166delinsCAA	XP_016880404.1:n.-168_-166delinsCAA
XM_017024916.1:c.-168_-166delinsCAA	XP_016880405.1:n.-168_-166delinsCAA
XM_017024917.1:c.-168_-166delinsCAA	XP_016880406.1:n.-168_-166delinsCAA
XM_017024918.2:c.-168_-166delinsCAA	XP_016880407.1:n.-168_-166delinsCAA
XM_017024919.1:c.-168_-166delinsCAA	XP_016880408.1:n.-168_-166delinsCAA
XR_934513.3:n.688_690delinsCAA
XR_934514.3:n.688_690delinsCAA
NM_058216.3:c.184_186delinsCAA MANE Select	NP_478123.1:p.Gln62=
NR_103872.2:n.226_228delinsCAA
NM_002876.4:c.184_186delinsCAA	NP_002867.1:p.Gln62=