Canonical Allele Identifier: CA3057228000

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692643_58692645delinsTGA , CM000679.2:g.58692643_58692645delinsTGA	GRCh38
NC_000017.10:g.56770004_56770006delinsTGA , CM000679.1:g.56770004_56770006delinsTGA	GRCh37
NC_000017.9:g.54125003_54125005delinsTGA	NCBI36
NG_023199.1:g.5042_5044delinsTGA , LRG_314:g.5042_5044delinsTGA
NG_047169.1:g.4435_4437delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-249_-247delinsTGA	ENSP00000464056.2:n.-249_-247delinsTGA
ENST00000697675.1:n.71_73delinsTGA
ENST00000697676.1:n.60_62delinsTGA
ENST00000697677.1:n.58_60delinsTGA
ENST00000697678.1:n.47+11_47+13delinsTGA
ENST00000697679.1:n.51_53delinsTGA
ENST00000697680.1:c.-1_2delinsTGA
ENST00000697681.1:c.-1_2delinsTGA
ENST00000697683.1:c.-1_2delinsTGA
ENST00000697684.1:n.60_62delinsTGA
ENST00000697685.1:c.-1_2delinsTGA
ENST00000697686.1:c.-207+11_-207+13delinsTGA	ENSP00000513397.1:n.-207+11_-207+13delinsTGA
ENST00000697687.1:n.46_48delinsTGA
ENST00000697688.1:n.46_48delinsTGA
ENST00000697689.1:c.-1_2delinsTGA
ENST00000697690.1:c.-1_2delinsTGA
ENST00000697691.1:c.-1_2delinsTGA
ENST00000697692.1:c.-1_2delinsTGA
ENST00000337432.9:c.-1_2delinsTGA
ENST00000337432.8:c.-1_2delinsTGA
ENST00000421782.3:c.-1_2delinsTGA
ENST00000461271.5:c.-249_-247delinsTGA	ENSP00000464056.1:n.-249_-247delinsTGA
ENST00000475762.5:c.-1_2delinsTGA
ENST00000476741.2:n.42_44delinsTGA
ENST00000482007.5:c.-1_2delinsTGA
ENST00000486827.1:c.-1_2delinsTGA
ENST00000487525.5:c.-1_2delinsTGA
ENST00000487921.5:n.57+11_57+13delinsTGA
ENST00000583539.5:c.-1_2delinsTGA
NM_002876.3:c.-1_2delinsTGA
NM_058216.2:c.-1_2delinsTGA
NR_103872.1:n.71_73delinsTGA
NR_103873.1:n.71_73delinsTGA
XM_006722001.2:c.-1_2delinsTGA
XM_006722002.2:c.-1_2delinsTGA
XM_006722004.2:c.-249_-247delinsTGA	XP_006722067.1:n.-249_-247delinsTGA
XM_006722005.2:c.-207+11_-207+13delinsTGA	XP_006722068.1:n.-207+11_-207+13delinsTGA
XM_011525092.1:c.-549_-547delinsTGA	XP_011523394.1:n.-549_-547delinsTGA
XM_011525093.1:c.-710_-708delinsTGA	XP_011523395.1:n.-710_-708delinsTGA
XR_934513.1:n.73_75delinsTGA
XR_934514.1:n.73_75delinsTGA
XM_006722001.4:c.-1_2delinsTGA
XM_006722002.4:c.-1_2delinsTGA
XM_006722004.3:c.-249_-247delinsTGA	XP_006722067.1:n.-249_-247delinsTGA
XM_006722005.3:c.-207+11_-207+13delinsTGA	XP_006722068.1:n.-207+11_-207+13delinsTGA
XM_017024914.1:c.-249_-247delinsTGA	XP_016880403.1:n.-249_-247delinsTGA
XM_017024916.1:c.-549_-547delinsTGA	XP_016880405.1:n.-549_-547delinsTGA
XM_017024917.1:c.-207+11_-207+13delinsTGA	XP_016880406.1:n.-207+11_-207+13delinsTGA
XM_017024918.2:c.-523_-521delinsTGA	XP_016880407.1:n.-523_-521delinsTGA
XR_934513.3:n.504_506delinsTGA
XR_934514.3:n.504_506delinsTGA
NM_058216.3:c.-1_2delinsTGA
NR_103872.2:n.42_44delinsTGA
NM_002876.4:c.-1_2delinsTGA