Canonical Allele Identifier: CA2639016734

Gene: RAD51C

Linked Data

• gnomAD v4: 17-58709761-AAGAGAGAAGGTCCCTGCTCTCTTGGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709769_58709795del , CM000679.2:g.58709769_58709795del	GRCh38
NC_000017.10:g.56787130_56787156del , CM000679.1:g.56787130_56787156del	GRCh37
NC_000017.9:g.54142129_54142155del	NCBI36
NG_023199.1:g.22168_22194del , LRG_314:g.22168_22194del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.355-90_355-64del	ENSP00000464056.2:n.355-90_355-64del
ENST00000697678.1:n.608-90_608-64del
ENST00000697679.1:n.1780-90_1780-64del
ENST00000697680.1:c.*1570-90_*1570-64del	ENSP00000513392.1:n.*1570-90_*1570-64del
ENST00000697681.1:c.*1867-90_*1867-64del	ENSP00000513393.1:n.*1867-90_*1867-64del
ENST00000697683.1:c.*1570-90_*1570-64del	ENSP00000513395.1:n.*1570-90_*1570-64del
ENST00000697684.1:n.766-90_766-64del
ENST00000697685.1:c.*1403-90_*1403-64del	ENSP00000513396.1:n.*1403-90_*1403-64del
ENST00000697686.1:c.355-90_355-64del	ENSP00000513397.1:n.355-90_355-64del
ENST00000697687.1:n.585-90_585-64del
ENST00000697688.1:n.752-90_752-64del
ENST00000697689.1:c.*1242-90_*1242-64del	ENSP00000513398.1:n.*1242-90_*1242-64del
ENST00000697690.1:c.706-90_706-64del	ENSP00000513399.1:n.706-90_706-64del
ENST00000697691.1:c.*678-90_*678-64del	ENSP00000513400.1:n.*678-90_*678-64del
ENST00000697692.1:c.*718-90_*718-64del	ENSP00000513401.1:n.*718-90_*718-64del
ENST00000697694.1:c.355-90_355-64del	ENSP00000513402.1:n.355-90_355-64del
ENST00000697695.1:n.1313-90_1313-64del
ENST00000337432.9:c.706-90_706-64del MANE Select	ENSP00000336701.4:n.706-90_706-64del
ENST00000337432.8:c.706-90_706-64del	ENSP00000336701.4:n.706-90_706-64del
ENST00000413590.5:c.344-90_344-64del
ENST00000425173.5:c.622-90_622-64del	ENSP00000407282.1:n.622-90_622-64del
ENST00000461271.5:c.355-90_355-64del	ENSP00000464056.1:n.355-90_355-64del
ENST00000475762.5:c.*1409-90_*1409-64del	ENSP00000432421.1:n.*1409-90_*1409-64del
ENST00000482007.5:c.*134-90_*134-64del	ENSP00000433332.1:n.*134-90_*134-64del
ENST00000487525.5:c.*279-90_*279-64del	ENSP00000431637.1:n.*279-90_*279-64del
ENST00000581221.5:n.131_157del
ENST00000583539.5:c.706-90_706-64del	ENSP00000463121.1:n.706-90_706-64del
ENST00000584617.5:c.428-90_428-64del
NM_058216.2:c.706-90_706-64del	NP_478123.1:n.706-90_706-64del
NR_103872.1:n.610-90_610-64del
XM_006722001.2:c.706-90_706-64del	XP_006722064.1:n.706-90_706-64del
XM_006722002.2:c.706-90_706-64del	XP_006722065.1:n.706-90_706-64del
XM_006722004.2:c.355-90_355-64del	XP_006722067.1:n.355-90_355-64del
XM_006722005.2:c.355-90_355-64del	XP_006722068.1:n.355-90_355-64del
XM_011525092.1:c.355-90_355-64del	XP_011523394.1:n.355-90_355-64del
XM_011525093.1:c.355-90_355-64del	XP_011523395.1:n.355-90_355-64del
XM_011525094.1:c.355-90_355-64del	XP_011523396.1:n.355-90_355-64del
XR_934513.1:n.924-90_924-64del
XR_934514.1:n.924-90_924-64del
XM_006722001.4:c.706-90_706-64del	XP_006722064.1:n.706-90_706-64del
XM_006722002.4:c.706-90_706-64del	XP_006722065.1:n.706-90_706-64del
XM_006722004.3:c.355-90_355-64del	XP_006722067.1:n.355-90_355-64del
XM_006722005.3:c.355-90_355-64del	XP_006722068.1:n.355-90_355-64del
XM_011525092.2:c.355-90_355-64del	XP_011523394.1:n.355-90_355-64del
XM_011525093.2:c.355-90_355-64del	XP_011523395.1:n.355-90_355-64del
XM_011525094.2:c.355-90_355-64del	XP_011523396.1:n.355-90_355-64del
XM_017024914.1:c.355-90_355-64del	XP_016880403.1:n.355-90_355-64del
XM_017024915.1:c.355-90_355-64del	XP_016880404.1:n.355-90_355-64del
XM_017024916.1:c.355-90_355-64del	XP_016880405.1:n.355-90_355-64del
XM_017024917.1:c.355-90_355-64del	XP_016880406.1:n.355-90_355-64del
XM_017024918.2:c.355-90_355-64del	XP_016880407.1:n.355-90_355-64del
XM_017024919.1:c.355-90_355-64del	XP_016880408.1:n.355-90_355-64del
XR_934513.3:n.1355-90_1355-64del
XR_934514.3:n.1355-90_1355-64del
NM_058216.3:c.706-90_706-64del MANE Select	NP_478123.1:n.706-90_706-64del
NR_103872.2:n.581-90_581-64del