Canonical Allele Identifier: CA2639015944

Gene: RAD51C

Linked Data

• gnomAD v4: 17-58703311-CCTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703313_58703316del , CM000679.2:g.58703313_58703316del	GRCh38
NC_000017.10:g.56780674_56780677del , CM000679.1:g.56780674_56780677del	GRCh37
NC_000017.9:g.54135673_54135676del	NCBI36
NG_023199.1:g.15712_15715del , LRG_314:g.15712_15715del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.338_341del	ENSP00000464056.2:p.Leu113GlnfsTer8
ENST00000697677.1:n.1770_1773del
ENST00000697678.1:n.591_594del
ENST00000697679.1:n.1763_1766del
ENST00000697680.1:c.*1553_*1556del	ENSP00000513392.1:n.*1553_*1556del
ENST00000697681.1:c.*1705_*1708del	ENSP00000513393.1:n.*1705_*1708del
ENST00000697683.1:c.*1553_*1556del	ENSP00000513395.1:n.*1553_*1556del
ENST00000697684.1:n.749_752del
ENST00000697685.1:c.*1386_*1389del	ENSP00000513396.1:n.*1386_*1389del
ENST00000697686.1:c.338_341del	ENSP00000513397.1:p.Leu113GlnfsTer8
ENST00000697687.1:n.568_571del
ENST00000697688.1:n.735_738del
ENST00000697689.1:c.*1225_*1228del	ENSP00000513398.1:n.*1225_*1228del
ENST00000697690.1:c.689_692del	ENSP00000513399.1:p.Leu230GlnfsTer8
ENST00000697691.1:c.*661_*664del	ENSP00000513400.1:n.*661_*664del
ENST00000697692.1:c.*701_*704del	ENSP00000513401.1:n.*701_*704del
ENST00000697694.1:c.338_341del	ENSP00000513402.1:p.Leu113GlnfsTer8
ENST00000697695.1:n.1296_1299del
ENST00000337432.9:c.689_692del MANE Select	ENSP00000336701.4:p.Leu230GlnfsTer8
ENST00000337432.8:c.689_692del	ENSP00000336701.4:p.Leu230GlnfsTer8
ENST00000413590.5:c.327_330del
ENST00000425173.5:c.485_488del	ENSP00000407282.1:p.Leu162GlnfsTer?
ENST00000461271.5:c.338_341del	ENSP00000464056.1:p.Leu113GlnfsTer8
ENST00000475762.5:c.*1392_*1395del	ENSP00000432421.1:n.*1392_*1395del
ENST00000482007.5:c.*117_*120del	ENSP00000433332.1:n.*117_*120del
ENST00000487525.5:c.*117_*120del	ENSP00000431637.1:n.*117_*120del
ENST00000487921.5:n.601_604del
ENST00000583539.5:c.689_692del	ENSP00000463121.1:p.Leu230GlnfsTer8
ENST00000584617.5:c.411_414del
NM_058216.2:c.689_692del	NP_478123.1:p.Leu230GlnfsTer8
NR_103872.1:n.593_596del
XM_006722001.2:c.689_692del	XP_006722064.1:p.Leu230GlnfsTer8
XM_006722002.2:c.689_692del	XP_006722065.1:p.Leu230GlnfsTer8
XM_006722004.2:c.338_341del	XP_006722067.1:p.Leu113GlnfsTer8
XM_006722005.2:c.338_341del	XP_006722068.1:p.Leu113GlnfsTer8
XM_011525092.1:c.338_341del	XP_011523394.1:p.Leu113GlnfsTer8
XM_011525093.1:c.338_341del	XP_011523395.1:p.Leu113GlnfsTer8
XM_011525094.1:c.338_341del	XP_011523396.1:p.Leu113GlnfsTer8
XR_934513.1:n.762_765del
XR_934514.1:n.762_765del
XM_006722001.4:c.689_692del	XP_006722064.1:p.Leu230GlnfsTer8
XM_006722002.4:c.689_692del	XP_006722065.1:p.Leu230GlnfsTer8
XM_006722004.3:c.338_341del	XP_006722067.1:p.Leu113GlnfsTer8
XM_006722005.3:c.338_341del	XP_006722068.1:p.Leu113GlnfsTer8
XM_011525092.2:c.338_341del	XP_011523394.1:p.Leu113GlnfsTer8
XM_011525093.2:c.338_341del	XP_011523395.1:p.Leu113GlnfsTer8
XM_011525094.2:c.338_341del	XP_011523396.1:p.Leu113GlnfsTer8
XM_017024914.1:c.338_341del	XP_016880403.1:p.Leu113GlnfsTer8
XM_017024915.1:c.338_341del	XP_016880404.1:p.Leu113GlnfsTer8
XM_017024916.1:c.338_341del	XP_016880405.1:p.Leu113GlnfsTer8
XM_017024917.1:c.338_341del	XP_016880406.1:p.Leu113GlnfsTer8
XM_017024918.2:c.338_341del	XP_016880407.1:p.Leu113GlnfsTer8
XM_017024919.1:c.338_341del	XP_016880408.1:p.Leu113GlnfsTer8
XR_934513.3:n.1193_1196del
XR_934514.3:n.1193_1196del
NM_058216.3:c.689_692del MANE Select	NP_478123.1:p.Leu230GlnfsTer8
NR_103872.2:n.564_567del