Canonical Allele Identifier: CA2733813154

Gene: RAD51C

Linked Data

• dbSNP Id: rs2143801004

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703304del , CM000679.2:g.58703304del	GRCh38
NC_000017.10:g.56780665del , CM000679.1:g.56780665del	GRCh37
NC_000017.9:g.54135664del	NCBI36
NG_023199.1:g.15703del , LRG_314:g.15703del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.329del	ENSP00000464056.2:p.Pro110GlnfsTer12
ENST00000697677.1:n.1761del
ENST00000697678.1:n.582del
ENST00000697679.1:n.1754del
ENST00000697680.1:c.*1544del	ENSP00000513392.1:n.*1544del
ENST00000697681.1:c.*1696del	ENSP00000513393.1:n.*1696del
ENST00000697683.1:c.*1544del	ENSP00000513395.1:n.*1544del
ENST00000697684.1:n.740del
ENST00000697685.1:c.*1377del	ENSP00000513396.1:n.*1377del
ENST00000697686.1:c.329del	ENSP00000513397.1:p.Pro110GlnfsTer12
ENST00000697687.1:n.559del
ENST00000697688.1:n.726del
ENST00000697689.1:c.*1216del	ENSP00000513398.1:n.*1216del
ENST00000697690.1:c.680del	ENSP00000513399.1:p.Pro227GlnfsTer12
ENST00000697691.1:c.*652del	ENSP00000513400.1:n.*652del
ENST00000697692.1:c.*692del	ENSP00000513401.1:n.*692del
ENST00000697694.1:c.329del	ENSP00000513402.1:p.Pro110GlnfsTer12
ENST00000697695.1:n.1287del
ENST00000337432.9:c.680del MANE Select	ENSP00000336701.4:p.Pro227GlnfsTer12
ENST00000337432.8:c.680del	ENSP00000336701.4:p.Pro227GlnfsTer12
ENST00000413590.5:c.318del
ENST00000425173.5:c.476del	ENSP00000407282.1:p.Pro159GlnfsTer?
ENST00000461271.5:c.329del	ENSP00000464056.1:p.Pro110GlnfsTer12
ENST00000475762.5:c.*1383del	ENSP00000432421.1:n.*1383del
ENST00000482007.5:c.*108del	ENSP00000433332.1:n.*108del
ENST00000487525.5:c.*108del	ENSP00000431637.1:n.*108del
ENST00000487921.5:n.592del
ENST00000583539.5:c.680del	ENSP00000463121.1:p.Pro227GlnfsTer12
ENST00000584617.5:c.402del
NM_058216.2:c.680del	NP_478123.1:p.Pro227GlnfsTer12
NR_103872.1:n.584del
XM_006722001.2:c.680del	XP_006722064.1:p.Pro227GlnfsTer12
XM_006722002.2:c.680del	XP_006722065.1:p.Pro227GlnfsTer12
XM_006722004.2:c.329del	XP_006722067.1:p.Pro110GlnfsTer12
XM_006722005.2:c.329del	XP_006722068.1:p.Pro110GlnfsTer12
XM_011525092.1:c.329del	XP_011523394.1:p.Pro110GlnfsTer12
XM_011525093.1:c.329del	XP_011523395.1:p.Pro110GlnfsTer12
XM_011525094.1:c.329del	XP_011523396.1:p.Pro110GlnfsTer12
XR_934513.1:n.753del
XR_934514.1:n.753del
XM_006722001.4:c.680del	XP_006722064.1:p.Pro227GlnfsTer12
XM_006722002.4:c.680del	XP_006722065.1:p.Pro227GlnfsTer12
XM_006722004.3:c.329del	XP_006722067.1:p.Pro110GlnfsTer12
XM_006722005.3:c.329del	XP_006722068.1:p.Pro110GlnfsTer12
XM_011525092.2:c.329del	XP_011523394.1:p.Pro110GlnfsTer12
XM_011525093.2:c.329del	XP_011523395.1:p.Pro110GlnfsTer12
XM_011525094.2:c.329del	XP_011523396.1:p.Pro110GlnfsTer12
XM_017024914.1:c.329del	XP_016880403.1:p.Pro110GlnfsTer12
XM_017024915.1:c.329del	XP_016880404.1:p.Pro110GlnfsTer12
XM_017024916.1:c.329del	XP_016880405.1:p.Pro110GlnfsTer12
XM_017024917.1:c.329del	XP_016880406.1:p.Pro110GlnfsTer12
XM_017024918.2:c.329del	XP_016880407.1:p.Pro110GlnfsTer12
XM_017024919.1:c.329del	XP_016880408.1:p.Pro110GlnfsTer12
XR_934513.3:n.1184del
XR_934514.3:n.1184del
NM_058216.3:c.680del MANE Select	NP_478123.1:p.Pro227GlnfsTer12
NR_103872.2:n.555del