Canonical Allele Identifier: CA167675

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 186604
• ClinVar RCV Id: RCV000166223 ; RCV000996589 ; RCV001385150 ; RCV002498821 ; RCV003462204
• dbSNP Id: rs587782286
• gnomAD v4: 17-58703274-CAG-C
• MyVariant Identifiers: chr17:g.56780638_56780639del (hg19) ; chr17:g.56780636_56780637del (hg19) ; chr17:g.58703277_58703278del (hg38) ; chr17:g.58703275_58703276del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703277_58703278del , CM000679.2:g.58703277_58703278del	GRCh38
NC_000017.10:g.56780638_56780639del , CM000679.1:g.56780638_56780639del	GRCh37
NC_000017.9:g.54135637_54135638del	NCBI36
NG_023199.1:g.15676_15677del , LRG_314:g.15676_15677del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.302_303del	ENSP00000464056.2:p.Glu101ValfsTer?
ENST00000697677.1:n.1734_1735del
ENST00000697678.1:n.555_556del
ENST00000697679.1:n.1727_1728del
ENST00000697680.1:c.*1517_*1518del	ENSP00000513392.1:n.*1517_*1518del
ENST00000697681.1:c.*1669_*1670del	ENSP00000513393.1:n.*1669_*1670del
ENST00000697683.1:c.*1517_*1518del	ENSP00000513395.1:n.*1517_*1518del
ENST00000697684.1:n.713_714del
ENST00000697685.1:c.*1350_*1351del	ENSP00000513396.1:n.*1350_*1351del
ENST00000697686.1:c.302_303del	ENSP00000513397.1:p.Glu101ValfsTer?
ENST00000697687.1:n.532_533del
ENST00000697688.1:n.699_700del
ENST00000697689.1:c.*1189_*1190del	ENSP00000513398.1:n.*1189_*1190del
ENST00000697690.1:c.653_654del	ENSP00000513399.1:p.Glu218ValfsTer?
ENST00000697691.1:c.*625_*626del	ENSP00000513400.1:n.*625_*626del
ENST00000697692.1:c.*665_*666del	ENSP00000513401.1:n.*665_*666del
ENST00000697694.1:c.302_303del	ENSP00000513402.1:p.Glu101ValfsTer?
ENST00000697695.1:n.1260_1261del
ENST00000337432.9:c.653_654del MANE Select	ENSP00000336701.4:p.Glu218ValfsTer?
ENST00000337432.8:c.653_654del	ENSP00000336701.4:p.Glu218ValfsTer?
ENST00000413590.5:c.291_292del
ENST00000425173.5:c.449_450del	ENSP00000407282.1:p.Glu150ValfsTer22
ENST00000461271.5:c.302_303del	ENSP00000464056.1:p.Glu101ValfsTer?
ENST00000475762.5:c.*1356_*1357del	ENSP00000432421.1:n.*1356_*1357del
ENST00000482007.5:c.*81_*82del	ENSP00000433332.1:n.*81_*82del
ENST00000487525.5:c.*81_*82del	ENSP00000431637.1:n.*81_*82del
ENST00000487921.5:n.565_566del
ENST00000583539.5:c.653_654del	ENSP00000463121.1:p.Glu218ValfsTer?
ENST00000584617.5:c.375_376del
NM_058216.2:c.653_654del	NP_478123.1:p.Glu218ValfsTer?
NR_103872.1:n.557_558del
XM_006722001.2:c.653_654del	XP_006722064.1:p.Glu218ValfsTer?
XM_006722002.2:c.653_654del	XP_006722065.1:p.Glu218ValfsTer?
XM_006722004.2:c.302_303del	XP_006722067.1:p.Glu101ValfsTer?
XM_006722005.2:c.302_303del	XP_006722068.1:p.Glu101ValfsTer?
XM_011525092.1:c.302_303del	XP_011523394.1:p.Glu101ValfsTer?
XM_011525093.1:c.302_303del	XP_011523395.1:p.Glu101ValfsTer?
XM_011525094.1:c.302_303del	XP_011523396.1:p.Glu101ValfsTer?
XR_934513.1:n.726_727del
XR_934514.1:n.726_727del
XM_006722001.4:c.653_654del	XP_006722064.1:p.Glu218ValfsTer?
XM_006722002.4:c.653_654del	XP_006722065.1:p.Glu218ValfsTer?
XM_006722004.3:c.302_303del	XP_006722067.1:p.Glu101ValfsTer?
XM_006722005.3:c.302_303del	XP_006722068.1:p.Glu101ValfsTer?
XM_011525092.2:c.302_303del	XP_011523394.1:p.Glu101ValfsTer?
XM_011525093.2:c.302_303del	XP_011523395.1:p.Glu101ValfsTer?
XM_011525094.2:c.302_303del	XP_011523396.1:p.Glu101ValfsTer?
XM_017024914.1:c.302_303del	XP_016880403.1:p.Glu101ValfsTer?
XM_017024915.1:c.302_303del	XP_016880404.1:p.Glu101ValfsTer?
XM_017024916.1:c.302_303del	XP_016880405.1:p.Glu101ValfsTer?
XM_017024917.1:c.302_303del	XP_016880406.1:p.Glu101ValfsTer?
XM_017024918.2:c.302_303del	XP_016880407.1:p.Glu101ValfsTer?
XM_017024919.1:c.302_303del	XP_016880408.1:p.Glu101ValfsTer?
XR_934513.3:n.1157_1158del
XR_934514.3:n.1157_1158del
NM_058216.3:c.653_654del MANE Select	NP_478123.1:p.Glu218ValfsTer?
NR_103872.2:n.528_529del