Canonical Allele Identifier: CA658658639

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 480492
• ClinVar RCV Id: RCV000569360 ; RCV000802080
• dbSNP Id: rs1555593808
• MyVariant Identifiers: chr17:g.56772507_56772509del (hg19) ; chr17:g.58695146_58695148del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695146_58695148del , CM000679.2:g.58695146_58695148del	GRCh38
NC_000017.10:g.56772507_56772509del , CM000679.1:g.56772507_56772509del	GRCh37
NC_000017.9:g.54127506_54127508del	NCBI36
NG_023199.1:g.7545_7547del , LRG_314:g.7545_7547del
NG_047169.1:g.1936_1938del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.10_12del	ENSP00000464056.2:p.Thr4del
ENST00000697675.1:n.1455_1457del
ENST00000697676.1:n.421_423del
ENST00000697677.1:n.1442_1444del
ENST00000697678.1:n.263_265del
ENST00000697679.1:n.1435_1437del
ENST00000697680.1:c.*1225_*1227del	ENSP00000513392.1:n.*1225_*1227del
ENST00000697681.1:c.*1225_*1227del	ENSP00000513393.1:n.*1225_*1227del
ENST00000697683.1:c.*1225_*1227del	ENSP00000513395.1:n.*1225_*1227del
ENST00000697684.1:n.421_423del
ENST00000697685.1:c.*1225_*1227del	ENSP00000513396.1:n.*1225_*1227del
ENST00000697686.1:c.10_12del	ENSP00000513397.1:p.Thr4del
ENST00000697687.1:n.407_409del
ENST00000697688.1:n.407_409del
ENST00000697689.1:c.*1064_*1066del	ENSP00000513398.1:n.*1064_*1066del
ENST00000697690.1:c.361_363del	ENSP00000513399.1:p.Thr121del
ENST00000697691.1:c.*333_*335del	ENSP00000513400.1:n.*333_*335del
ENST00000697692.1:c.*373_*375del	ENSP00000513401.1:n.*373_*375del
ENST00000697693.1:n.1136_1138del
ENST00000697694.1:c.10_12del	ENSP00000513402.1:p.Thr4del
ENST00000697695.1:n.968_970del
ENST00000337432.9:c.361_363del MANE Select	ENSP00000336701.4:p.Thr121del
ENST00000337432.8:c.361_363del	ENSP00000336701.4:p.Thr121del
ENST00000421782.3:c.361_363del	ENSP00000391450.2:p.Thr121del
ENST00000425173.5:c.157_159del	ENSP00000407282.1:p.Thr53del
ENST00000461271.5:c.10_12del	ENSP00000464056.1:p.Thr4del
ENST00000475762.5:c.*1064_*1066del	ENSP00000432421.1:n.*1064_*1066del
ENST00000482007.5:c.361_363del	ENSP00000433332.1:p.Thr121del
ENST00000486827.1:c.*1225_*1227del	ENSP00000436761.1:n.*1225_*1227del
ENST00000487525.5:c.361_363del	ENSP00000431637.1:p.Thr121del
ENST00000487921.5:n.273_275del
ENST00000583539.5:c.361_363del	ENSP00000463121.1:p.Thr121del
ENST00000584617.5:c.127-1547_127-1545del
ENST00000622327.4:c.97_99del	ENSP00000482326.1:p.Thr33del
NM_002876.3:c.361_363del	NP_002867.1:p.Thr121del
NM_058216.2:c.361_363del	NP_478123.1:p.Thr121del
NR_103872.1:n.432_434del
NR_103873.1:n.329_331del
XM_006722001.2:c.361_363del	XP_006722064.1:p.Thr121del
XM_006722002.2:c.361_363del	XP_006722065.1:p.Thr121del
XM_006722004.2:c.10_12del	XP_006722067.1:p.Thr4del
XM_006722005.2:c.10_12del	XP_006722068.1:p.Thr4del
XM_011525092.1:c.10_12del	XP_011523394.1:p.Thr4del
XM_011525093.1:c.10_12del	XP_011523395.1:p.Thr4del
XM_011525094.1:c.10_12del	XP_011523396.1:p.Thr4del
XR_934513.1:n.434_436del
XR_934514.1:n.434_436del
XM_006722001.4:c.361_363del	XP_006722064.1:p.Thr121del
XM_006722002.4:c.361_363del	XP_006722065.1:p.Thr121del
XM_006722004.3:c.10_12del	XP_006722067.1:p.Thr4del
XM_006722005.3:c.10_12del	XP_006722068.1:p.Thr4del
XM_011525092.2:c.10_12del	XP_011523394.1:p.Thr4del
XM_011525093.2:c.10_12del	XP_011523395.1:p.Thr4del
XM_011525094.2:c.10_12del	XP_011523396.1:p.Thr4del
XM_017024914.1:c.10_12del	XP_016880403.1:p.Thr4del
XM_017024915.1:c.10_12del	XP_016880404.1:p.Thr4del
XM_017024916.1:c.10_12del	XP_016880405.1:p.Thr4del
XM_017024917.1:c.10_12del	XP_016880406.1:p.Thr4del
XM_017024918.2:c.10_12del	XP_016880407.1:p.Thr4del
XM_017024919.1:c.10_12del	XP_016880408.1:p.Thr4del
XR_934513.3:n.865_867del
XR_934514.3:n.865_867del
NM_058216.3:c.361_363del MANE Select	NP_478123.1:p.Thr121del
NR_103872.2:n.403_405del
NM_002876.4:c.361_363del	NP_002867.1:p.Thr121del