Canonical Allele Identifier: CA2580094404

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1737545
• ClinVar RCV Id: RCV002321464 ; RCV004051258

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696695_58696708del , CM000679.2:g.58696695_58696708del	GRCh38
NC_000017.10:g.56774056_56774069del , CM000679.1:g.56774056_56774069del	GRCh37
NC_000017.9:g.54129055_54129068del	NCBI36
NG_023199.1:g.9094_9107del , LRG_314:g.9094_9107del
NG_047169.1:g.377_390del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.56_69del
ENST00000697675.1:n.3004_3017del
ENST00000697676.1:n.467_480del
ENST00000697677.1:n.1488_1501del
ENST00000697678.1:n.309_322del
ENST00000697679.1:n.1481_1494del
ENST00000697680.1:c.*1271_*1284del
ENST00000697681.1:c.*1298_*1311del
ENST00000697683.1:c.*1271_*1284del
ENST00000697684.1:n.467_480del
ENST00000697685.1:c.*1268+1506_*1268+1519del	ENSP00000513396.1:n.*1268+1506_*1268+1519del
ENST00000697686.1:c.56_69del
ENST00000697687.1:n.450+1506_450+1519del
ENST00000697688.1:n.453_466del
ENST00000697689.1:c.*1107+1506_*1107+1519del	ENSP00000513398.1:n.*1107+1506_*1107+1519del
ENST00000697690.1:c.407_420del
ENST00000697691.1:c.*379_*392del
ENST00000697692.1:c.*419_*432del
ENST00000697694.1:c.56_69del
ENST00000697695.1:n.1014_1027del
ENST00000337432.9:c.407_420del
ENST00000337432.8:c.407_420del
ENST00000413590.5:c.45_58del
ENST00000425173.5:c.203_216del
ENST00000461271.5:c.56_69del
ENST00000475762.5:c.*1110_*1123del
ENST00000482007.5:c.404+1506_404+1519del	ENSP00000433332.1:n.404+1506_404+1519del
ENST00000487525.5:c.404+1506_404+1519del	ENSP00000431637.1:n.404+1506_404+1519del
ENST00000487921.5:n.319_332del
ENST00000583539.5:c.407_420del
ENST00000584617.5:c.129_142del
ENST00000622327.4:c.143_156del
NM_058216.2:c.407_420del
NR_103872.1:n.475+1506_475+1519del
XM_006722001.2:c.407_420del
XM_006722002.2:c.407_420del
XM_006722004.2:c.56_69del
XM_006722005.2:c.56_69del
XM_011525092.1:c.56_69del
XM_011525093.1:c.56_69del
XM_011525094.1:c.56_69del
XR_934513.1:n.480_493del
XR_934514.1:n.480_493del
XM_006722001.4:c.407_420del
XM_006722002.4:c.407_420del
XM_006722004.3:c.56_69del
XM_006722005.3:c.56_69del
XM_011525092.2:c.56_69del
XM_011525093.2:c.56_69del
XM_011525094.2:c.56_69del
XM_017024914.1:c.56_69del
XM_017024915.1:c.56_69del
XM_017024916.1:c.56_69del
XM_017024917.1:c.56_69del
XM_017024918.2:c.56_69del
XM_017024919.1:c.56_69del
XR_934513.3:n.911_924del
XR_934514.3:n.911_924del
NM_058216.3:c.407_420del
NR_103872.2:n.446+1506_446+1519del