Canonical Allele Identifier: CA2573154400

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1439892
• ClinVar RCV Id: RCV001965418
• dbSNP Id: rs2143801795

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703316del , CM000679.2:g.58703316del	GRCh38
NC_000017.10:g.56780677del , CM000679.1:g.56780677del	GRCh37
NC_000017.9:g.54135676del	NCBI36
NG_023199.1:g.15715del , LRG_314:g.15715del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.341del	ENSP00000464056.2:p.Ser114Ter
ENST00000697677.1:n.1773del
ENST00000697678.1:n.594del
ENST00000697679.1:n.1766del
ENST00000697680.1:c.*1556del	ENSP00000513392.1:n.*1556del
ENST00000697681.1:c.*1708del	ENSP00000513393.1:n.*1708del
ENST00000697683.1:c.*1556del	ENSP00000513395.1:n.*1556del
ENST00000697684.1:n.752del
ENST00000697685.1:c.*1389del	ENSP00000513396.1:n.*1389del
ENST00000697686.1:c.341del	ENSP00000513397.1:p.Ser114Ter
ENST00000697687.1:n.571del
ENST00000697688.1:n.738del
ENST00000697689.1:c.*1228del	ENSP00000513398.1:n.*1228del
ENST00000697690.1:c.692del	ENSP00000513399.1:p.Ser231Ter
ENST00000697691.1:c.*664del	ENSP00000513400.1:n.*664del
ENST00000697692.1:c.*704del	ENSP00000513401.1:n.*704del
ENST00000697694.1:c.341del	ENSP00000513402.1:p.Ser114Ter
ENST00000697695.1:n.1299del
ENST00000337432.9:c.692del MANE Select	ENSP00000336701.4:p.Ser231Ter
ENST00000337432.8:c.692del	ENSP00000336701.4:p.Ser231Ter
ENST00000413590.5:c.330del
ENST00000425173.5:c.488del	ENSP00000407282.1:p.Ser163Ter
ENST00000461271.5:c.341del	ENSP00000464056.1:p.Ser114Ter
ENST00000475762.5:c.*1395del	ENSP00000432421.1:n.*1395del
ENST00000482007.5:c.*120del	ENSP00000433332.1:n.*120del
ENST00000487525.5:c.*120del	ENSP00000431637.1:n.*120del
ENST00000487921.5:n.604del
ENST00000583539.5:c.692del	ENSP00000463121.1:p.Ser231Ter
ENST00000584617.5:c.414del
NM_058216.2:c.692del	NP_478123.1:p.Ser231Ter
NR_103872.1:n.596del
XM_006722001.2:c.692del	XP_006722064.1:p.Ser231Ter
XM_006722002.2:c.692del	XP_006722065.1:p.Ser231Ter
XM_006722004.2:c.341del	XP_006722067.1:p.Ser114Ter
XM_006722005.2:c.341del	XP_006722068.1:p.Ser114Ter
XM_011525092.1:c.341del	XP_011523394.1:p.Ser114Ter
XM_011525093.1:c.341del	XP_011523395.1:p.Ser114Ter
XM_011525094.1:c.341del	XP_011523396.1:p.Ser114Ter
XR_934513.1:n.765del
XR_934514.1:n.765del
XM_006722001.4:c.692del	XP_006722064.1:p.Ser231Ter
XM_006722002.4:c.692del	XP_006722065.1:p.Ser231Ter
XM_006722004.3:c.341del	XP_006722067.1:p.Ser114Ter
XM_006722005.3:c.341del	XP_006722068.1:p.Ser114Ter
XM_011525092.2:c.341del	XP_011523394.1:p.Ser114Ter
XM_011525093.2:c.341del	XP_011523395.1:p.Ser114Ter
XM_011525094.2:c.341del	XP_011523396.1:p.Ser114Ter
XM_017024914.1:c.341del	XP_016880403.1:p.Ser114Ter
XM_017024915.1:c.341del	XP_016880404.1:p.Ser114Ter
XM_017024916.1:c.341del	XP_016880405.1:p.Ser114Ter
XM_017024917.1:c.341del	XP_016880406.1:p.Ser114Ter
XM_017024918.2:c.341del	XP_016880407.1:p.Ser114Ter
XM_017024919.1:c.341del	XP_016880408.1:p.Ser114Ter
XR_934513.3:n.1196del
XR_934514.3:n.1196del
NM_058216.3:c.692del MANE Select	NP_478123.1:p.Ser231Ter
NR_103872.2:n.567del