Canonical Allele Identifier: CA400359301

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 480508
• ClinVar RCV Id: RCV000561624 ; RCV000648242 ; RCV002259351 ; RCV003470841
• dbSNP Id: rs748589398
• gnomAD v4: 17-58720744-A-G
• MyVariant Identifiers: chr17:g.56798105A>G (hg19) ; chr17:g.58720744A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58720744A>G , CM000679.2:g.58720744A>G	GRCh38
NC_000017.10:g.56798105A>G , CM000679.1:g.56798105A>G	GRCh37
NC_000017.9:g.54153104A>G	NCBI36
NG_023199.1:g.33143A>G , LRG_314:g.33143A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.487-2A>G	ENSP00000464056.2:n.487-2A>G
ENST00000697678.1:n.740-2A>G
ENST00000697679.1:n.1912-2A>G
ENST00000697680.1:c.*1802-2A>G	ENSP00000513392.1:n.*1802-2A>G
ENST00000697681.1:c.*1999-2A>G	ENSP00000513393.1:n.*1999-2A>G
ENST00000697683.1:c.*1702-2A>G	ENSP00000513395.1:n.*1702-2A>G
ENST00000697684.1:n.898-2A>G
ENST00000697685.1:c.*1535-2A>G	ENSP00000513396.1:n.*1535-2A>G
ENST00000697686.1:c.487-2A>G	ENSP00000513397.1:n.487-2A>G
ENST00000697687.1:n.717-2A>G
ENST00000697688.1:n.884-2A>G
ENST00000697689.1:c.*1374-2A>G	ENSP00000513398.1:n.*1374-2A>G
ENST00000697690.1:c.838-2A>G	ENSP00000513399.1:n.838-2A>G
ENST00000697691.1:c.*810-2A>G	ENSP00000513400.1:n.*810-2A>G
ENST00000697692.1:c.*850-2A>G	ENSP00000513401.1:n.*850-2A>G
ENST00000697694.1:c.487-2A>G	ENSP00000513402.1:n.487-2A>G
ENST00000697695.1:n.1445-2A>G
ENST00000337432.9:c.838-2A>G MANE Select	ENSP00000336701.4:n.838-2A>G
ENST00000337432.8:c.838-2A>G	ENSP00000336701.4:n.838-2A>G
ENST00000413590.5:c.476-2A>G
ENST00000475762.5:c.*1541-3296A>G	ENSP00000432421.1:n.*1541-3296A>G
ENST00000482007.5:c.*266-2A>G	ENSP00000433332.1:n.*266-2A>G
ENST00000487525.5:c.*411-2A>G	ENSP00000431637.1:n.*411-2A>G
ENST00000578151.1:n.173-2A>G
ENST00000581221.5:n.353-2A>G
ENST00000583539.5:c.838-2A>G	ENSP00000463121.1:n.838-2A>G
ENST00000584617.5:c.560-2A>G
ENST00000584804.1:c.133-2A>G	ENSP00000463658.1:n.133-2A>G
NM_058216.2:c.838-2A>G	NP_478123.1:n.838-2A>G
NR_103872.1:n.742-2A>G
XM_006722001.2:c.838-2A>G	XP_006722064.1:n.838-2A>G
XM_006722002.2:c.838-2A>G	XP_006722065.1:n.838-2A>G
XM_006722004.2:c.487-2A>G	XP_006722067.1:n.487-2A>G
XM_006722005.2:c.487-2A>G	XP_006722068.1:n.487-2A>G
XM_011525092.1:c.487-2A>G	XP_011523394.1:n.487-2A>G
XM_011525093.1:c.487-2A>G	XP_011523395.1:n.487-2A>G
XM_011525094.1:c.487-2A>G	XP_011523396.1:n.487-2A>G
XR_934513.1:n.1056-2A>G
XR_934514.1:n.1056-2A>G
XM_006722001.4:c.838-2A>G	XP_006722064.1:n.838-2A>G
XM_006722002.4:c.838-2A>G	XP_006722065.1:n.838-2A>G
XM_006722004.3:c.487-2A>G	XP_006722067.1:n.487-2A>G
XM_006722005.3:c.487-2A>G	XP_006722068.1:n.487-2A>G
XM_011525092.2:c.487-2A>G	XP_011523394.1:n.487-2A>G
XM_011525093.2:c.487-2A>G	XP_011523395.1:n.487-2A>G
XM_011525094.2:c.487-2A>G	XP_011523396.1:n.487-2A>G
XM_017024914.1:c.487-2A>G	XP_016880403.1:n.487-2A>G
XM_017024915.1:c.487-2A>G	XP_016880404.1:n.487-2A>G
XM_017024916.1:c.487-2A>G	XP_016880405.1:n.487-2A>G
XM_017024917.1:c.487-2A>G	XP_016880406.1:n.487-2A>G
XM_017024918.2:c.487-2A>G	XP_016880407.1:n.487-2A>G
XM_017024919.1:c.487-2A>G	XP_016880408.1:n.487-2A>G
XR_934513.3:n.1487-2A>G
XR_934514.3:n.1487-2A>G
NM_058216.3:c.838-2A>G MANE Select	NP_478123.1:n.838-2A>G
NR_103872.2:n.713-2A>G