Canonical Allele Identifier: CA16615742

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 409867
• ClinVar RCV Id: RCV000468351 ; RCV000566618
• dbSNP Id: rs778157321
• MyVariant Identifiers: chr17:g.56780694T>G (hg19) ; chr17:g.58703333T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703333T>G , CM000679.2:g.58703333T>G	GRCh38
NC_000017.10:g.56780694T>G , CM000679.1:g.56780694T>G	GRCh37
NC_000017.9:g.54135693T>G	NCBI36
NG_023199.1:g.15732T>G , LRG_314:g.15732T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.354+4T>G	ENSP00000464056.2:n.354+4T>G
ENST00000697677.1:n.1790T>G
ENST00000697678.1:n.607+4T>G
ENST00000697679.1:n.1779+4T>G
ENST00000697680.1:c.*1569+4T>G	ENSP00000513392.1:n.*1569+4T>G
ENST00000697681.1:c.*1721+4T>G	ENSP00000513393.1:n.*1721+4T>G
ENST00000697683.1:c.*1569+4T>G	ENSP00000513395.1:n.*1569+4T>G
ENST00000697684.1:n.765+4T>G
ENST00000697685.1:c.*1402+4T>G	ENSP00000513396.1:n.*1402+4T>G
ENST00000697686.1:c.354+4T>G	ENSP00000513397.1:n.354+4T>G
ENST00000697687.1:n.584+4T>G
ENST00000697688.1:n.751+4T>G
ENST00000697689.1:c.*1241+4T>G	ENSP00000513398.1:n.*1241+4T>G
ENST00000697690.1:c.705+4T>G	ENSP00000513399.1:n.705+4T>G
ENST00000697691.1:c.*677+4T>G	ENSP00000513400.1:n.*677+4T>G
ENST00000697692.1:c.*717+4T>G	ENSP00000513401.1:n.*717+4T>G
ENST00000697694.1:c.354+4T>G	ENSP00000513402.1:n.354+4T>G
ENST00000697695.1:n.1312+4T>G
ENST00000337432.9:c.705+4T>G MANE Select	ENSP00000336701.4:n.705+4T>G
ENST00000337432.8:c.705+4T>G	ENSP00000336701.4:n.705+4T>G
ENST00000413590.5:c.343+4T>G
ENST00000425173.5:c.501+4T>G	ENSP00000407282.1:n.501+4T>G
ENST00000461271.5:c.354+4T>G	ENSP00000464056.1:n.354+4T>G
ENST00000475762.5:c.*1408+4T>G	ENSP00000432421.1:n.*1408+4T>G
ENST00000482007.5:c.*133+4T>G	ENSP00000433332.1:n.*133+4T>G
ENST00000487525.5:c.*133+4T>G	ENSP00000431637.1:n.*133+4T>G
ENST00000487921.5:n.617+4T>G
ENST00000583539.5:c.705+4T>G	ENSP00000463121.1:n.705+4T>G
ENST00000584617.5:c.427+4T>G
NM_058216.2:c.705+4T>G	NP_478123.1:n.705+4T>G
NR_103872.1:n.609+4T>G
XM_006722001.2:c.705+4T>G	XP_006722064.1:n.705+4T>G
XM_006722002.2:c.705+4T>G	XP_006722065.1:n.705+4T>G
XM_006722004.2:c.354+4T>G	XP_006722067.1:n.354+4T>G
XM_006722005.2:c.354+4T>G	XP_006722068.1:n.354+4T>G
XM_011525092.1:c.354+4T>G	XP_011523394.1:n.354+4T>G
XM_011525093.1:c.354+4T>G	XP_011523395.1:n.354+4T>G
XM_011525094.1:c.354+4T>G	XP_011523396.1:n.354+4T>G
XR_934513.1:n.778+4T>G
XR_934514.1:n.778+4T>G
XM_006722001.4:c.705+4T>G	XP_006722064.1:n.705+4T>G
XM_006722002.4:c.705+4T>G	XP_006722065.1:n.705+4T>G
XM_006722004.3:c.354+4T>G	XP_006722067.1:n.354+4T>G
XM_006722005.3:c.354+4T>G	XP_006722068.1:n.354+4T>G
XM_011525092.2:c.354+4T>G	XP_011523394.1:n.354+4T>G
XM_011525093.2:c.354+4T>G	XP_011523395.1:n.354+4T>G
XM_011525094.2:c.354+4T>G	XP_011523396.1:n.354+4T>G
XM_017024914.1:c.354+4T>G	XP_016880403.1:n.354+4T>G
XM_017024915.1:c.354+4T>G	XP_016880404.1:n.354+4T>G
XM_017024916.1:c.354+4T>G	XP_016880405.1:n.354+4T>G
XM_017024917.1:c.354+4T>G	XP_016880406.1:n.354+4T>G
XM_017024918.2:c.354+4T>G	XP_016880407.1:n.354+4T>G
XM_017024919.1:c.354+4T>G	XP_016880408.1:n.354+4T>G
XR_934513.3:n.1209+4T>G
XR_934514.3:n.1209+4T>G
NM_058216.3:c.705+4T>G MANE Select	NP_478123.1:n.705+4T>G
NR_103872.2:n.580+4T>G