Canonical Allele Identifier: CA2267819524

Gene: RAD51C

Linked Data

• dbSNP Id: rs2048276781

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703334G>C , CM000679.2:g.58703334G>C	GRCh38
NC_000017.10:g.56780695G>C , CM000679.1:g.56780695G>C	GRCh37
NC_000017.9:g.54135694G>C	NCBI36
NG_023199.1:g.15733G>C , LRG_314:g.15733G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.354+5G>C	ENSP00000464056.2:n.354+5G>C
ENST00000697677.1:n.1791G>C
ENST00000697678.1:n.607+5G>C
ENST00000697679.1:n.1779+5G>C
ENST00000697680.1:c.*1569+5G>C	ENSP00000513392.1:n.*1569+5G>C
ENST00000697681.1:c.*1721+5G>C	ENSP00000513393.1:n.*1721+5G>C
ENST00000697683.1:c.*1569+5G>C	ENSP00000513395.1:n.*1569+5G>C
ENST00000697684.1:n.765+5G>C
ENST00000697685.1:c.*1402+5G>C	ENSP00000513396.1:n.*1402+5G>C
ENST00000697686.1:c.354+5G>C	ENSP00000513397.1:n.354+5G>C
ENST00000697687.1:n.584+5G>C
ENST00000697688.1:n.751+5G>C
ENST00000697689.1:c.*1241+5G>C	ENSP00000513398.1:n.*1241+5G>C
ENST00000697690.1:c.705+5G>C	ENSP00000513399.1:n.705+5G>C
ENST00000697691.1:c.*677+5G>C	ENSP00000513400.1:n.*677+5G>C
ENST00000697692.1:c.*717+5G>C	ENSP00000513401.1:n.*717+5G>C
ENST00000697694.1:c.354+5G>C	ENSP00000513402.1:n.354+5G>C
ENST00000697695.1:n.1312+5G>C
ENST00000337432.9:c.705+5G>C MANE Select	ENSP00000336701.4:n.705+5G>C
ENST00000337432.8:c.705+5G>C	ENSP00000336701.4:n.705+5G>C
ENST00000413590.5:c.343+5G>C
ENST00000425173.5:c.501+5G>C	ENSP00000407282.1:n.501+5G>C
ENST00000461271.5:c.354+5G>C	ENSP00000464056.1:n.354+5G>C
ENST00000475762.5:c.*1408+5G>C	ENSP00000432421.1:n.*1408+5G>C
ENST00000482007.5:c.*133+5G>C	ENSP00000433332.1:n.*133+5G>C
ENST00000487525.5:c.*133+5G>C	ENSP00000431637.1:n.*133+5G>C
ENST00000487921.5:n.617+5G>C
ENST00000583539.5:c.705+5G>C	ENSP00000463121.1:n.705+5G>C
ENST00000584617.5:c.427+5G>C
NM_058216.2:c.705+5G>C	NP_478123.1:n.705+5G>C
NR_103872.1:n.609+5G>C
XM_006722001.2:c.705+5G>C	XP_006722064.1:n.705+5G>C
XM_006722002.2:c.705+5G>C	XP_006722065.1:n.705+5G>C
XM_006722004.2:c.354+5G>C	XP_006722067.1:n.354+5G>C
XM_006722005.2:c.354+5G>C	XP_006722068.1:n.354+5G>C
XM_011525092.1:c.354+5G>C	XP_011523394.1:n.354+5G>C
XM_011525093.1:c.354+5G>C	XP_011523395.1:n.354+5G>C
XM_011525094.1:c.354+5G>C	XP_011523396.1:n.354+5G>C
XR_934513.1:n.778+5G>C
XR_934514.1:n.778+5G>C
XM_006722001.4:c.705+5G>C	XP_006722064.1:n.705+5G>C
XM_006722002.4:c.705+5G>C	XP_006722065.1:n.705+5G>C
XM_006722004.3:c.354+5G>C	XP_006722067.1:n.354+5G>C
XM_006722005.3:c.354+5G>C	XP_006722068.1:n.354+5G>C
XM_011525092.2:c.354+5G>C	XP_011523394.1:n.354+5G>C
XM_011525093.2:c.354+5G>C	XP_011523395.1:n.354+5G>C
XM_011525094.2:c.354+5G>C	XP_011523396.1:n.354+5G>C
XM_017024914.1:c.354+5G>C	XP_016880403.1:n.354+5G>C
XM_017024915.1:c.354+5G>C	XP_016880404.1:n.354+5G>C
XM_017024916.1:c.354+5G>C	XP_016880405.1:n.354+5G>C
XM_017024917.1:c.354+5G>C	XP_016880406.1:n.354+5G>C
XM_017024918.2:c.354+5G>C	XP_016880407.1:n.354+5G>C
XM_017024919.1:c.354+5G>C	XP_016880408.1:n.354+5G>C
XR_934513.3:n.1209+5G>C
XR_934514.3:n.1209+5G>C
NM_058216.3:c.705+5G>C MANE Select	NP_478123.1:n.705+5G>C
NR_103872.2:n.580+5G>C