Canonical Allele Identifier: CA400361341

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 918247
• ClinVar RCV Id: RCV001175743 ; RCV003462645 ; RCV003769864
• dbSNP Id: rs2049021589
• MyVariant Identifiers: chr17:g.56801416A>G (hg19) ; chr17:g.58724055A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724055A>G , CM000679.2:g.58724055A>G	GRCh38
NC_000017.10:g.56801416A>G , CM000679.1:g.56801416A>G	GRCh37
NC_000017.9:g.54156415A>G	NCBI36
NG_023199.1:g.36454A>G , LRG_314:g.36454A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.569A>G	ENSP00000464056.2:p.His190Arg
ENST00000697680.1:c.*1884A>G	ENSP00000513392.1:n.*1884A>G
ENST00000697681.1:c.*2081A>G	ENSP00000513393.1:n.*2081A>G
ENST00000697683.1:c.*1784A>G	ENSP00000513395.1:n.*1784A>G
ENST00000697684.1:n.980A>G
ENST00000697685.1:c.*1617A>G	ENSP00000513396.1:n.*1617A>G
ENST00000697686.1:c.569A>G	ENSP00000513397.1:p.His190Arg
ENST00000697687.1:n.799A>G
ENST00000697688.1:n.966A>G
ENST00000697689.1:c.*1440+3243A>G	ENSP00000513398.1:n.*1440+3243A>G
ENST00000697690.1:c.904+3243A>G	ENSP00000513399.1:n.904+3243A>G
ENST00000697691.1:c.*892A>G	ENSP00000513400.1:n.*892A>G
ENST00000697692.1:c.*932A>G	ENSP00000513401.1:n.*932A>G
ENST00000697694.1:c.569A>G	ENSP00000513402.1:p.His190Arg
ENST00000697695.1:n.1527A>G
ENST00000337432.9:c.920A>G MANE Select	ENSP00000336701.4:p.His307Arg
ENST00000337432.8:c.920A>G	ENSP00000336701.4:p.His307Arg
ENST00000413590.5:c.558A>G
ENST00000475762.5:c.*1556A>G	ENSP00000432421.1:n.*1556A>G
ENST00000482007.5:c.*348A>G	ENSP00000433332.1:n.*348A>G
ENST00000487525.5:c.*493A>G	ENSP00000431637.1:n.*493A>G
ENST00000578151.1:n.239+3243A>G
ENST00000581221.5:n.435A>G
ENST00000583539.5:c.920A>G	ENSP00000463121.1:p.His307Arg
ENST00000584617.5:c.642A>G
ENST00000584804.1:c.199+3243A>G	ENSP00000463658.1:n.199+3243A>G
NM_058216.2:c.920A>G	NP_478123.1:p.His307Arg
NR_103872.1:n.824A>G
XM_006722001.2:c.920A>G	XP_006722064.1:p.His307Arg
XM_006722002.2:c.904+3243A>G	XP_006722065.1:n.904+3243A>G
XM_006722004.2:c.569A>G	XP_006722067.1:p.His190Arg
XM_006722005.2:c.569A>G	XP_006722068.1:p.His190Arg
XM_011525092.1:c.569A>G	XP_011523394.1:p.His190Arg
XM_011525093.1:c.569A>G	XP_011523395.1:p.His190Arg
XM_011525094.1:c.569A>G	XP_011523396.1:p.His190Arg
XR_934513.1:n.1138A>G
XR_934514.1:n.1138A>G
XM_006722001.4:c.920A>G	XP_006722064.1:p.His307Arg
XM_006722002.4:c.904+3243A>G	XP_006722065.1:n.904+3243A>G
XM_006722004.3:c.569A>G	XP_006722067.1:p.His190Arg
XM_006722005.3:c.569A>G	XP_006722068.1:p.His190Arg
XM_011525092.2:c.569A>G	XP_011523394.1:p.His190Arg
XM_011525093.2:c.569A>G	XP_011523395.1:p.His190Arg
XM_011525094.2:c.569A>G	XP_011523396.1:p.His190Arg
XM_017024914.1:c.569A>G	XP_016880403.1:p.His190Arg
XM_017024915.1:c.569A>G	XP_016880404.1:p.His190Arg
XM_017024916.1:c.569A>G	XP_016880405.1:p.His190Arg
XM_017024917.1:c.569A>G	XP_016880406.1:p.His190Arg
XM_017024918.2:c.569A>G	XP_016880407.1:p.His190Arg
XM_017024919.1:c.553+3243A>G	XP_016880408.1:n.553+3243A>G
XR_934513.3:n.1569A>G
XR_934514.3:n.1569A>G
NM_058216.3:c.920A>G MANE Select	NP_478123.1:p.His307Arg
NR_103872.2:n.795A>G