Canonical Allele Identifier: CA400350122

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1058320
• ClinVar RCV Id: RCV001367444
• dbSNP Id: rs2143802148
• MyVariant Identifiers: chr17:g.56780682C>T (hg19) ; chr17:g.58703321C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703321C>T , CM000679.2:g.58703321C>T	GRCh38
NC_000017.10:g.56780682C>T , CM000679.1:g.56780682C>T	GRCh37
NC_000017.9:g.54135681C>T	NCBI36
NG_023199.1:g.15720C>T , LRG_314:g.15720C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.346C>T	ENSP00000464056.2:p.His116Tyr
ENST00000697677.1:n.1778C>T
ENST00000697678.1:n.599C>T
ENST00000697679.1:n.1771C>T
ENST00000697680.1:c.*1561C>T	ENSP00000513392.1:n.*1561C>T
ENST00000697681.1:c.*1713C>T	ENSP00000513393.1:n.*1713C>T
ENST00000697683.1:c.*1561C>T	ENSP00000513395.1:n.*1561C>T
ENST00000697684.1:n.757C>T
ENST00000697685.1:c.*1394C>T	ENSP00000513396.1:n.*1394C>T
ENST00000697686.1:c.346C>T	ENSP00000513397.1:p.His116Tyr
ENST00000697687.1:n.576C>T
ENST00000697688.1:n.743C>T
ENST00000697689.1:c.*1233C>T	ENSP00000513398.1:n.*1233C>T
ENST00000697690.1:c.697C>T	ENSP00000513399.1:p.His233Tyr
ENST00000697691.1:c.*669C>T	ENSP00000513400.1:n.*669C>T
ENST00000697692.1:c.*709C>T	ENSP00000513401.1:n.*709C>T
ENST00000697694.1:c.346C>T	ENSP00000513402.1:p.His116Tyr
ENST00000697695.1:n.1304C>T
ENST00000337432.9:c.697C>T MANE Select	ENSP00000336701.4:p.His233Tyr
ENST00000337432.8:c.697C>T	ENSP00000336701.4:p.His233Tyr
ENST00000413590.5:c.335C>T
ENST00000425173.5:c.493C>T	ENSP00000407282.1:p.His165Tyr
ENST00000461271.5:c.346C>T	ENSP00000464056.1:p.His116Tyr
ENST00000475762.5:c.*1400C>T	ENSP00000432421.1:n.*1400C>T
ENST00000482007.5:c.*125C>T	ENSP00000433332.1:n.*125C>T
ENST00000487525.5:c.*125C>T	ENSP00000431637.1:n.*125C>T
ENST00000487921.5:n.609C>T
ENST00000583539.5:c.697C>T	ENSP00000463121.1:p.His233Tyr
ENST00000584617.5:c.419C>T
NM_058216.2:c.697C>T	NP_478123.1:p.His233Tyr
NR_103872.1:n.601C>T
XM_006722001.2:c.697C>T	XP_006722064.1:p.His233Tyr
XM_006722002.2:c.697C>T	XP_006722065.1:p.His233Tyr
XM_006722004.2:c.346C>T	XP_006722067.1:p.His116Tyr
XM_006722005.2:c.346C>T	XP_006722068.1:p.His116Tyr
XM_011525092.1:c.346C>T	XP_011523394.1:p.His116Tyr
XM_011525093.1:c.346C>T	XP_011523395.1:p.His116Tyr
XM_011525094.1:c.346C>T	XP_011523396.1:p.His116Tyr
XR_934513.1:n.770C>T
XR_934514.1:n.770C>T
XM_006722001.4:c.697C>T	XP_006722064.1:p.His233Tyr
XM_006722002.4:c.697C>T	XP_006722065.1:p.His233Tyr
XM_006722004.3:c.346C>T	XP_006722067.1:p.His116Tyr
XM_006722005.3:c.346C>T	XP_006722068.1:p.His116Tyr
XM_011525092.2:c.346C>T	XP_011523394.1:p.His116Tyr
XM_011525093.2:c.346C>T	XP_011523395.1:p.His116Tyr
XM_011525094.2:c.346C>T	XP_011523396.1:p.His116Tyr
XM_017024914.1:c.346C>T	XP_016880403.1:p.His116Tyr
XM_017024915.1:c.346C>T	XP_016880404.1:p.His116Tyr
XM_017024916.1:c.346C>T	XP_016880405.1:p.His116Tyr
XM_017024917.1:c.346C>T	XP_016880406.1:p.His116Tyr
XM_017024918.2:c.346C>T	XP_016880407.1:p.His116Tyr
XM_017024919.1:c.346C>T	XP_016880408.1:p.His116Tyr
XR_934513.3:n.1201C>T
XR_934514.3:n.1201C>T
NM_058216.3:c.697C>T MANE Select	NP_478123.1:p.His233Tyr
NR_103872.2:n.572C>T