Canonical Allele Identifier: CA501075273

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 751657
• ClinVar RCV Id: RCV001470694
• dbSNP Id: rs1598473581
• MyVariant Identifiers: chr17:g.56780678A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703317A>G , CM000679.2:g.58703317A>G	GRCh38
NC_000017.10:g.56780678A>G , CM000679.1:g.56780678A>G	GRCh37
NC_000017.9:g.54135677A>G	NCBI36
NG_023199.1:g.15716A>G , LRG_314:g.15716A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.342A>G	ENSP00000464056.2:p.Ser114=
ENST00000697677.1:n.1774A>G
ENST00000697678.1:n.595A>G
ENST00000697679.1:n.1767A>G
ENST00000697680.1:c.*1557A>G	ENSP00000513392.1:n.*1557A>G
ENST00000697681.1:c.*1709A>G	ENSP00000513393.1:n.*1709A>G
ENST00000697683.1:c.*1557A>G	ENSP00000513395.1:n.*1557A>G
ENST00000697684.1:n.753A>G
ENST00000697685.1:c.*1390A>G	ENSP00000513396.1:n.*1390A>G
ENST00000697686.1:c.342A>G	ENSP00000513397.1:p.Ser114=
ENST00000697687.1:n.572A>G
ENST00000697688.1:n.739A>G
ENST00000697689.1:c.*1229A>G	ENSP00000513398.1:n.*1229A>G
ENST00000697690.1:c.693A>G	ENSP00000513399.1:p.Ser231=
ENST00000697691.1:c.*665A>G	ENSP00000513400.1:n.*665A>G
ENST00000697692.1:c.*705A>G	ENSP00000513401.1:n.*705A>G
ENST00000697694.1:c.342A>G	ENSP00000513402.1:p.Ser114=
ENST00000697695.1:n.1300A>G
ENST00000337432.9:c.693A>G MANE Select	ENSP00000336701.4:p.Ser231=
ENST00000337432.8:c.693A>G	ENSP00000336701.4:p.Ser231=
ENST00000413590.5:c.331A>G
ENST00000425173.5:c.489A>G	ENSP00000407282.1:p.Ser163=
ENST00000461271.5:c.342A>G	ENSP00000464056.1:p.Ser114=
ENST00000475762.5:c.*1396A>G	ENSP00000432421.1:n.*1396A>G
ENST00000482007.5:c.*121A>G	ENSP00000433332.1:n.*121A>G
ENST00000487525.5:c.*121A>G	ENSP00000431637.1:n.*121A>G
ENST00000487921.5:n.605A>G
ENST00000583539.5:c.693A>G	ENSP00000463121.1:p.Ser231=
ENST00000584617.5:c.415A>G
NM_058216.2:c.693A>G	NP_478123.1:p.Ser231=
NR_103872.1:n.597A>G
XM_006722001.2:c.693A>G	XP_006722064.1:p.Ser231=
XM_006722002.2:c.693A>G	XP_006722065.1:p.Ser231=
XM_006722004.2:c.342A>G	XP_006722067.1:p.Ser114=
XM_006722005.2:c.342A>G	XP_006722068.1:p.Ser114=
XM_011525092.1:c.342A>G	XP_011523394.1:p.Ser114=
XM_011525093.1:c.342A>G	XP_011523395.1:p.Ser114=
XM_011525094.1:c.342A>G	XP_011523396.1:p.Ser114=
XR_934513.1:n.766A>G
XR_934514.1:n.766A>G
XM_006722001.4:c.693A>G	XP_006722064.1:p.Ser231=
XM_006722002.4:c.693A>G	XP_006722065.1:p.Ser231=
XM_006722004.3:c.342A>G	XP_006722067.1:p.Ser114=
XM_006722005.3:c.342A>G	XP_006722068.1:p.Ser114=
XM_011525092.2:c.342A>G	XP_011523394.1:p.Ser114=
XM_011525093.2:c.342A>G	XP_011523395.1:p.Ser114=
XM_011525094.2:c.342A>G	XP_011523396.1:p.Ser114=
XM_017024914.1:c.342A>G	XP_016880403.1:p.Ser114=
XM_017024915.1:c.342A>G	XP_016880404.1:p.Ser114=
XM_017024916.1:c.342A>G	XP_016880405.1:p.Ser114=
XM_017024917.1:c.342A>G	XP_016880406.1:p.Ser114=
XM_017024918.2:c.342A>G	XP_016880407.1:p.Ser114=
XM_017024919.1:c.342A>G	XP_016880408.1:p.Ser114=
XR_934513.3:n.1197A>G
XR_934514.3:n.1197A>G
NM_058216.3:c.693A>G MANE Select	NP_478123.1:p.Ser231=
NR_103872.2:n.568A>G