Canonical Allele Identifier: CA400350133

Gene: RAD51C

Linked Data

• dbSNP Id: rs2143802226
• MyVariant Identifiers: chr17:g.56780684C>G (hg19) ; chr17:g.58703323C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703323C>G , CM000679.2:g.58703323C>G	GRCh38
NC_000017.10:g.56780684C>G , CM000679.1:g.56780684C>G	GRCh37
NC_000017.9:g.54135683C>G	NCBI36
NG_023199.1:g.15722C>G , LRG_314:g.15722C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.348C>G	ENSP00000464056.2:p.His116Gln
ENST00000697677.1:n.1780C>G
ENST00000697678.1:n.601C>G
ENST00000697679.1:n.1773C>G
ENST00000697680.1:c.*1563C>G	ENSP00000513392.1:n.*1563C>G
ENST00000697681.1:c.*1715C>G	ENSP00000513393.1:n.*1715C>G
ENST00000697683.1:c.*1563C>G	ENSP00000513395.1:n.*1563C>G
ENST00000697684.1:n.759C>G
ENST00000697685.1:c.*1396C>G	ENSP00000513396.1:n.*1396C>G
ENST00000697686.1:c.348C>G	ENSP00000513397.1:p.His116Gln
ENST00000697687.1:n.578C>G
ENST00000697688.1:n.745C>G
ENST00000697689.1:c.*1235C>G	ENSP00000513398.1:n.*1235C>G
ENST00000697690.1:c.699C>G	ENSP00000513399.1:p.His233Gln
ENST00000697691.1:c.*671C>G	ENSP00000513400.1:n.*671C>G
ENST00000697692.1:c.*711C>G	ENSP00000513401.1:n.*711C>G
ENST00000697694.1:c.348C>G	ENSP00000513402.1:p.His116Gln
ENST00000697695.1:n.1306C>G
ENST00000337432.9:c.699C>G MANE Select	ENSP00000336701.4:p.His233Gln
ENST00000337432.8:c.699C>G	ENSP00000336701.4:p.His233Gln
ENST00000413590.5:c.337C>G
ENST00000425173.5:c.495C>G	ENSP00000407282.1:p.His165Gln
ENST00000461271.5:c.348C>G	ENSP00000464056.1:p.His116Gln
ENST00000475762.5:c.*1402C>G	ENSP00000432421.1:n.*1402C>G
ENST00000482007.5:c.*127C>G	ENSP00000433332.1:n.*127C>G
ENST00000487525.5:c.*127C>G	ENSP00000431637.1:n.*127C>G
ENST00000487921.5:n.611C>G
ENST00000583539.5:c.699C>G	ENSP00000463121.1:p.His233Gln
ENST00000584617.5:c.421C>G
NM_058216.2:c.699C>G	NP_478123.1:p.His233Gln
NR_103872.1:n.603C>G
XM_006722001.2:c.699C>G	XP_006722064.1:p.His233Gln
XM_006722002.2:c.699C>G	XP_006722065.1:p.His233Gln
XM_006722004.2:c.348C>G	XP_006722067.1:p.His116Gln
XM_006722005.2:c.348C>G	XP_006722068.1:p.His116Gln
XM_011525092.1:c.348C>G	XP_011523394.1:p.His116Gln
XM_011525093.1:c.348C>G	XP_011523395.1:p.His116Gln
XM_011525094.1:c.348C>G	XP_011523396.1:p.His116Gln
XR_934513.1:n.772C>G
XR_934514.1:n.772C>G
XM_006722001.4:c.699C>G	XP_006722064.1:p.His233Gln
XM_006722002.4:c.699C>G	XP_006722065.1:p.His233Gln
XM_006722004.3:c.348C>G	XP_006722067.1:p.His116Gln
XM_006722005.3:c.348C>G	XP_006722068.1:p.His116Gln
XM_011525092.2:c.348C>G	XP_011523394.1:p.His116Gln
XM_011525093.2:c.348C>G	XP_011523395.1:p.His116Gln
XM_011525094.2:c.348C>G	XP_011523396.1:p.His116Gln
XM_017024914.1:c.348C>G	XP_016880403.1:p.His116Gln
XM_017024915.1:c.348C>G	XP_016880404.1:p.His116Gln
XM_017024916.1:c.348C>G	XP_016880405.1:p.His116Gln
XM_017024917.1:c.348C>G	XP_016880406.1:p.His116Gln
XM_017024918.2:c.348C>G	XP_016880407.1:p.His116Gln
XM_017024919.1:c.348C>G	XP_016880408.1:p.His116Gln
XR_934513.3:n.1203C>G
XR_934514.3:n.1203C>G
NM_058216.3:c.699C>G MANE Select	NP_478123.1:p.His233Gln
NR_103872.2:n.574C>G