Canonical Allele Identifier: CA16615453

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 409847
• ClinVar RCV Id: RCV000471166 ; RCV001024846 ; RCV003470461
• dbSNP Id: rs1060502591
• MyVariant Identifiers: chr17:g.56780590A>G (hg19) ; chr17:g.58703229A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703229A>G , CM000679.2:g.58703229A>G	GRCh38
NC_000017.10:g.56780590A>G , CM000679.1:g.56780590A>G	GRCh37
NC_000017.9:g.54135589A>G	NCBI36
NG_023199.1:g.15628A>G , LRG_314:g.15628A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.254A>G	ENSP00000464056.2:p.Asp85Gly
ENST00000697677.1:n.1686A>G
ENST00000697678.1:n.507A>G
ENST00000697679.1:n.1679A>G
ENST00000697680.1:c.*1469A>G	ENSP00000513392.1:n.*1469A>G
ENST00000697681.1:c.*1621A>G	ENSP00000513393.1:n.*1621A>G
ENST00000697683.1:c.*1469A>G	ENSP00000513395.1:n.*1469A>G
ENST00000697684.1:n.665A>G
ENST00000697685.1:c.*1302A>G	ENSP00000513396.1:n.*1302A>G
ENST00000697686.1:c.254A>G	ENSP00000513397.1:p.Asp85Gly
ENST00000697687.1:n.484A>G
ENST00000697688.1:n.651A>G
ENST00000697689.1:c.*1141A>G	ENSP00000513398.1:n.*1141A>G
ENST00000697690.1:c.605A>G	ENSP00000513399.1:p.Asp202Gly
ENST00000697691.1:c.*577A>G	ENSP00000513400.1:n.*577A>G
ENST00000697692.1:c.*617A>G	ENSP00000513401.1:n.*617A>G
ENST00000697694.1:c.254A>G	ENSP00000513402.1:p.Asp85Gly
ENST00000697695.1:n.1212A>G
ENST00000337432.9:c.605A>G MANE Select	ENSP00000336701.4:p.Asp202Gly
ENST00000337432.8:c.605A>G	ENSP00000336701.4:p.Asp202Gly
ENST00000413590.5:c.243A>G
ENST00000425173.5:c.401A>G	ENSP00000407282.1:p.Asp134Gly
ENST00000461271.5:c.254A>G	ENSP00000464056.1:p.Asp85Gly
ENST00000475762.5:c.*1308A>G	ENSP00000432421.1:n.*1308A>G
ENST00000482007.5:c.*33A>G	ENSP00000433332.1:n.*33A>G
ENST00000487525.5:c.*33A>G	ENSP00000431637.1:n.*33A>G
ENST00000487921.5:n.517A>G
ENST00000583539.5:c.605A>G	ENSP00000463121.1:p.Asp202Gly
ENST00000584617.5:c.327A>G
NM_058216.2:c.605A>G	NP_478123.1:p.Asp202Gly
NR_103872.1:n.509A>G
XM_006722001.2:c.605A>G	XP_006722064.1:p.Asp202Gly
XM_006722002.2:c.605A>G	XP_006722065.1:p.Asp202Gly
XM_006722004.2:c.254A>G	XP_006722067.1:p.Asp85Gly
XM_006722005.2:c.254A>G	XP_006722068.1:p.Asp85Gly
XM_011525092.1:c.254A>G	XP_011523394.1:p.Asp85Gly
XM_011525093.1:c.254A>G	XP_011523395.1:p.Asp85Gly
XM_011525094.1:c.254A>G	XP_011523396.1:p.Asp85Gly
XR_934513.1:n.678A>G
XR_934514.1:n.678A>G
XM_006722001.4:c.605A>G	XP_006722064.1:p.Asp202Gly
XM_006722002.4:c.605A>G	XP_006722065.1:p.Asp202Gly
XM_006722004.3:c.254A>G	XP_006722067.1:p.Asp85Gly
XM_006722005.3:c.254A>G	XP_006722068.1:p.Asp85Gly
XM_011525092.2:c.254A>G	XP_011523394.1:p.Asp85Gly
XM_011525093.2:c.254A>G	XP_011523395.1:p.Asp85Gly
XM_011525094.2:c.254A>G	XP_011523396.1:p.Asp85Gly
XM_017024914.1:c.254A>G	XP_016880403.1:p.Asp85Gly
XM_017024915.1:c.254A>G	XP_016880404.1:p.Asp85Gly
XM_017024916.1:c.254A>G	XP_016880405.1:p.Asp85Gly
XM_017024917.1:c.254A>G	XP_016880406.1:p.Asp85Gly
XM_017024918.2:c.254A>G	XP_016880407.1:p.Asp85Gly
XM_017024919.1:c.254A>G	XP_016880408.1:p.Asp85Gly
XR_934513.3:n.1109A>G
XR_934514.3:n.1109A>G
NM_058216.3:c.605A>G MANE Select	NP_478123.1:p.Asp202Gly
NR_103872.2:n.480A>G