Canonical Allele Identifier: CA299882

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 182834
• ClinVar RCV Id: RCV000160922 ; RCV000206110 ; RCV000218584 ; RCV001798558 ; RCV003467268
• dbSNP Id: rs730881930
• gnomAD v4: 17-58695180-C-G
• MyVariant Identifiers: chr17:g.56772541C>G (hg19) ; chr17:g.58695180C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695180C>G , CM000679.2:g.58695180C>G	GRCh38
NC_000017.10:g.56772541C>G , CM000679.1:g.56772541C>G	GRCh37
NC_000017.9:g.54127540C>G	NCBI36
NG_023199.1:g.7579C>G , LRG_314:g.7579C>G
NG_047169.1:g.1900G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.44C>G	ENSP00000464056.2:p.Thr15Arg
ENST00000697675.1:n.1489C>G
ENST00000697676.1:n.455C>G
ENST00000697677.1:n.1476C>G
ENST00000697678.1:n.297C>G
ENST00000697679.1:n.1469C>G
ENST00000697680.1:c.*1259C>G	ENSP00000513392.1:n.*1259C>G
ENST00000697681.1:c.*1259C>G	ENSP00000513393.1:n.*1259C>G
ENST00000697683.1:c.*1259C>G	ENSP00000513395.1:n.*1259C>G
ENST00000697684.1:n.455C>G
ENST00000697685.1:c.*1259C>G	ENSP00000513396.1:n.*1259C>G
ENST00000697686.1:c.44C>G	ENSP00000513397.1:p.Thr15Arg
ENST00000697687.1:n.441C>G
ENST00000697688.1:n.441C>G
ENST00000697689.1:c.*1098C>G	ENSP00000513398.1:n.*1098C>G
ENST00000697690.1:c.395C>G	ENSP00000513399.1:p.Thr132Arg
ENST00000697691.1:c.*367C>G	ENSP00000513400.1:n.*367C>G
ENST00000697692.1:c.*407C>G	ENSP00000513401.1:n.*407C>G
ENST00000697693.1:n.1170C>G
ENST00000697694.1:c.44C>G	ENSP00000513402.1:p.Thr15Arg
ENST00000697695.1:n.1002C>G
ENST00000337432.9:c.395C>G MANE Select	ENSP00000336701.4:p.Thr132Arg
ENST00000337432.8:c.395C>G	ENSP00000336701.4:p.Thr132Arg
ENST00000413590.5:c.33C>G
ENST00000421782.3:c.395C>G	ENSP00000391450.2:p.Thr132Arg
ENST00000425173.5:c.191C>G	ENSP00000407282.1:p.Thr64Arg
ENST00000461271.5:c.44C>G	ENSP00000464056.1:p.Thr15Arg
ENST00000475762.5:c.*1098C>G	ENSP00000432421.1:n.*1098C>G
ENST00000482007.5:c.395C>G	ENSP00000433332.1:p.Thr132Arg
ENST00000486827.1:c.*1259C>G	ENSP00000436761.1:n.*1259C>G
ENST00000487525.5:c.395C>G	ENSP00000431637.1:p.Thr132Arg
ENST00000487921.5:n.307C>G
ENST00000583539.5:c.395C>G	ENSP00000463121.1:p.Thr132Arg
ENST00000584617.5:c.127-1513C>G
ENST00000622327.4:c.131C>G	ENSP00000482326.1:p.Thr44Arg
NM_002876.3:c.395C>G	NP_002867.1:p.Thr132Arg
NM_058216.2:c.395C>G	NP_478123.1:p.Thr132Arg
NR_103872.1:n.466C>G
NR_103873.1:n.363C>G
XM_006722001.2:c.395C>G	XP_006722064.1:p.Thr132Arg
XM_006722002.2:c.395C>G	XP_006722065.1:p.Thr132Arg
XM_006722004.2:c.44C>G	XP_006722067.1:p.Thr15Arg
XM_006722005.2:c.44C>G	XP_006722068.1:p.Thr15Arg
XM_011525092.1:c.44C>G	XP_011523394.1:p.Thr15Arg
XM_011525093.1:c.44C>G	XP_011523395.1:p.Thr15Arg
XM_011525094.1:c.44C>G	XP_011523396.1:p.Thr15Arg
XR_934513.1:n.468C>G
XR_934514.1:n.468C>G
XM_006722001.4:c.395C>G	XP_006722064.1:p.Thr132Arg
XM_006722002.4:c.395C>G	XP_006722065.1:p.Thr132Arg
XM_006722004.3:c.44C>G	XP_006722067.1:p.Thr15Arg
XM_006722005.3:c.44C>G	XP_006722068.1:p.Thr15Arg
XM_011525092.2:c.44C>G	XP_011523394.1:p.Thr15Arg
XM_011525093.2:c.44C>G	XP_011523395.1:p.Thr15Arg
XM_011525094.2:c.44C>G	XP_011523396.1:p.Thr15Arg
XM_017024914.1:c.44C>G	XP_016880403.1:p.Thr15Arg
XM_017024915.1:c.44C>G	XP_016880404.1:p.Thr15Arg
XM_017024916.1:c.44C>G	XP_016880405.1:p.Thr15Arg
XM_017024917.1:c.44C>G	XP_016880406.1:p.Thr15Arg
XM_017024918.2:c.44C>G	XP_016880407.1:p.Thr15Arg
XM_017024919.1:c.44C>G	XP_016880408.1:p.Thr15Arg
XR_934513.3:n.899C>G
XR_934514.3:n.899C>G
NM_058216.3:c.395C>G MANE Select	NP_478123.1:p.Thr132Arg
NR_103872.2:n.437C>G
NM_002876.4:c.395C>G	NP_002867.1:p.Thr132Arg