Canonical Allele Identifier: CA916081893

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 860928
• ClinVar RCV Id: RCV001067329 ; RCV001271005 ; RCV002290581 ; RCV002355089
• dbSNP Id: rs2047958236

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695164_58695165insG , CM000679.2:g.58695164_58695165insG	GRCh38
NC_000017.10:g.56772525_56772526insG , CM000679.1:g.56772525_56772526insG	GRCh37
NC_000017.9:g.54127524_54127525insG	NCBI36
NG_023199.1:g.7563_7564insG , LRG_314:g.7563_7564insG
NG_047169.1:g.1915_1916insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.28_29insG	ENSP00000464056.2:p.Pro10ArgfsTer28
ENST00000697675.1:n.1473_1474insG
ENST00000697676.1:n.439_440insG
ENST00000697677.1:n.1460_1461insG
ENST00000697678.1:n.281_282insG
ENST00000697679.1:n.1453_1454insG
ENST00000697680.1:c.*1243_*1244insG	ENSP00000513392.1:n.*1243_*1244insG
ENST00000697681.1:c.*1243_*1244insG	ENSP00000513393.1:n.*1243_*1244insG
ENST00000697683.1:c.*1243_*1244insG	ENSP00000513395.1:n.*1243_*1244insG
ENST00000697684.1:n.439_440insG
ENST00000697685.1:c.*1243_*1244insG	ENSP00000513396.1:n.*1243_*1244insG
ENST00000697686.1:c.28_29insG	ENSP00000513397.1:p.Pro10ArgfsTer28
ENST00000697687.1:n.425_426insG
ENST00000697688.1:n.425_426insG
ENST00000697689.1:c.*1082_*1083insG	ENSP00000513398.1:n.*1082_*1083insG
ENST00000697690.1:c.379_380insG	ENSP00000513399.1:p.Pro127ArgfsTer28
ENST00000697691.1:c.*351_*352insG	ENSP00000513400.1:n.*351_*352insG
ENST00000697692.1:c.*391_*392insG	ENSP00000513401.1:n.*391_*392insG
ENST00000697693.1:n.1154_1155insG
ENST00000697694.1:c.28_29insG	ENSP00000513402.1:p.Pro10ArgfsTer28
ENST00000697695.1:n.986_987insG
ENST00000337432.9:c.379_380insG MANE Select	ENSP00000336701.4:p.Pro127ArgfsTer28
ENST00000337432.8:c.379_380insG	ENSP00000336701.4:p.Pro127ArgfsTer28
ENST00000413590.5:c.17_18insG
ENST00000421782.3:c.379_380insG	ENSP00000391450.2:p.Pro127ArgfsTer12
ENST00000425173.5:c.175_176insG	ENSP00000407282.1:p.Pro59ArgfsTer28
ENST00000461271.5:c.28_29insG	ENSP00000464056.1:p.Pro10ArgfsTer28
ENST00000475762.5:c.*1082_*1083insG	ENSP00000432421.1:n.*1082_*1083insG
ENST00000482007.5:c.379_380insG	ENSP00000433332.1:p.Pro127ArgfsTer?
ENST00000486827.1:c.*1243_*1244insG	ENSP00000436761.1:n.*1243_*1244insG
ENST00000487525.5:c.379_380insG	ENSP00000431637.1:p.Pro127ArgfsTer?
ENST00000487921.5:n.291_292insG
ENST00000583539.5:c.379_380insG	ENSP00000463121.1:p.Pro127ArgfsTer28
ENST00000584617.5:c.127-1529_127-1528insG
ENST00000622327.4:c.115_116insG	ENSP00000482326.1:p.Pro39ArgfsTer28
NM_002876.3:c.379_380insG	NP_002867.1:p.Pro127ArgfsTer12
NM_058216.2:c.379_380insG	NP_478123.1:p.Pro127ArgfsTer28
NR_103872.1:n.450_451insG
NR_103873.1:n.347_348insG
XM_006722001.2:c.379_380insG	XP_006722064.1:p.Pro127ArgfsTer28
XM_006722002.2:c.379_380insG	XP_006722065.1:p.Pro127ArgfsTer28
XM_006722004.2:c.28_29insG	XP_006722067.1:p.Pro10ArgfsTer28
XM_006722005.2:c.28_29insG	XP_006722068.1:p.Pro10ArgfsTer28
XM_011525092.1:c.28_29insG	XP_011523394.1:p.Pro10ArgfsTer28
XM_011525093.1:c.28_29insG	XP_011523395.1:p.Pro10ArgfsTer28
XM_011525094.1:c.28_29insG	XP_011523396.1:p.Pro10ArgfsTer28
XR_934513.1:n.452_453insG
XR_934514.1:n.452_453insG
XM_006722001.4:c.379_380insG	XP_006722064.1:p.Pro127ArgfsTer28
XM_006722002.4:c.379_380insG	XP_006722065.1:p.Pro127ArgfsTer28
XM_006722004.3:c.28_29insG	XP_006722067.1:p.Pro10ArgfsTer28
XM_006722005.3:c.28_29insG	XP_006722068.1:p.Pro10ArgfsTer28
XM_011525092.2:c.28_29insG	XP_011523394.1:p.Pro10ArgfsTer28
XM_011525093.2:c.28_29insG	XP_011523395.1:p.Pro10ArgfsTer28
XM_011525094.2:c.28_29insG	XP_011523396.1:p.Pro10ArgfsTer28
XM_017024914.1:c.28_29insG	XP_016880403.1:p.Pro10ArgfsTer28
XM_017024915.1:c.28_29insG	XP_016880404.1:p.Pro10ArgfsTer28
XM_017024916.1:c.28_29insG	XP_016880405.1:p.Pro10ArgfsTer28
XM_017024917.1:c.28_29insG	XP_016880406.1:p.Pro10ArgfsTer28
XM_017024918.2:c.28_29insG	XP_016880407.1:p.Pro10ArgfsTer28
XM_017024919.1:c.28_29insG	XP_016880408.1:p.Pro10ArgfsTer28
XR_934513.3:n.883_884insG
XR_934514.3:n.883_884insG
NM_058216.3:c.379_380insG MANE Select	NP_478123.1:p.Pro127ArgfsTer28
NR_103872.2:n.421_422insG
NM_002876.4:c.379_380insG	NP_002867.1:p.Pro127ArgfsTer12