Canonical Allele Identifier: CA3057229514

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696747_58696749delinsCGG , CM000679.2:g.58696747_58696749delinsCGG	GRCh38
NC_000017.10:g.56774108_56774110delinsCGG , CM000679.1:g.56774108_56774110delinsCGG	GRCh37
NC_000017.9:g.54129107_54129109delinsCGG	NCBI36
NG_023199.1:g.9146_9148delinsCGG , LRG_314:g.9146_9148delinsCGG
NG_047169.1:g.331_333delinsCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.108_110delinsCGG	ENSP00000464056.2:p.Glu37Gly
ENST00000697675.1:n.3056_3058delinsCGG
ENST00000697676.1:n.519_521delinsCGG
ENST00000697677.1:n.1540_1542delinsCGG
ENST00000697678.1:n.361_363delinsCGG
ENST00000697679.1:n.1533_1535delinsCGG
ENST00000697680.1:c.*1323_*1325delinsCGG	ENSP00000513392.1:n.*1323_*1325delinsCGG
ENST00000697681.1:c.*1350_*1352delinsCGG	ENSP00000513393.1:n.*1350_*1352delinsCGG
ENST00000697683.1:c.*1323_*1325delinsCGG	ENSP00000513395.1:n.*1323_*1325delinsCGG
ENST00000697684.1:n.519_521delinsCGG
ENST00000697685.1:c.*1268+1558_*1268+1560delinsCGG	ENSP00000513396.1:n.*1268+1558_*1268+1560delinsCGG
ENST00000697686.1:c.108_110delinsCGG	ENSP00000513397.1:p.Glu37Gly
ENST00000697687.1:n.450+1558_450+1560delinsCGG
ENST00000697688.1:n.505_507delinsCGG
ENST00000697689.1:c.*1107+1558_*1107+1560delinsCGG	ENSP00000513398.1:n.*1107+1558_*1107+1560delinsCGG
ENST00000697690.1:c.459_461delinsCGG	ENSP00000513399.1:p.Glu154Gly
ENST00000697691.1:c.*431_*433delinsCGG	ENSP00000513400.1:n.*431_*433delinsCGG
ENST00000697692.1:c.*471_*473delinsCGG	ENSP00000513401.1:n.*471_*473delinsCGG
ENST00000697694.1:c.108_110delinsCGG	ENSP00000513402.1:p.Glu37Gly
ENST00000697695.1:n.1066_1068delinsCGG
ENST00000337432.9:c.459_461delinsCGG MANE Select	ENSP00000336701.4:p.Glu154Gly
ENST00000337432.8:c.459_461delinsCGG	ENSP00000336701.4:p.Glu154Gly
ENST00000413590.5:c.97_99delinsCGG
ENST00000425173.5:c.255_257delinsCGG	ENSP00000407282.1:p.Glu86Gly
ENST00000461271.5:c.108_110delinsCGG	ENSP00000464056.1:p.Glu37Gly
ENST00000475762.5:c.*1162_*1164delinsCGG	ENSP00000432421.1:n.*1162_*1164delinsCGG
ENST00000482007.5:c.404+1558_404+1560delinsCGG	ENSP00000433332.1:n.404+1558_404+1560delinsCGG
ENST00000487525.5:c.404+1558_404+1560delinsCGG	ENSP00000431637.1:n.404+1558_404+1560delinsCGG
ENST00000487921.5:n.371_373delinsCGG
ENST00000583539.5:c.459_461delinsCGG	ENSP00000463121.1:p.Glu154Gly
ENST00000584617.5:c.181_183delinsCGG
ENST00000622327.4:c.195_197delinsCGG	ENSP00000482326.1:p.Glu66Gly
NM_058216.2:c.459_461delinsCGG	NP_478123.1:p.Glu154Gly
NR_103872.1:n.475+1558_475+1560delinsCGG
XM_006722001.2:c.459_461delinsCGG	XP_006722064.1:p.Glu154Gly
XM_006722002.2:c.459_461delinsCGG	XP_006722065.1:p.Glu154Gly
XM_006722004.2:c.108_110delinsCGG	XP_006722067.1:p.Glu37Gly
XM_006722005.2:c.108_110delinsCGG	XP_006722068.1:p.Glu37Gly
XM_011525092.1:c.108_110delinsCGG	XP_011523394.1:p.Glu37Gly
XM_011525093.1:c.108_110delinsCGG	XP_011523395.1:p.Glu37Gly
XM_011525094.1:c.108_110delinsCGG	XP_011523396.1:p.Glu37Gly
XR_934513.1:n.532_534delinsCGG
XR_934514.1:n.532_534delinsCGG
XM_006722001.4:c.459_461delinsCGG	XP_006722064.1:p.Glu154Gly
XM_006722002.4:c.459_461delinsCGG	XP_006722065.1:p.Glu154Gly
XM_006722004.3:c.108_110delinsCGG	XP_006722067.1:p.Glu37Gly
XM_006722005.3:c.108_110delinsCGG	XP_006722068.1:p.Glu37Gly
XM_011525092.2:c.108_110delinsCGG	XP_011523394.1:p.Glu37Gly
XM_011525093.2:c.108_110delinsCGG	XP_011523395.1:p.Glu37Gly
XM_011525094.2:c.108_110delinsCGG	XP_011523396.1:p.Glu37Gly
XM_017024914.1:c.108_110delinsCGG	XP_016880403.1:p.Glu37Gly
XM_017024915.1:c.108_110delinsCGG	XP_016880404.1:p.Glu37Gly
XM_017024916.1:c.108_110delinsCGG	XP_016880405.1:p.Glu37Gly
XM_017024917.1:c.108_110delinsCGG	XP_016880406.1:p.Glu37Gly
XM_017024918.2:c.108_110delinsCGG	XP_016880407.1:p.Glu37Gly
XM_017024919.1:c.108_110delinsCGG	XP_016880408.1:p.Glu37Gly
XR_934513.3:n.963_965delinsCGG
XR_934514.3:n.963_965delinsCGG
NM_058216.3:c.459_461delinsCGG MANE Select	NP_478123.1:p.Glu154Gly
NR_103872.2:n.446+1558_446+1560delinsCGG