Canonical Allele Identifier: CA2267816245

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696822_58696823delinsGC , CM000679.2:g.58696822_58696823delinsGC	GRCh38
NC_000017.10:g.56774183_56774184delinsGC , CM000679.1:g.56774183_56774184delinsGC	GRCh37
NC_000017.9:g.54129182_54129183delinsGC	NCBI36
NG_023199.1:g.9221_9222delinsGC , LRG_314:g.9221_9222delinsGC
NG_047169.1:g.257_258delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.183_184delinsGC	ENSP00000464056.2:p.Gln61=
ENST00000697675.1:n.3131_3132delinsGC
ENST00000697676.1:n.594_595delinsGC
ENST00000697677.1:n.1615_1616delinsGC
ENST00000697678.1:n.436_437delinsGC
ENST00000697679.1:n.1608_1609delinsGC
ENST00000697680.1:c.*1398_*1399delinsGC	ENSP00000513392.1:n.*1398_*1399delinsGC
ENST00000697681.1:c.*1425_*1426delinsGC	ENSP00000513393.1:n.*1425_*1426delinsGC
ENST00000697683.1:c.*1398_*1399delinsGC	ENSP00000513395.1:n.*1398_*1399delinsGC
ENST00000697684.1:n.594_595delinsGC
ENST00000697685.1:c.*1268+1633_*1268+1634delinsGC	ENSP00000513396.1:n.*1268+1633_*1268+1634...
ENST00000697686.1:c.183_184delinsGC	ENSP00000513397.1:p.Gln61=
ENST00000697687.1:n.450+1633_450+1634delinsGC
ENST00000697688.1:n.580_581delinsGC
ENST00000697689.1:c.*1107+1633_*1107+1634delinsGC	ENSP00000513398.1:n.*1107+1633_*1107+1634...
ENST00000697690.1:c.534_535delinsGC	ENSP00000513399.1:p.Gln178=
ENST00000697691.1:c.*506_*507delinsGC	ENSP00000513400.1:n.*506_*507delinsGC
ENST00000697692.1:c.*546_*547delinsGC	ENSP00000513401.1:n.*546_*547delinsGC
ENST00000697694.1:c.183_184delinsGC	ENSP00000513402.1:p.Gln61=
ENST00000697695.1:n.1141_1142delinsGC
ENST00000337432.9:c.534_535delinsGC MANE Select	ENSP00000336701.4:p.Gln178=
ENST00000337432.8:c.534_535delinsGC	ENSP00000336701.4:p.Gln178=
ENST00000413590.5:c.172_173delinsGC
ENST00000425173.5:c.330_331delinsGC	ENSP00000407282.1:p.Gln110=
ENST00000461271.5:c.183_184delinsGC	ENSP00000464056.1:p.Gln61=
ENST00000475762.5:c.*1237_*1238delinsGC	ENSP00000432421.1:n.*1237_*1238delinsGC
ENST00000482007.5:c.404+1633_404+1634delinsGC	ENSP00000433332.1:n.404+1633_404+1634deli...
ENST00000487525.5:c.404+1633_404+1634delinsGC	ENSP00000431637.1:n.404+1633_404+1634deli...
ENST00000487921.5:n.446_447delinsGC
ENST00000583539.5:c.534_535delinsGC	ENSP00000463121.1:p.Gln178=
ENST00000584617.5:c.256_257delinsGC
ENST00000622327.4:c.270_271delinsGC	ENSP00000482326.1:p.Gln90=
NM_058216.2:c.534_535delinsGC	NP_478123.1:p.Gln178=
NR_103872.1:n.475+1633_475+1634delinsGC
XM_006722001.2:c.534_535delinsGC	XP_006722064.1:p.Gln178=
XM_006722002.2:c.534_535delinsGC	XP_006722065.1:p.Gln178=
XM_006722004.2:c.183_184delinsGC	XP_006722067.1:p.Gln61=
XM_006722005.2:c.183_184delinsGC	XP_006722068.1:p.Gln61=
XM_011525092.1:c.183_184delinsGC	XP_011523394.1:p.Gln61=
XM_011525093.1:c.183_184delinsGC	XP_011523395.1:p.Gln61=
XM_011525094.1:c.183_184delinsGC	XP_011523396.1:p.Gln61=
XR_934513.1:n.607_608delinsGC
XR_934514.1:n.607_608delinsGC
XM_006722001.4:c.534_535delinsGC	XP_006722064.1:p.Gln178=
XM_006722002.4:c.534_535delinsGC	XP_006722065.1:p.Gln178=
XM_006722004.3:c.183_184delinsGC	XP_006722067.1:p.Gln61=
XM_006722005.3:c.183_184delinsGC	XP_006722068.1:p.Gln61=
XM_011525092.2:c.183_184delinsGC	XP_011523394.1:p.Gln61=
XM_011525093.2:c.183_184delinsGC	XP_011523395.1:p.Gln61=
XM_011525094.2:c.183_184delinsGC	XP_011523396.1:p.Gln61=
XM_017024914.1:c.183_184delinsGC	XP_016880403.1:p.Gln61=
XM_017024915.1:c.183_184delinsGC	XP_016880404.1:p.Gln61=
XM_017024916.1:c.183_184delinsGC	XP_016880405.1:p.Gln61=
XM_017024917.1:c.183_184delinsGC	XP_016880406.1:p.Gln61=
XM_017024918.2:c.183_184delinsGC	XP_016880407.1:p.Gln61=
XM_017024919.1:c.183_184delinsGC	XP_016880408.1:p.Gln61=
XR_934513.3:n.1038_1039delinsGC
XR_934514.3:n.1038_1039delinsGC
NM_058216.3:c.534_535delinsGC MANE Select	NP_478123.1:p.Gln178=
NR_103872.2:n.446+1633_446+1634delinsGC