Canonical Allele Identifier: CA3057229126

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695118_58695120delinsAGC , CM000679.2:g.58695118_58695120delinsAGC	GRCh38
NC_000017.10:g.56772479_56772481delinsAGC , CM000679.1:g.56772479_56772481delinsAGC	GRCh37
NC_000017.9:g.54127478_54127480delinsAGC	NCBI36
NG_023199.1:g.7517_7519delinsAGC , LRG_314:g.7517_7519delinsAGC
NG_047169.1:g.1960_1962delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-19_-17delinsAGC	ENSP00000464056.2:n.-19_-17delinsAGC
ENST00000697675.1:n.1427_1429delinsAGC
ENST00000697676.1:n.393_395delinsAGC
ENST00000697677.1:n.1414_1416delinsAGC
ENST00000697678.1:n.235_237delinsAGC
ENST00000697679.1:n.1407_1409delinsAGC
ENST00000697680.1:c.*1197_*1199delinsAGC	ENSP00000513392.1:n.*1197_*1199delinsAGC
ENST00000697681.1:c.*1197_*1199delinsAGC	ENSP00000513393.1:n.*1197_*1199delinsAGC
ENST00000697683.1:c.*1197_*1199delinsAGC	ENSP00000513395.1:n.*1197_*1199delinsAGC
ENST00000697684.1:n.393_395delinsAGC
ENST00000697685.1:c.*1197_*1199delinsAGC	ENSP00000513396.1:n.*1197_*1199delinsAGC
ENST00000697686.1:c.-19_-17delinsAGC	ENSP00000513397.1:n.-19_-17delinsAGC
ENST00000697687.1:n.379_381delinsAGC
ENST00000697688.1:n.379_381delinsAGC
ENST00000697689.1:c.*1036_*1038delinsAGC	ENSP00000513398.1:n.*1036_*1038delinsAGC
ENST00000697690.1:c.333_335delinsAGC	ENSP00000513399.1:p.Gly112Ala
ENST00000697691.1:c.*305_*307delinsAGC	ENSP00000513400.1:n.*305_*307delinsAGC
ENST00000697692.1:c.*345_*347delinsAGC	ENSP00000513401.1:n.*345_*347delinsAGC
ENST00000697693.1:n.1108_1110delinsAGC
ENST00000697694.1:c.-19_-17delinsAGC	ENSP00000513402.1:n.-19_-17delinsAGC
ENST00000697695.1:n.940_942delinsAGC
ENST00000337432.9:c.333_335delinsAGC MANE Select	ENSP00000336701.4:p.Gly112Ala
ENST00000337432.8:c.333_335delinsAGC	ENSP00000336701.4:p.Gly112Ala
ENST00000421782.3:c.333_335delinsAGC	ENSP00000391450.2:p.Gly112Ala
ENST00000425173.5:c.129_131delinsAGC	ENSP00000407282.1:p.Gly44Ala
ENST00000461271.5:c.-19_-17delinsAGC	ENSP00000464056.1:n.-19_-17delinsAGC
ENST00000475762.5:c.*1036_*1038delinsAGC	ENSP00000432421.1:n.*1036_*1038delinsAGC
ENST00000482007.5:c.333_335delinsAGC	ENSP00000433332.1:p.Gly112Ala
ENST00000486827.1:c.*1197_*1199delinsAGC	ENSP00000436761.1:n.*1197_*1199delinsAGC
ENST00000487525.5:c.333_335delinsAGC	ENSP00000431637.1:p.Gly112Ala
ENST00000487921.5:n.245_247delinsAGC
ENST00000583539.5:c.333_335delinsAGC	ENSP00000463121.1:p.Gly112Ala
ENST00000584617.5:c.127-1575_127-1573delinsAGC
ENST00000622327.4:c.69_71delinsAGC	ENSP00000482326.1:p.Gly24Ala
NM_002876.3:c.333_335delinsAGC	NP_002867.1:p.Gly112Ala
NM_058216.2:c.333_335delinsAGC	NP_478123.1:p.Gly112Ala
NR_103872.1:n.404_406delinsAGC
NR_103873.1:n.301_303delinsAGC
XM_006722001.2:c.333_335delinsAGC	XP_006722064.1:p.Gly112Ala
XM_006722002.2:c.333_335delinsAGC	XP_006722065.1:p.Gly112Ala
XM_006722004.2:c.-19_-17delinsAGC	XP_006722067.1:n.-19_-17delinsAGC
XM_006722005.2:c.-19_-17delinsAGC	XP_006722068.1:n.-19_-17delinsAGC
XM_011525092.1:c.-19_-17delinsAGC	XP_011523394.1:n.-19_-17delinsAGC
XM_011525093.1:c.-19_-17delinsAGC	XP_011523395.1:n.-19_-17delinsAGC
XM_011525094.1:c.-19_-17delinsAGC	XP_011523396.1:n.-19_-17delinsAGC
XR_934513.1:n.406_408delinsAGC
XR_934514.1:n.406_408delinsAGC
XM_006722001.4:c.333_335delinsAGC	XP_006722064.1:p.Gly112Ala
XM_006722002.4:c.333_335delinsAGC	XP_006722065.1:p.Gly112Ala
XM_006722004.3:c.-19_-17delinsAGC	XP_006722067.1:n.-19_-17delinsAGC
XM_006722005.3:c.-19_-17delinsAGC	XP_006722068.1:n.-19_-17delinsAGC
XM_011525092.2:c.-19_-17delinsAGC	XP_011523394.1:n.-19_-17delinsAGC
XM_011525093.2:c.-19_-17delinsAGC	XP_011523395.1:n.-19_-17delinsAGC
XM_011525094.2:c.-19_-17delinsAGC	XP_011523396.1:n.-19_-17delinsAGC
XM_017024914.1:c.-19_-17delinsAGC	XP_016880403.1:n.-19_-17delinsAGC
XM_017024915.1:c.-19_-17delinsAGC	XP_016880404.1:n.-19_-17delinsAGC
XM_017024916.1:c.-19_-17delinsAGC	XP_016880405.1:n.-19_-17delinsAGC
XM_017024917.1:c.-19_-17delinsAGC	XP_016880406.1:n.-19_-17delinsAGC
XM_017024918.2:c.-19_-17delinsAGC	XP_016880407.1:n.-19_-17delinsAGC
XM_017024919.1:c.-19_-17delinsAGC	XP_016880408.1:n.-19_-17delinsAGC
XR_934513.3:n.837_839delinsAGC
XR_934514.3:n.837_839delinsAGC
NM_058216.3:c.333_335delinsAGC MANE Select	NP_478123.1:p.Gly112Ala
NR_103872.2:n.375_377delinsAGC
NM_002876.4:c.333_335delinsAGC	NP_002867.1:p.Gly112Ala