Canonical Allele Identifier: CA2267815383

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695190_58695195delinsGTAAAA , CM000679.2:g.58695190_58695195delinsGTAAAA	GRCh38
NC_000017.10:g.56772551_56772556delinsGTAAAA , CM000679.1:g.56772551_56772556delinsGTAAAA	GRCh37
NC_000017.9:g.54127550_54127555delinsGTAAAA	NCBI36
NG_023199.1:g.7589_7594delinsGTAAAA , LRG_314:g.7589_7594delinsGTAAAA
NG_047169.1:g.1885_1890delinsTTTTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.53+1_53+6delinsGTAAAA	ENSP00000464056.2:n.53+1_53+6delinsGTAAAA
ENST00000697675.1:n.1499_1504delinsGTAAAA
ENST00000697676.1:n.464+1_464+6delinsGTAAAA
ENST00000697677.1:n.1485+1_1485+6delinsGTAAAA
ENST00000697678.1:n.306+1_306+6delinsGTAAAA
ENST00000697679.1:n.1478+1_1478+6delinsGTAAAA
ENST00000697680.1:c.*1268+1_*1268+6delinsGTAAAA	ENSP00000513392.1:n.*1268+1_*1268+6delinsGTAAAA
ENST00000697681.1:c.*1269_*1274delinsGTAAAA	ENSP00000513393.1:n.*1269_*1274delinsGTAAAA
ENST00000697683.1:c.*1268+1_*1268+6delinsGTAAAA	ENSP00000513395.1:n.*1268+1_*1268+6delinsGTAAAA
ENST00000697684.1:n.464+1_464+6delinsGTAAAA
ENST00000697685.1:c.*1268+1_*1268+6delinsGTAAAA	ENSP00000513396.1:n.*1268+1_*1268+6delinsGTAAAA
ENST00000697686.1:c.53+1_53+6delinsGTAAAA	ENSP00000513397.1:n.53+1_53+6delinsGTAAAA
ENST00000697687.1:n.450+1_450+6delinsGTAAAA
ENST00000697688.1:n.450+1_450+6delinsGTAAAA
ENST00000697689.1:c.*1107+1_*1107+6delinsGTAAAA	ENSP00000513398.1:n.*1107+1_*1107+6delinsGTAAAA
ENST00000697690.1:c.404+1_404+6delinsGTAAAA	ENSP00000513399.1:n.404+1_404+6delinsGTAAAA
ENST00000697691.1:c.*376+1_*376+6delinsGTAAAA	ENSP00000513400.1:n.*376+1_*376+6delinsGTAAAA
ENST00000697692.1:c.*416+1_*416+6delinsGTAAAA	ENSP00000513401.1:n.*416+1_*416+6delinsGTAAAA
ENST00000697693.1:n.1180_1185delinsGTAAAA
ENST00000697694.1:c.53+1_53+6delinsGTAAAA	ENSP00000513402.1:n.53+1_53+6delinsGTAAAA
ENST00000697695.1:n.1011+1_1011+6delinsGTAAAA
ENST00000337432.9:c.404+1_404+6delinsGTAAAA MANE Select	ENSP00000336701.4:n.404+1_404+6delinsGTAAAA
ENST00000337432.8:c.404+1_404+6delinsGTAAAA	ENSP00000336701.4:n.404+1_404+6delinsGTAAAA
ENST00000413590.5:c.42+1_42+6delinsGTAAAA
ENST00000421782.3:c.405_*2delinsGTAAAA	ENSP00000391450.2:n.[c.405_*2delinsGTAAAA;Trp135=]
ENST00000425173.5:c.200+1_200+6delinsGTAAAA	ENSP00000407282.1:n.200+1_200+6delinsGTAAAA
ENST00000461271.5:c.53+1_53+6delinsGTAAAA	ENSP00000464056.1:n.53+1_53+6delinsGTAAAA
ENST00000475762.5:c.*1107+1_*1107+6delinsGTAAAA	ENSP00000432421.1:n.*1107+1_*1107+6delinsGTAAAA
ENST00000482007.5:c.404+1_404+6delinsGTAAAA	ENSP00000433332.1:n.404+1_404+6delinsGTAAAA
ENST00000486827.1:c.*1269_*1274delinsGTAAAA	ENSP00000436761.1:n.*1269_*1274delinsGTAAAA
ENST00000487525.5:c.404+1_404+6delinsGTAAAA	ENSP00000431637.1:n.404+1_404+6delinsGTAAAA
ENST00000487921.5:n.316+1_316+6delinsGTAAAA
ENST00000583539.5:c.404+1_404+6delinsGTAAAA	ENSP00000463121.1:n.404+1_404+6delinsGTAAAA
ENST00000584617.5:c.127-1503_127-1498delinsGTAAAA
ENST00000622327.4:c.140+1_140+6delinsGTAAAA	ENSP00000482326.1:n.140+1_140+6delinsGTAAAA
NM_002876.3:c.405_*2delinsGTAAAA	NP_002867.1:n.[c.405_*2delinsGTAAAA;Trp135=]
NM_058216.2:c.404+1_404+6delinsGTAAAA	NP_478123.1:n.404+1_404+6delinsGTAAAA
NR_103872.1:n.475+1_475+6delinsGTAAAA
NR_103873.1:n.373_378delinsGTAAAA
XM_006722001.2:c.404+1_404+6delinsGTAAAA	XP_006722064.1:n.404+1_404+6delinsGTAAAA
XM_006722002.2:c.404+1_404+6delinsGTAAAA	XP_006722065.1:n.404+1_404+6delinsGTAAAA
XM_006722004.2:c.53+1_53+6delinsGTAAAA	XP_006722067.1:n.53+1_53+6delinsGTAAAA
XM_006722005.2:c.53+1_53+6delinsGTAAAA	XP_006722068.1:n.53+1_53+6delinsGTAAAA
XM_011525092.1:c.53+1_53+6delinsGTAAAA	XP_011523394.1:n.53+1_53+6delinsGTAAAA
XM_011525093.1:c.53+1_53+6delinsGTAAAA	XP_011523395.1:n.53+1_53+6delinsGTAAAA
XM_011525094.1:c.53+1_53+6delinsGTAAAA	XP_011523396.1:n.53+1_53+6delinsGTAAAA
XR_934513.1:n.477+1_477+6delinsGTAAAA
XR_934514.1:n.477+1_477+6delinsGTAAAA
XM_006722001.4:c.404+1_404+6delinsGTAAAA	XP_006722064.1:n.404+1_404+6delinsGTAAAA
XM_006722002.4:c.404+1_404+6delinsGTAAAA	XP_006722065.1:n.404+1_404+6delinsGTAAAA
XM_006722004.3:c.53+1_53+6delinsGTAAAA	XP_006722067.1:n.53+1_53+6delinsGTAAAA
XM_006722005.3:c.53+1_53+6delinsGTAAAA	XP_006722068.1:n.53+1_53+6delinsGTAAAA
XM_011525092.2:c.53+1_53+6delinsGTAAAA	XP_011523394.1:n.53+1_53+6delinsGTAAAA
XM_011525093.2:c.53+1_53+6delinsGTAAAA	XP_011523395.1:n.53+1_53+6delinsGTAAAA
XM_011525094.2:c.53+1_53+6delinsGTAAAA	XP_011523396.1:n.53+1_53+6delinsGTAAAA
XM_017024914.1:c.53+1_53+6delinsGTAAAA	XP_016880403.1:n.53+1_53+6delinsGTAAAA
XM_017024915.1:c.53+1_53+6delinsGTAAAA	XP_016880404.1:n.53+1_53+6delinsGTAAAA
XM_017024916.1:c.53+1_53+6delinsGTAAAA	XP_016880405.1:n.53+1_53+6delinsGTAAAA
XM_017024917.1:c.53+1_53+6delinsGTAAAA	XP_016880406.1:n.53+1_53+6delinsGTAAAA
XM_017024918.2:c.53+1_53+6delinsGTAAAA	XP_016880407.1:n.53+1_53+6delinsGTAAAA
XM_017024919.1:c.53+1_53+6delinsGTAAAA	XP_016880408.1:n.53+1_53+6delinsGTAAAA
XR_934513.3:n.908+1_908+6delinsGTAAAA
XR_934514.3:n.908+1_908+6delinsGTAAAA
NM_058216.3:c.404+1_404+6delinsGTAAAA MANE Select	NP_478123.1:n.404+1_404+6delinsGTAAAA
NR_103872.2:n.446+1_446+6delinsGTAAAA
NM_002876.4:c.405_*2delinsGTAAAA	NP_002867.1:n.[c.405_*2delinsGTAAAA;Trp135=]