Canonical Allele Identifier: CA2838032138

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696824_58696832dup , CM000679.2:g.58696824_58696832dup	GRCh38
NC_000017.10:g.56774185_56774193dup , CM000679.1:g.56774185_56774193dup	GRCh37
NC_000017.9:g.54129184_54129192dup	NCBI36
NG_023199.1:g.9223_9231dup , LRG_314:g.9223_9231dup
NG_047169.1:g.254_262dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.185_193dup	ENSP00000464056.2:p.Gln64_Leu65insHisLeuGln
ENST00000697675.1:n.3133_3141dup
ENST00000697676.1:n.596_604dup
ENST00000697677.1:n.1617_1625dup
ENST00000697678.1:n.438_446dup
ENST00000697679.1:n.1610_1618dup
ENST00000697680.1:c.*1400_*1408dup	ENSP00000513392.1:n.*1400_*1408dup
ENST00000697681.1:c.*1427_*1435dup	ENSP00000513393.1:n.*1427_*1435dup
ENST00000697683.1:c.*1400_*1408dup	ENSP00000513395.1:n.*1400_*1408dup
ENST00000697684.1:n.596_604dup
ENST00000697685.1:c.*1268+1635_*1268+1643dup	ENSP00000513396.1:n.*1268+1635_*1268+1643dup
ENST00000697686.1:c.185_193dup	ENSP00000513397.1:p.Gln64_Leu65insHisLeuGln
ENST00000697687.1:n.450+1635_450+1643dup
ENST00000697688.1:n.582_590dup
ENST00000697689.1:c.*1107+1635_*1107+1643dup	ENSP00000513398.1:n.*1107+1635_*1107+1643dup
ENST00000697690.1:c.536_544dup	ENSP00000513399.1:p.Gln181_Leu182insHisLeuGln
ENST00000697691.1:c.*508_*516dup	ENSP00000513400.1:n.*508_*516dup
ENST00000697692.1:c.*548_*556dup	ENSP00000513401.1:n.*548_*556dup
ENST00000697694.1:c.185_193dup	ENSP00000513402.1:p.Gln64_Leu65insHisLeuGln
ENST00000697695.1:n.1143_1151dup
ENST00000337432.9:c.536_544dup MANE Select	ENSP00000336701.4:p.Gln181_Leu182insHisLeuGln
ENST00000337432.8:c.536_544dup	ENSP00000336701.4:p.Gln181_Leu182insHisLeuGln
ENST00000413590.5:c.174_182dup
ENST00000425173.5:c.332_340dup	ENSP00000407282.1:p.Gln113_Leu114insHisLeuGln
ENST00000461271.5:c.185_193dup	ENSP00000464056.1:p.Gln64_Leu65insHisLeuGln
ENST00000475762.5:c.*1239_*1247dup	ENSP00000432421.1:n.*1239_*1247dup
ENST00000482007.5:c.404+1635_404+1643dup	ENSP00000433332.1:n.404+1635_404+1643dup
ENST00000487525.5:c.404+1635_404+1643dup	ENSP00000431637.1:n.404+1635_404+1643dup
ENST00000487921.5:n.448_456dup
ENST00000583539.5:c.536_544dup	ENSP00000463121.1:p.Gln181_Leu182insHisLeuGln
ENST00000584617.5:c.258_266dup
ENST00000622327.4:c.272_280dup	ENSP00000482326.1:p.Gln93_Leu94insHisLeuGln
NM_058216.2:c.536_544dup	NP_478123.1:p.Gln181_Leu182insHisLeuGln
NR_103872.1:n.475+1635_475+1643dup
XM_006722001.2:c.536_544dup	XP_006722064.1:p.Gln181_Leu182insHisLeuGln
XM_006722002.2:c.536_544dup	XP_006722065.1:p.Gln181_Leu182insHisLeuGln
XM_006722004.2:c.185_193dup	XP_006722067.1:p.Gln64_Leu65insHisLeuGln
XM_006722005.2:c.185_193dup	XP_006722068.1:p.Gln64_Leu65insHisLeuGln
XM_011525092.1:c.185_193dup	XP_011523394.1:p.Gln64_Leu65insHisLeuGln
XM_011525093.1:c.185_193dup	XP_011523395.1:p.Gln64_Leu65insHisLeuGln
XM_011525094.1:c.185_193dup	XP_011523396.1:p.Gln64_Leu65insHisLeuGln
XR_934513.1:n.609_617dup
XR_934514.1:n.609_617dup
XM_006722001.4:c.536_544dup	XP_006722064.1:p.Gln181_Leu182insHisLeuGln
XM_006722002.4:c.536_544dup	XP_006722065.1:p.Gln181_Leu182insHisLeuGln
XM_006722004.3:c.185_193dup	XP_006722067.1:p.Gln64_Leu65insHisLeuGln
XM_006722005.3:c.185_193dup	XP_006722068.1:p.Gln64_Leu65insHisLeuGln
XM_011525092.2:c.185_193dup	XP_011523394.1:p.Gln64_Leu65insHisLeuGln
XM_011525093.2:c.185_193dup	XP_011523395.1:p.Gln64_Leu65insHisLeuGln
XM_011525094.2:c.185_193dup	XP_011523396.1:p.Gln64_Leu65insHisLeuGln
XM_017024914.1:c.185_193dup	XP_016880403.1:p.Gln64_Leu65insHisLeuGln
XM_017024915.1:c.185_193dup	XP_016880404.1:p.Gln64_Leu65insHisLeuGln
XM_017024916.1:c.185_193dup	XP_016880405.1:p.Gln64_Leu65insHisLeuGln
XM_017024917.1:c.185_193dup	XP_016880406.1:p.Gln64_Leu65insHisLeuGln
XM_017024918.2:c.185_193dup	XP_016880407.1:p.Gln64_Leu65insHisLeuGln
XM_017024919.1:c.185_193dup	XP_016880408.1:p.Gln64_Leu65insHisLeuGln
XR_934513.3:n.1040_1048dup
XR_934514.3:n.1040_1048dup
NM_058216.3:c.536_544dup MANE Select	NP_478123.1:p.Gln181_Leu182insHisLeuGln
NR_103872.2:n.446+1635_446+1643dup