Canonical Allele Identifier: CA3057242389
Community Standard Title: NM_058216.3(RAD51C):c.549_550delinsCA (p.Ala184Thr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696837_58696838delinsCA , CM000679.2:g.58696837_58696838delinsCA GRCh38
NC_000017.10:g.56774198_56774199delinsCA , CM000679.1:g.56774198_56774199delinsCA GRCh37
NC_000017.9:g.54129197_54129198delinsCA NCBI36
NG_023199.1:g.9236_9237delinsCA , LRG_314:g.9236_9237delinsCA
NG_047169.1:g.242_243delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.549_550delinsCA MANE Select NP_478123.1:p.Ala184Thr
ENST00000337432.9:c.549_550delinsCA MANE Select ENSP00000336701.4:p.Ala184Thr
NM_058216.2:c.549_550delinsCA NP_478123.1:p.Ala184Thr
NR_103872.1:n.475+1648_475+1649delinsCA
NR_103872.2:n.446+1648_446+1649delinsCA
ENST00000337432.8:c.549_550delinsCA ENSP00000336701.4:p.Ala184Thr
ENST00000413590.5:c.187_188delinsCA
ENST00000425173.5:c.345_346delinsCA ENSP00000407282.1:p.Ala116Thr
ENST00000461271.5:c.198_199delinsCA ENSP00000464056.1:p.Ala67Thr
ENST00000461271.6:c.198_199delinsCA ENSP00000464056.2:p.Ala67Thr
ENST00000475762.5:c.*1252_*1253delinsCA ENSP00000432421.1:n.*1252_*1253delinsCA
ENST00000482007.5:c.404+1648_404+1649delinsCA ENSP00000433332.1:n.404+1648_404+1649delinsCA
ENST00000487525.5:c.404+1648_404+1649delinsCA ENSP00000431637.1:n.404+1648_404+1649delinsCA
ENST00000487921.5:n.461_462delinsCA
ENST00000583539.5:c.549_550delinsCA ENSP00000463121.1:p.Ala184Thr
ENST00000584617.5:c.271_272delinsCA
ENST00000622327.4:c.285_286delinsCA ENSP00000482326.1:p.Ala96Thr
ENST00000697675.1:n.3146_3147delinsCA
ENST00000697676.1:n.609_610delinsCA
ENST00000697677.1:n.1630_1631delinsCA
ENST00000697678.1:n.451_452delinsCA
ENST00000697679.1:n.1623_1624delinsCA
ENST00000697680.1:c.*1413_*1414delinsCA ENSP00000513392.1:n.*1413_*1414delinsCA
ENST00000697681.1:c.*1440_*1441delinsCA ENSP00000513393.1:n.*1440_*1441delinsCA
ENST00000697683.1:c.*1413_*1414delinsCA ENSP00000513395.1:n.*1413_*1414delinsCA
ENST00000697684.1:n.609_610delinsCA
ENST00000697685.1:c.*1268+1648_*1268+1649delinsCA ENSP00000513396.1:n.*1268+1648_*1268+1649delinsCA
ENST00000697686.1:c.198_199delinsCA ENSP00000513397.1:p.Ala67Thr
ENST00000697687.1:n.450+1648_450+1649delinsCA
ENST00000697688.1:n.595_596delinsCA
ENST00000697689.1:c.*1107+1648_*1107+1649delinsCA ENSP00000513398.1:n.*1107+1648_*1107+1649delinsCA
ENST00000697690.1:c.549_550delinsCA ENSP00000513399.1:p.Ala184Thr
ENST00000697691.1:c.*521_*522delinsCA ENSP00000513400.1:n.*521_*522delinsCA
ENST00000697692.1:c.*561_*562delinsCA ENSP00000513401.1:n.*561_*562delinsCA
ENST00000697694.1:c.198_199delinsCA ENSP00000513402.1:p.Ala67Thr
ENST00000697695.1:n.1156_1157delinsCA
XM_006722001.2:c.549_550delinsCA XP_006722064.1:p.Ala184Thr
XM_006722001.4:c.549_550delinsCA XP_006722064.1:p.Ala184Thr
XM_006722002.2:c.549_550delinsCA XP_006722065.1:p.Ala184Thr
XM_006722002.4:c.549_550delinsCA XP_006722065.1:p.Ala184Thr
XM_006722004.2:c.198_199delinsCA XP_006722067.1:p.Ala67Thr
XM_006722004.3:c.198_199delinsCA XP_006722067.1:p.Ala67Thr
XM_006722005.2:c.198_199delinsCA XP_006722068.1:p.Ala67Thr
XM_006722005.3:c.198_199delinsCA XP_006722068.1:p.Ala67Thr
XM_011525092.1:c.198_199delinsCA XP_011523394.1:p.Ala67Thr
XM_011525092.2:c.198_199delinsCA XP_011523394.1:p.Ala67Thr
XM_011525093.1:c.198_199delinsCA XP_011523395.1:p.Ala67Thr
XM_011525093.2:c.198_199delinsCA XP_011523395.1:p.Ala67Thr
XM_011525094.1:c.198_199delinsCA XP_011523396.1:p.Ala67Thr
XM_011525094.2:c.198_199delinsCA XP_011523396.1:p.Ala67Thr
XM_017024914.1:c.198_199delinsCA XP_016880403.1:p.Ala67Thr
XM_017024915.1:c.198_199delinsCA XP_016880404.1:p.Ala67Thr
XM_017024916.1:c.198_199delinsCA XP_016880405.1:p.Ala67Thr
XM_017024917.1:c.198_199delinsCA XP_016880406.1:p.Ala67Thr
XM_017024918.2:c.198_199delinsCA XP_016880407.1:p.Ala67Thr
XM_017024919.1:c.198_199delinsCA XP_016880408.1:p.Ala67Thr
XR_934513.1:n.622_623delinsCA
XR_934513.3:n.1053_1054delinsCA
XR_934514.1:n.622_623delinsCA
XR_934514.3:n.1053_1054delinsCA