Canonical Allele Identifier: CA3261180171
Community Standard Title: NM_058216.3(RAD51C):c.679_681delinsAGC (p.Pro227Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703303_58703305delinsAGC , CM000679.2:g.58703303_58703305delinsAGC GRCh38
NC_000017.10:g.56780664_56780666delinsAGC , CM000679.1:g.56780664_56780666delinsAGC GRCh37
NC_000017.9:g.54135663_54135665delinsAGC NCBI36
NG_023199.1:g.15702_15704delinsAGC , LRG_314:g.15702_15704delinsAGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.679_681delinsAGC MANE Select NP_478123.1:p.Pro227Ser
ENST00000337432.9:c.679_681delinsAGC MANE Select ENSP00000336701.4:p.Pro227Ser
NM_058216.2:c.679_681delinsAGC NP_478123.1:p.Pro227Ser
NR_103872.1:n.583_585delinsAGC
NR_103872.2:n.554_556delinsAGC
ENST00000337432.8:c.679_681delinsAGC ENSP00000336701.4:p.Pro227Ser
ENST00000413590.5:c.317_319delinsAGC
ENST00000425173.5:c.475_477delinsAGC ENSP00000407282.1:p.Pro159Ser
ENST00000461271.5:c.328_330delinsAGC ENSP00000464056.1:p.Pro110Ser
ENST00000461271.6:c.328_330delinsAGC ENSP00000464056.2:p.Pro110Ser
ENST00000475762.5:c.*1382_*1384delinsAGC ENSP00000432421.1:n.*1382_*1384delinsAGC
ENST00000482007.5:c.*107_*109delinsAGC ENSP00000433332.1:n.*107_*109delinsAGC
ENST00000487525.5:c.*107_*109delinsAGC ENSP00000431637.1:n.*107_*109delinsAGC
ENST00000487921.5:n.591_593delinsAGC
ENST00000583539.5:c.679_681delinsAGC ENSP00000463121.1:p.Pro227Ser
ENST00000584617.5:c.401_403delinsAGC
ENST00000697677.1:n.1760_1762delinsAGC
ENST00000697678.1:n.581_583delinsAGC
ENST00000697679.1:n.1753_1755delinsAGC
ENST00000697680.1:c.*1543_*1545delinsAGC ENSP00000513392.1:n.*1543_*1545delinsAGC
ENST00000697681.1:c.*1695_*1697delinsAGC ENSP00000513393.1:n.*1695_*1697delinsAGC
ENST00000697683.1:c.*1543_*1545delinsAGC ENSP00000513395.1:n.*1543_*1545delinsAGC
ENST00000697684.1:n.739_741delinsAGC
ENST00000697685.1:c.*1376_*1378delinsAGC ENSP00000513396.1:n.*1376_*1378delinsAGC
ENST00000697686.1:c.328_330delinsAGC ENSP00000513397.1:p.Pro110Ser
ENST00000697687.1:n.558_560delinsAGC
ENST00000697688.1:n.725_727delinsAGC
ENST00000697689.1:c.*1215_*1217delinsAGC ENSP00000513398.1:n.*1215_*1217delinsAGC
ENST00000697690.1:c.679_681delinsAGC ENSP00000513399.1:p.Pro227Ser
ENST00000697691.1:c.*651_*653delinsAGC ENSP00000513400.1:n.*651_*653delinsAGC
ENST00000697692.1:c.*691_*693delinsAGC ENSP00000513401.1:n.*691_*693delinsAGC
ENST00000697694.1:c.328_330delinsAGC ENSP00000513402.1:p.Pro110Ser
ENST00000697695.1:n.1286_1288delinsAGC
XM_006722001.2:c.679_681delinsAGC XP_006722064.1:p.Pro227Ser
XM_006722001.4:c.679_681delinsAGC XP_006722064.1:p.Pro227Ser
XM_006722002.2:c.679_681delinsAGC XP_006722065.1:p.Pro227Ser
XM_006722002.4:c.679_681delinsAGC XP_006722065.1:p.Pro227Ser
XM_006722004.2:c.328_330delinsAGC XP_006722067.1:p.Pro110Ser
XM_006722004.3:c.328_330delinsAGC XP_006722067.1:p.Pro110Ser
XM_006722005.2:c.328_330delinsAGC XP_006722068.1:p.Pro110Ser
XM_006722005.3:c.328_330delinsAGC XP_006722068.1:p.Pro110Ser
XM_011525092.1:c.328_330delinsAGC XP_011523394.1:p.Pro110Ser
XM_011525092.2:c.328_330delinsAGC XP_011523394.1:p.Pro110Ser
XM_011525093.1:c.328_330delinsAGC XP_011523395.1:p.Pro110Ser
XM_011525093.2:c.328_330delinsAGC XP_011523395.1:p.Pro110Ser
XM_011525094.1:c.328_330delinsAGC XP_011523396.1:p.Pro110Ser
XM_011525094.2:c.328_330delinsAGC XP_011523396.1:p.Pro110Ser
XM_017024914.1:c.328_330delinsAGC XP_016880403.1:p.Pro110Ser
XM_017024915.1:c.328_330delinsAGC XP_016880404.1:p.Pro110Ser
XM_017024916.1:c.328_330delinsAGC XP_016880405.1:p.Pro110Ser
XM_017024917.1:c.328_330delinsAGC XP_016880406.1:p.Pro110Ser
XM_017024918.2:c.328_330delinsAGC XP_016880407.1:p.Pro110Ser
XM_017024919.1:c.328_330delinsAGC XP_016880408.1:p.Pro110Ser
XR_934513.1:n.752_754delinsAGC
XR_934513.3:n.1183_1185delinsAGC
XR_934514.1:n.752_754delinsAGC
XR_934514.3:n.1183_1185delinsAGC