Canonical Allele Identifier: CA3261180340
Community Standard Title: NM_058216.3(RAD51C):c.1072_1074delinsGAG (p.Gln358Glu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734163_58734165delinsGAG , CM000679.2:g.58734163_58734165delinsGAG GRCh38
NC_000017.10:g.56811524_56811526delinsGAG , CM000679.1:g.56811524_56811526delinsGAG GRCh37
NC_000017.9:g.54166523_54166525delinsGAG NCBI36
NG_023199.1:g.46562_46564delinsGAG , LRG_314:g.46562_46564delinsGAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1072_1074delinsGAG MANE Select NP_478123.1:p.Gln358Glu
ENST00000337432.9:c.1072_1074delinsGAG MANE Select ENSP00000336701.4:p.Gln358Glu
NM_058216.2:c.1072_1074delinsGAG NP_478123.1:p.Gln358Glu
NR_103872.1:n.976_978delinsGAG
NR_103872.2:n.947_949delinsGAG
ENST00000337432.8:c.1072_1074delinsGAG ENSP00000336701.4:p.Gln358Glu
ENST00000413590.5:c.713_715delinsGAG
ENST00000461271.6:c.*1604_*1606delinsGAG ENSP00000464056.2:n.*1604_*1606delinsGAG
ENST00000461706.1:n.259_261delinsGAG
ENST00000475762.5:c.*1708_*1710delinsGAG ENSP00000432421.1:n.*1708_*1710delinsGAG
ENST00000482007.5:c.*500_*502delinsGAG ENSP00000433332.1:n.*500_*502delinsGAG
ENST00000487525.5:c.*648_*650delinsGAG ENSP00000431637.1:n.*648_*650delinsGAG
ENST00000578151.1:n.285_287delinsGAG
ENST00000581221.5:n.587_589delinsGAG
ENST00000584804.1:c.306_308delinsGAG ENSP00000463658.1:p.Cys102_Lys103delinsTrpArg
ENST00000697680.1:c.*2036_*2038delinsGAG ENSP00000513392.1:n.*2036_*2038delinsGAG
ENST00000697681.1:c.*2233_*2235delinsGAG ENSP00000513393.1:n.*2233_*2235delinsGAG
ENST00000697683.1:c.*2008_*2010delinsGAG ENSP00000513395.1:n.*2008_*2010delinsGAG
ENST00000697685.1:c.*1769_*1771delinsGAG ENSP00000513396.1:n.*1769_*1771delinsGAG
ENST00000697686.1:c.843_845delinsGAG ENSP00000513397.1:p.Cys281_Lys282delinsTrpArg
ENST00000697689.1:c.*1486_*1488delinsGAG ENSP00000513398.1:n.*1486_*1488delinsGAG
ENST00000697690.1:c.*32_*34delinsGAG ENSP00000513399.1:n.*32_*34delinsGAG
ENST00000697691.1:c.*1044_*1046delinsGAG ENSP00000513400.1:n.*1044_*1046delinsGAG
ENST00000697692.1:c.*1084_*1086delinsGAG ENSP00000513401.1:n.*1084_*1086delinsGAG
ENST00000697694.1:c.721_723delinsGAG ENSP00000513402.1:p.Gln241Glu
ENST00000697695.1:n.1679_1681delinsGAG
XM_006722001.2:c.1075_1077delinsGAG XP_006722064.1:p.Gln359Glu
XM_006722001.4:c.1075_1077delinsGAG XP_006722064.1:p.Gln359Glu
XM_006722002.2:c.1011_1013delinsGAG XP_006722065.1:p.Cys337_Lys338delinsTrpArg
XM_006722002.4:c.1011_1013delinsGAG XP_006722065.1:p.Cys337_Lys338delinsTrpArg
XM_006722004.2:c.724_726delinsGAG XP_006722067.1:p.Gln242Glu
XM_006722004.3:c.724_726delinsGAG XP_006722067.1:p.Gln242Glu
XM_006722005.2:c.724_726delinsGAG XP_006722068.1:p.Gln242Glu
XM_006722005.3:c.724_726delinsGAG XP_006722068.1:p.Gln242Glu
XM_011525092.1:c.724_726delinsGAG XP_011523394.1:p.Gln242Glu
XM_011525092.2:c.724_726delinsGAG XP_011523394.1:p.Gln242Glu
XM_011525093.1:c.724_726delinsGAG XP_011523395.1:p.Gln242Glu
XM_011525093.2:c.724_726delinsGAG XP_011523395.1:p.Gln242Glu
XM_011525094.1:c.724_726delinsGAG XP_011523396.1:p.Gln242Glu
XM_011525094.2:c.724_726delinsGAG XP_011523396.1:p.Gln242Glu
XM_017024914.1:c.721_723delinsGAG XP_016880403.1:p.Gln241Glu
XM_017024915.1:c.721_723delinsGAG XP_016880404.1:p.Gln241Glu
XM_017024916.1:c.721_723delinsGAG XP_016880405.1:p.Gln241Glu
XM_017024917.1:c.721_723delinsGAG XP_016880406.1:p.Gln241Glu
XM_017024918.2:c.721_723delinsGAG XP_016880407.1:p.Gln241Glu
XM_017024919.1:c.660_662delinsGAG XP_016880408.1:p.Cys220_Lys221delinsTrpArg
XR_934513.1:n.1290_1292delinsGAG
XR_934513.3:n.1721_1723delinsGAG
XR_934514.1:n.1293_1295delinsGAG
XR_934514.3:n.1724_1726delinsGAG
XR_934886.1:n.149+3906_149+3908delinsCTC
XR_934886.2:n.149+3906_149+3908delinsCTC