Canonical Allele Identifier: CA3057243529
Community Standard Title: NM_058216.3(RAD51C):c.1072_1073delinsAG (p.Gln358Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734163_58734164delinsAG , CM000679.2:g.58734163_58734164delinsAG GRCh38
NC_000017.10:g.56811524_56811525delinsAG , CM000679.1:g.56811524_56811525delinsAG GRCh37
NC_000017.9:g.54166523_54166524delinsAG NCBI36
NG_023199.1:g.46562_46563delinsAG , LRG_314:g.46562_46563delinsAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1072_1073delinsAG MANE Select NP_478123.1:p.Gln358Arg
ENST00000337432.9:c.1072_1073delinsAG MANE Select ENSP00000336701.4:p.Gln358Arg
NM_058216.2:c.1072_1073delinsAG NP_478123.1:p.Gln358Arg
NR_103872.1:n.976_977delinsAG
NR_103872.2:n.947_948delinsAG
ENST00000337432.8:c.1072_1073delinsAG ENSP00000336701.4:p.Gln358Arg
ENST00000413590.5:c.713_714delinsAG
ENST00000461271.6:c.*1604_*1605delinsAG ENSP00000464056.2:n.*1604_*1605delinsAG
ENST00000461706.1:n.259_260delinsAG
ENST00000475762.5:c.*1708_*1709delinsAG ENSP00000432421.1:n.*1708_*1709delinsAG
ENST00000482007.5:c.*500_*501delinsAG ENSP00000433332.1:n.*500_*501delinsAG
ENST00000487525.5:c.*648_*649delinsAG ENSP00000431637.1:n.*648_*649delinsAG
ENST00000578151.1:n.285_286delinsAG
ENST00000581221.5:n.587_588delinsAG
ENST00000584804.1:c.306_307delinsAG ENSP00000463658.1:p.Cys102Ter
ENST00000697680.1:c.*2036_*2037delinsAG ENSP00000513392.1:n.*2036_*2037delinsAG
ENST00000697681.1:c.*2233_*2234delinsAG ENSP00000513393.1:n.*2233_*2234delinsAG
ENST00000697683.1:c.*2008_*2009delinsAG ENSP00000513395.1:n.*2008_*2009delinsAG
ENST00000697685.1:c.*1769_*1770delinsAG ENSP00000513396.1:n.*1769_*1770delinsAG
ENST00000697686.1:c.843_844delinsAG ENSP00000513397.1:p.Cys281Ter
ENST00000697689.1:c.*1486_*1487delinsAG ENSP00000513398.1:n.*1486_*1487delinsAG
ENST00000697690.1:c.*32_*33delinsAG ENSP00000513399.1:n.*32_*33delinsAG
ENST00000697691.1:c.*1044_*1045delinsAG ENSP00000513400.1:n.*1044_*1045delinsAG
ENST00000697692.1:c.*1084_*1085delinsAG ENSP00000513401.1:n.*1084_*1085delinsAG
ENST00000697694.1:c.721_722delinsAG ENSP00000513402.1:p.Gln241Arg
ENST00000697695.1:n.1679_1680delinsAG
XM_006722001.2:c.1075_1076delinsAG XP_006722064.1:p.Gln359Arg
XM_006722001.4:c.1075_1076delinsAG XP_006722064.1:p.Gln359Arg
XM_006722002.2:c.1011_1012delinsAG XP_006722065.1:p.Cys337Ter
XM_006722002.4:c.1011_1012delinsAG XP_006722065.1:p.Cys337Ter
XM_006722004.2:c.724_725delinsAG XP_006722067.1:p.Gln242Arg
XM_006722004.3:c.724_725delinsAG XP_006722067.1:p.Gln242Arg
XM_006722005.2:c.724_725delinsAG XP_006722068.1:p.Gln242Arg
XM_006722005.3:c.724_725delinsAG XP_006722068.1:p.Gln242Arg
XM_011525092.1:c.724_725delinsAG XP_011523394.1:p.Gln242Arg
XM_011525092.2:c.724_725delinsAG XP_011523394.1:p.Gln242Arg
XM_011525093.1:c.724_725delinsAG XP_011523395.1:p.Gln242Arg
XM_011525093.2:c.724_725delinsAG XP_011523395.1:p.Gln242Arg
XM_011525094.1:c.724_725delinsAG XP_011523396.1:p.Gln242Arg
XM_011525094.2:c.724_725delinsAG XP_011523396.1:p.Gln242Arg
XM_017024914.1:c.721_722delinsAG XP_016880403.1:p.Gln241Arg
XM_017024915.1:c.721_722delinsAG XP_016880404.1:p.Gln241Arg
XM_017024916.1:c.721_722delinsAG XP_016880405.1:p.Gln241Arg
XM_017024917.1:c.721_722delinsAG XP_016880406.1:p.Gln241Arg
XM_017024918.2:c.721_722delinsAG XP_016880407.1:p.Gln241Arg
XM_017024919.1:c.660_661delinsAG XP_016880408.1:p.Cys220Ter
XR_934513.1:n.1290_1291delinsAG
XR_934513.3:n.1721_1722delinsAG
XR_934514.1:n.1293_1294delinsAG
XR_934514.3:n.1724_1725delinsAG
XR_934886.1:n.149+3907_149+3908delinsCT
XR_934886.2:n.149+3907_149+3908delinsCT