Canonical Allele Identifier: CA3057243530
Community Standard Title: NM_058216.3(RAD51C):c.1072_1073delinsTG (p.Gln358Ter)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734163_58734164delinsTG , CM000679.2:g.58734163_58734164delinsTG GRCh38
NC_000017.10:g.56811524_56811525delinsTG , CM000679.1:g.56811524_56811525delinsTG GRCh37
NC_000017.9:g.54166523_54166524delinsTG NCBI36
NG_023199.1:g.46562_46563delinsTG , LRG_314:g.46562_46563delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1072_1073delinsTG MANE Select NP_478123.1:p.Gln358Ter
ENST00000337432.9:c.1072_1073delinsTG MANE Select ENSP00000336701.4:p.Gln358Ter
NM_058216.2:c.1072_1073delinsTG NP_478123.1:p.Gln358Ter
NR_103872.1:n.976_977delinsTG
NR_103872.2:n.947_948delinsTG
ENST00000337432.8:c.1072_1073delinsTG ENSP00000336701.4:p.Gln358Ter
ENST00000413590.5:c.713_714delinsTG
ENST00000461271.6:c.*1604_*1605delinsTG ENSP00000464056.2:n.*1604_*1605delinsTG
ENST00000461706.1:n.259_260delinsTG
ENST00000475762.5:c.*1708_*1709delinsTG ENSP00000432421.1:n.*1708_*1709delinsTG
ENST00000482007.5:c.*500_*501delinsTG ENSP00000433332.1:n.*500_*501delinsTG
ENST00000487525.5:c.*648_*649delinsTG ENSP00000431637.1:n.*648_*649delinsTG
ENST00000578151.1:n.285_286delinsTG
ENST00000581221.5:n.587_588delinsTG
ENST00000584804.1:c.306_307delinsTG ENSP00000463658.1:p.Lys103Glu
ENST00000697680.1:c.*2036_*2037delinsTG ENSP00000513392.1:n.*2036_*2037delinsTG
ENST00000697681.1:c.*2233_*2234delinsTG ENSP00000513393.1:n.*2233_*2234delinsTG
ENST00000697683.1:c.*2008_*2009delinsTG ENSP00000513395.1:n.*2008_*2009delinsTG
ENST00000697685.1:c.*1769_*1770delinsTG ENSP00000513396.1:n.*1769_*1770delinsTG
ENST00000697686.1:c.843_844delinsTG ENSP00000513397.1:p.Lys282Glu
ENST00000697689.1:c.*1486_*1487delinsTG ENSP00000513398.1:n.*1486_*1487delinsTG
ENST00000697690.1:c.*32_*33delinsTG ENSP00000513399.1:n.*32_*33delinsTG
ENST00000697691.1:c.*1044_*1045delinsTG ENSP00000513400.1:n.*1044_*1045delinsTG
ENST00000697692.1:c.*1084_*1085delinsTG ENSP00000513401.1:n.*1084_*1085delinsTG
ENST00000697694.1:c.721_722delinsTG ENSP00000513402.1:p.Gln241Ter
ENST00000697695.1:n.1679_1680delinsTG
XM_006722001.2:c.1075_1076delinsTG XP_006722064.1:p.Gln359Ter
XM_006722001.4:c.1075_1076delinsTG XP_006722064.1:p.Gln359Ter
XM_006722002.2:c.1011_1012delinsTG XP_006722065.1:p.Lys338Glu
XM_006722002.4:c.1011_1012delinsTG XP_006722065.1:p.Lys338Glu
XM_006722004.2:c.724_725delinsTG XP_006722067.1:p.Gln242Ter
XM_006722004.3:c.724_725delinsTG XP_006722067.1:p.Gln242Ter
XM_006722005.2:c.724_725delinsTG XP_006722068.1:p.Gln242Ter
XM_006722005.3:c.724_725delinsTG XP_006722068.1:p.Gln242Ter
XM_011525092.1:c.724_725delinsTG XP_011523394.1:p.Gln242Ter
XM_011525092.2:c.724_725delinsTG XP_011523394.1:p.Gln242Ter
XM_011525093.1:c.724_725delinsTG XP_011523395.1:p.Gln242Ter
XM_011525093.2:c.724_725delinsTG XP_011523395.1:p.Gln242Ter
XM_011525094.1:c.724_725delinsTG XP_011523396.1:p.Gln242Ter
XM_011525094.2:c.724_725delinsTG XP_011523396.1:p.Gln242Ter
XM_017024914.1:c.721_722delinsTG XP_016880403.1:p.Gln241Ter
XM_017024915.1:c.721_722delinsTG XP_016880404.1:p.Gln241Ter
XM_017024916.1:c.721_722delinsTG XP_016880405.1:p.Gln241Ter
XM_017024917.1:c.721_722delinsTG XP_016880406.1:p.Gln241Ter
XM_017024918.2:c.721_722delinsTG XP_016880407.1:p.Gln241Ter
XM_017024919.1:c.660_661delinsTG XP_016880408.1:p.Lys221Glu
XR_934513.1:n.1290_1291delinsTG
XR_934513.3:n.1721_1722delinsTG
XR_934514.1:n.1293_1294delinsTG
XR_934514.3:n.1724_1725delinsTG
XR_934886.1:n.149+3907_149+3908delinsCA
XR_934886.2:n.149+3907_149+3908delinsCA