Canonical Allele Identifier: CA3057242699
Community Standard Title: NM_058216.3(RAD51C):c.702_703delinsTG (p.Lys235Glu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703326_58703327delinsTG , CM000679.2:g.58703326_58703327delinsTG GRCh38
NC_000017.10:g.56780687_56780688delinsTG , CM000679.1:g.56780687_56780688delinsTG GRCh37
NC_000017.9:g.54135686_54135687delinsTG NCBI36
NG_023199.1:g.15725_15726delinsTG , LRG_314:g.15725_15726delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.702_703delinsTG MANE Select NP_478123.1:p.Lys235Glu
ENST00000337432.9:c.702_703delinsTG MANE Select ENSP00000336701.4:p.Lys235Glu
NM_058216.2:c.702_703delinsTG NP_478123.1:p.Lys235Glu
NR_103872.1:n.606_607delinsTG
NR_103872.2:n.577_578delinsTG
ENST00000337432.8:c.702_703delinsTG ENSP00000336701.4:p.Lys235Glu
ENST00000413590.5:c.340_341delinsTG
ENST00000425173.5:c.498_499delinsTG ENSP00000407282.1:p.Lys167Glu
ENST00000461271.5:c.351_352delinsTG ENSP00000464056.1:p.Lys118Glu
ENST00000461271.6:c.351_352delinsTG ENSP00000464056.2:p.Lys118Glu
ENST00000475762.5:c.*1405_*1406delinsTG ENSP00000432421.1:n.*1405_*1406delinsTG
ENST00000482007.5:c.*130_*131delinsTG ENSP00000433332.1:n.*130_*131delinsTG
ENST00000487525.5:c.*130_*131delinsTG ENSP00000431637.1:n.*130_*131delinsTG
ENST00000487921.5:n.614_615delinsTG
ENST00000583539.5:c.702_703delinsTG ENSP00000463121.1:p.Lys235Glu
ENST00000584617.5:c.424_425delinsTG
ENST00000697677.1:n.1783_1784delinsTG
ENST00000697678.1:n.604_605delinsTG
ENST00000697679.1:n.1776_1777delinsTG
ENST00000697680.1:c.*1566_*1567delinsTG ENSP00000513392.1:n.*1566_*1567delinsTG
ENST00000697681.1:c.*1718_*1719delinsTG ENSP00000513393.1:n.*1718_*1719delinsTG
ENST00000697683.1:c.*1566_*1567delinsTG ENSP00000513395.1:n.*1566_*1567delinsTG
ENST00000697684.1:n.762_763delinsTG
ENST00000697685.1:c.*1399_*1400delinsTG ENSP00000513396.1:n.*1399_*1400delinsTG
ENST00000697686.1:c.351_352delinsTG ENSP00000513397.1:p.Lys118Glu
ENST00000697687.1:n.581_582delinsTG
ENST00000697688.1:n.748_749delinsTG
ENST00000697689.1:c.*1238_*1239delinsTG ENSP00000513398.1:n.*1238_*1239delinsTG
ENST00000697690.1:c.702_703delinsTG ENSP00000513399.1:p.Lys235Glu
ENST00000697691.1:c.*674_*675delinsTG ENSP00000513400.1:n.*674_*675delinsTG
ENST00000697692.1:c.*714_*715delinsTG ENSP00000513401.1:n.*714_*715delinsTG
ENST00000697694.1:c.351_352delinsTG ENSP00000513402.1:p.Lys118Glu
ENST00000697695.1:n.1309_1310delinsTG
XM_006722001.2:c.702_703delinsTG XP_006722064.1:p.Lys235Glu
XM_006722001.4:c.702_703delinsTG XP_006722064.1:p.Lys235Glu
XM_006722002.2:c.702_703delinsTG XP_006722065.1:p.Lys235Glu
XM_006722002.4:c.702_703delinsTG XP_006722065.1:p.Lys235Glu
XM_006722004.2:c.351_352delinsTG XP_006722067.1:p.Lys118Glu
XM_006722004.3:c.351_352delinsTG XP_006722067.1:p.Lys118Glu
XM_006722005.2:c.351_352delinsTG XP_006722068.1:p.Lys118Glu
XM_006722005.3:c.351_352delinsTG XP_006722068.1:p.Lys118Glu
XM_011525092.1:c.351_352delinsTG XP_011523394.1:p.Lys118Glu
XM_011525092.2:c.351_352delinsTG XP_011523394.1:p.Lys118Glu
XM_011525093.1:c.351_352delinsTG XP_011523395.1:p.Lys118Glu
XM_011525093.2:c.351_352delinsTG XP_011523395.1:p.Lys118Glu
XM_011525094.1:c.351_352delinsTG XP_011523396.1:p.Lys118Glu
XM_011525094.2:c.351_352delinsTG XP_011523396.1:p.Lys118Glu
XM_017024914.1:c.351_352delinsTG XP_016880403.1:p.Lys118Glu
XM_017024915.1:c.351_352delinsTG XP_016880404.1:p.Lys118Glu
XM_017024916.1:c.351_352delinsTG XP_016880405.1:p.Lys118Glu
XM_017024917.1:c.351_352delinsTG XP_016880406.1:p.Lys118Glu
XM_017024918.2:c.351_352delinsTG XP_016880407.1:p.Lys118Glu
XM_017024919.1:c.351_352delinsTG XP_016880408.1:p.Lys118Glu
XR_934513.1:n.775_776delinsTG
XR_934513.3:n.1206_1207delinsTG
XR_934514.1:n.775_776delinsTG
XR_934514.3:n.1206_1207delinsTG