Canonical Allele Identifier: CA3261179520
Community Standard Title: NM_058216.3(RAD51C):c.1028_1029delinsTG (p.Pro343Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734119_58734120delinsTG , CM000679.2:g.58734119_58734120delinsTG GRCh38
NC_000017.10:g.56811480_56811481delinsTG , CM000679.1:g.56811480_56811481delinsTG GRCh37
NC_000017.9:g.54166479_54166480delinsTG NCBI36
NG_023199.1:g.46518_46519delinsTG , LRG_314:g.46518_46519delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1028_1029delinsTG MANE Select NP_478123.1:p.Pro343Leu
ENST00000337432.9:c.1028_1029delinsTG MANE Select ENSP00000336701.4:p.Pro343Leu
NM_058216.2:c.1028_1029delinsTG NP_478123.1:p.Pro343Leu
NR_103872.1:n.932_933delinsTG
NR_103872.2:n.903_904delinsTG
ENST00000337432.8:c.1028_1029delinsTG ENSP00000336701.4:p.Pro343Leu
ENST00000413590.5:c.669_670delinsTG
ENST00000461271.6:c.*1560_*1561delinsTG ENSP00000464056.2:n.*1560_*1561delinsTG
ENST00000461706.1:n.215_216delinsTG
ENST00000475762.5:c.*1664_*1665delinsTG ENSP00000432421.1:n.*1664_*1665delinsTG
ENST00000482007.5:c.*456_*457delinsTG ENSP00000433332.1:n.*456_*457delinsTG
ENST00000487525.5:c.*604_*605delinsTG ENSP00000431637.1:n.*604_*605delinsTG
ENST00000578151.1:n.241_242delinsTG
ENST00000581221.5:n.543_544delinsTG
ENST00000584804.1:c.262_263delinsTG ENSP00000463658.1:p.Leu88Cys
ENST00000697680.1:c.*1992_*1993delinsTG ENSP00000513392.1:n.*1992_*1993delinsTG
ENST00000697681.1:c.*2189_*2190delinsTG ENSP00000513393.1:n.*2189_*2190delinsTG
ENST00000697683.1:c.*1964_*1965delinsTG ENSP00000513395.1:n.*1964_*1965delinsTG
ENST00000697685.1:c.*1725_*1726delinsTG ENSP00000513396.1:n.*1725_*1726delinsTG
ENST00000697686.1:c.799_800delinsTG ENSP00000513397.1:p.Leu267Cys
ENST00000697689.1:c.*1442_*1443delinsTG ENSP00000513398.1:n.*1442_*1443delinsTG
ENST00000697690.1:c.906_907delinsTG ENSP00000513399.1:p.Ser303Ala
ENST00000697691.1:c.*1000_*1001delinsTG ENSP00000513400.1:n.*1000_*1001delinsTG
ENST00000697692.1:c.*1040_*1041delinsTG ENSP00000513401.1:n.*1040_*1041delinsTG
ENST00000697694.1:c.677_678delinsTG ENSP00000513402.1:p.Pro226Leu
ENST00000697695.1:n.1635_1636delinsTG
XM_006722001.2:c.1031_1032delinsTG XP_006722064.1:p.Pro344Leu
XM_006722001.4:c.1031_1032delinsTG XP_006722064.1:p.Pro344Leu
XM_006722002.2:c.967_968delinsTG XP_006722065.1:p.Leu323Cys
XM_006722002.4:c.967_968delinsTG XP_006722065.1:p.Leu323Cys
XM_006722004.2:c.680_681delinsTG XP_006722067.1:p.Pro227Leu
XM_006722004.3:c.680_681delinsTG XP_006722067.1:p.Pro227Leu
XM_006722005.2:c.680_681delinsTG XP_006722068.1:p.Pro227Leu
XM_006722005.3:c.680_681delinsTG XP_006722068.1:p.Pro227Leu
XM_011525092.1:c.680_681delinsTG XP_011523394.1:p.Pro227Leu
XM_011525092.2:c.680_681delinsTG XP_011523394.1:p.Pro227Leu
XM_011525093.1:c.680_681delinsTG XP_011523395.1:p.Pro227Leu
XM_011525093.2:c.680_681delinsTG XP_011523395.1:p.Pro227Leu
XM_011525094.1:c.680_681delinsTG XP_011523396.1:p.Pro227Leu
XM_011525094.2:c.680_681delinsTG XP_011523396.1:p.Pro227Leu
XM_017024914.1:c.677_678delinsTG XP_016880403.1:p.Pro226Leu
XM_017024915.1:c.677_678delinsTG XP_016880404.1:p.Pro226Leu
XM_017024916.1:c.677_678delinsTG XP_016880405.1:p.Pro226Leu
XM_017024917.1:c.677_678delinsTG XP_016880406.1:p.Pro226Leu
XM_017024918.2:c.677_678delinsTG XP_016880407.1:p.Pro226Leu
XM_017024919.1:c.616_617delinsTG XP_016880408.1:p.Leu206Cys
XR_934513.1:n.1246_1247delinsTG
XR_934513.3:n.1677_1678delinsTG
XR_934514.1:n.1249_1250delinsTG
XR_934514.3:n.1680_1681delinsTG
XR_934886.1:n.149+3951_149+3952delinsCA
XR_934886.2:n.149+3951_149+3952delinsCA