Canonical Allele Identifier: CA3261180196
Community Standard Title: NM_058216.3(RAD51C):c.1061_1062delinsTG (p.Ala354Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734152_58734153delinsTG , CM000679.2:g.58734152_58734153delinsTG GRCh38
NC_000017.10:g.56811513_56811514delinsTG , CM000679.1:g.56811513_56811514delinsTG GRCh37
NC_000017.9:g.54166512_54166513delinsTG NCBI36
NG_023199.1:g.46551_46552delinsTG , LRG_314:g.46551_46552delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1061_1062delinsTG MANE Select NP_478123.1:p.Ala354Val
ENST00000337432.9:c.1061_1062delinsTG MANE Select ENSP00000336701.4:p.Ala354Val
NM_058216.2:c.1061_1062delinsTG NP_478123.1:p.Ala354Val
NR_103872.1:n.965_966delinsTG
NR_103872.2:n.936_937delinsTG
ENST00000337432.8:c.1061_1062delinsTG ENSP00000336701.4:p.Ala354Val
ENST00000413590.5:c.702_703delinsTG
ENST00000461271.6:c.*1593_*1594delinsTG ENSP00000464056.2:n.*1593_*1594delinsTG
ENST00000461706.1:n.248_249delinsTG
ENST00000475762.5:c.*1697_*1698delinsTG ENSP00000432421.1:n.*1697_*1698delinsTG
ENST00000482007.5:c.*489_*490delinsTG ENSP00000433332.1:n.*489_*490delinsTG
ENST00000487525.5:c.*637_*638delinsTG ENSP00000431637.1:n.*637_*638delinsTG
ENST00000578151.1:n.274_275delinsTG
ENST00000581221.5:n.576_577delinsTG
ENST00000584804.1:c.295_296delinsTG ENSP00000463658.1:p.His99Cys
ENST00000697680.1:c.*2025_*2026delinsTG ENSP00000513392.1:n.*2025_*2026delinsTG
ENST00000697681.1:c.*2222_*2223delinsTG ENSP00000513393.1:n.*2222_*2223delinsTG
ENST00000697683.1:c.*1997_*1998delinsTG ENSP00000513395.1:n.*1997_*1998delinsTG
ENST00000697685.1:c.*1758_*1759delinsTG ENSP00000513396.1:n.*1758_*1759delinsTG
ENST00000697686.1:c.832_833delinsTG ENSP00000513397.1:p.His278Cys
ENST00000697689.1:c.*1475_*1476delinsTG ENSP00000513398.1:n.*1475_*1476delinsTG
ENST00000697690.1:c.*21_*22delinsTG ENSP00000513399.1:n.*21_*22delinsTG
ENST00000697691.1:c.*1033_*1034delinsTG ENSP00000513400.1:n.*1033_*1034delinsTG
ENST00000697692.1:c.*1073_*1074delinsTG ENSP00000513401.1:n.*1073_*1074delinsTG
ENST00000697694.1:c.710_711delinsTG ENSP00000513402.1:p.Ala237Val
ENST00000697695.1:n.1668_1669delinsTG
XM_006722001.2:c.1064_1065delinsTG XP_006722064.1:p.Ala355Val
XM_006722001.4:c.1064_1065delinsTG XP_006722064.1:p.Ala355Val
XM_006722002.2:c.1000_1001delinsTG XP_006722065.1:p.His334Cys
XM_006722002.4:c.1000_1001delinsTG XP_006722065.1:p.His334Cys
XM_006722004.2:c.713_714delinsTG XP_006722067.1:p.Ala238Val
XM_006722004.3:c.713_714delinsTG XP_006722067.1:p.Ala238Val
XM_006722005.2:c.713_714delinsTG XP_006722068.1:p.Ala238Val
XM_006722005.3:c.713_714delinsTG XP_006722068.1:p.Ala238Val
XM_011525092.1:c.713_714delinsTG XP_011523394.1:p.Ala238Val
XM_011525092.2:c.713_714delinsTG XP_011523394.1:p.Ala238Val
XM_011525093.1:c.713_714delinsTG XP_011523395.1:p.Ala238Val
XM_011525093.2:c.713_714delinsTG XP_011523395.1:p.Ala238Val
XM_011525094.1:c.713_714delinsTG XP_011523396.1:p.Ala238Val
XM_011525094.2:c.713_714delinsTG XP_011523396.1:p.Ala238Val
XM_017024914.1:c.710_711delinsTG XP_016880403.1:p.Ala237Val
XM_017024915.1:c.710_711delinsTG XP_016880404.1:p.Ala237Val
XM_017024916.1:c.710_711delinsTG XP_016880405.1:p.Ala237Val
XM_017024917.1:c.710_711delinsTG XP_016880406.1:p.Ala237Val
XM_017024918.2:c.710_711delinsTG XP_016880407.1:p.Ala237Val
XM_017024919.1:c.649_650delinsTG XP_016880408.1:p.His217Cys
XR_934513.1:n.1279_1280delinsTG
XR_934513.3:n.1710_1711delinsTG
XR_934514.1:n.1282_1283delinsTG
XR_934514.3:n.1713_1714delinsTG
XR_934886.1:n.149+3918_149+3919delinsCA
XR_934886.2:n.149+3918_149+3919delinsCA