Canonical Allele Identifier: CA3261179480
Community Standard Title: NM_058216.3(RAD51C):c.341_342delinsTG (p.Gly114Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695126_58695127delinsTG , CM000679.2:g.58695126_58695127delinsTG GRCh38
NC_000017.10:g.56772487_56772488delinsTG , CM000679.1:g.56772487_56772488delinsTG GRCh37
NC_000017.9:g.54127486_54127487delinsTG NCBI36
NG_023199.1:g.7525_7526delinsTG , LRG_314:g.7525_7526delinsTG
NG_047169.1:g.1953_1954delinsCA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.341_342delinsTG MANE Select NP_478123.1:p.Gly114Val
ENST00000337432.9:c.341_342delinsTG MANE Select ENSP00000336701.4:p.Gly114Val
NM_002876.3:c.341_342delinsTG NP_002867.1:p.Gly114Val
NM_002876.4:c.341_342delinsTG NP_002867.1:p.Gly114Val
NM_058216.2:c.341_342delinsTG NP_478123.1:p.Gly114Val
NR_103872.1:n.412_413delinsTG
NR_103872.2:n.383_384delinsTG
NR_103873.1:n.309_310delinsTG
ENST00000337432.8:c.341_342delinsTG ENSP00000336701.4:p.Gly114Val
ENST00000421782.3:c.341_342delinsTG ENSP00000391450.2:p.Gly114Val
ENST00000425173.5:c.137_138delinsTG ENSP00000407282.1:p.Gly46Val
ENST00000461271.5:c.-11_-10delinsTG ENSP00000464056.1:n.-11_-10delinsTG
ENST00000461271.6:c.-11_-10delinsTG ENSP00000464056.2:n.-11_-10delinsTG
ENST00000475762.5:c.*1044_*1045delinsTG ENSP00000432421.1:n.*1044_*1045delinsTG
ENST00000482007.5:c.341_342delinsTG ENSP00000433332.1:p.Gly114Val
ENST00000486827.1:c.*1205_*1206delinsTG ENSP00000436761.1:n.*1205_*1206delinsTG
ENST00000487525.5:c.341_342delinsTG ENSP00000431637.1:p.Gly114Val
ENST00000487921.5:n.253_254delinsTG
ENST00000583539.5:c.341_342delinsTG ENSP00000463121.1:p.Gly114Val
ENST00000584617.5:c.127-1567_127-1566delinsTG
ENST00000622327.4:c.77_78delinsTG ENSP00000482326.1:p.Gly26Val
ENST00000697675.1:n.1435_1436delinsTG
ENST00000697676.1:n.401_402delinsTG
ENST00000697677.1:n.1422_1423delinsTG
ENST00000697678.1:n.243_244delinsTG
ENST00000697679.1:n.1415_1416delinsTG
ENST00000697680.1:c.*1205_*1206delinsTG ENSP00000513392.1:n.*1205_*1206delinsTG
ENST00000697681.1:c.*1205_*1206delinsTG ENSP00000513393.1:n.*1205_*1206delinsTG
ENST00000697683.1:c.*1205_*1206delinsTG ENSP00000513395.1:n.*1205_*1206delinsTG
ENST00000697684.1:n.401_402delinsTG
ENST00000697685.1:c.*1205_*1206delinsTG ENSP00000513396.1:n.*1205_*1206delinsTG
ENST00000697686.1:c.-11_-10delinsTG ENSP00000513397.1:n.-11_-10delinsTG
ENST00000697687.1:n.387_388delinsTG
ENST00000697688.1:n.387_388delinsTG
ENST00000697689.1:c.*1044_*1045delinsTG ENSP00000513398.1:n.*1044_*1045delinsTG
ENST00000697690.1:c.341_342delinsTG ENSP00000513399.1:p.Gly114Val
ENST00000697691.1:c.*313_*314delinsTG ENSP00000513400.1:n.*313_*314delinsTG
ENST00000697692.1:c.*353_*354delinsTG ENSP00000513401.1:n.*353_*354delinsTG
ENST00000697693.1:n.1116_1117delinsTG
ENST00000697694.1:c.-11_-10delinsTG ENSP00000513402.1:n.-11_-10delinsTG
ENST00000697695.1:n.948_949delinsTG
XM_006722001.2:c.341_342delinsTG XP_006722064.1:p.Gly114Val
XM_006722001.4:c.341_342delinsTG XP_006722064.1:p.Gly114Val
XM_006722002.2:c.341_342delinsTG XP_006722065.1:p.Gly114Val
XM_006722002.4:c.341_342delinsTG XP_006722065.1:p.Gly114Val
XM_006722004.2:c.-11_-10delinsTG XP_006722067.1:n.-11_-10delinsTG
XM_006722004.3:c.-11_-10delinsTG XP_006722067.1:n.-11_-10delinsTG
XM_006722005.2:c.-11_-10delinsTG XP_006722068.1:n.-11_-10delinsTG
XM_006722005.3:c.-11_-10delinsTG XP_006722068.1:n.-11_-10delinsTG
XM_011525092.1:c.-11_-10delinsTG XP_011523394.1:n.-11_-10delinsTG
XM_011525092.2:c.-11_-10delinsTG XP_011523394.1:n.-11_-10delinsTG
XM_011525093.1:c.-11_-10delinsTG XP_011523395.1:n.-11_-10delinsTG
XM_011525093.2:c.-11_-10delinsTG XP_011523395.1:n.-11_-10delinsTG
XM_011525094.1:c.-11_-10delinsTG XP_011523396.1:n.-11_-10delinsTG
XM_011525094.2:c.-11_-10delinsTG XP_011523396.1:n.-11_-10delinsTG
XM_017024914.1:c.-11_-10delinsTG XP_016880403.1:n.-11_-10delinsTG
XM_017024915.1:c.-11_-10delinsTG XP_016880404.1:n.-11_-10delinsTG
XM_017024916.1:c.-11_-10delinsTG XP_016880405.1:n.-11_-10delinsTG
XM_017024917.1:c.-11_-10delinsTG XP_016880406.1:n.-11_-10delinsTG
XM_017024918.2:c.-11_-10delinsTG XP_016880407.1:n.-11_-10delinsTG
XM_017024919.1:c.-11_-10delinsTG XP_016880408.1:n.-11_-10delinsTG
XR_934513.1:n.414_415delinsTG
XR_934513.3:n.845_846delinsTG
XR_934514.1:n.414_415delinsTG
XR_934514.3:n.845_846delinsTG