Canonical Allele Identifier: CA3261179060
Community Standard Title: NM_058216.3(RAD51C):c.317_318delinsTG (p.Ala106Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695102_58695103delinsTG , CM000679.2:g.58695102_58695103delinsTG GRCh38
NC_000017.10:g.56772463_56772464delinsTG , CM000679.1:g.56772463_56772464delinsTG GRCh37
NC_000017.9:g.54127462_54127463delinsTG NCBI36
NG_023199.1:g.7501_7502delinsTG , LRG_314:g.7501_7502delinsTG
NG_047169.1:g.1977_1978delinsCA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.317_318delinsTG MANE Select NP_478123.1:p.Ala106Val
ENST00000337432.9:c.317_318delinsTG MANE Select ENSP00000336701.4:p.Ala106Val
NM_002876.3:c.317_318delinsTG NP_002867.1:p.Ala106Val
NM_002876.4:c.317_318delinsTG NP_002867.1:p.Ala106Val
NM_058216.2:c.317_318delinsTG NP_478123.1:p.Ala106Val
NR_103872.1:n.388_389delinsTG
NR_103872.2:n.359_360delinsTG
NR_103873.1:n.285_286delinsTG
ENST00000337432.8:c.317_318delinsTG ENSP00000336701.4:p.Ala106Val
ENST00000421782.3:c.317_318delinsTG ENSP00000391450.2:p.Ala106Val
ENST00000425173.5:c.113_114delinsTG ENSP00000407282.1:p.Ala38Val
ENST00000461271.5:c.-35_-34delinsTG ENSP00000464056.1:n.-35_-34delinsTG
ENST00000461271.6:c.-35_-34delinsTG ENSP00000464056.2:n.-35_-34delinsTG
ENST00000475762.5:c.*1020_*1021delinsTG ENSP00000432421.1:n.*1020_*1021delinsTG
ENST00000482007.5:c.317_318delinsTG ENSP00000433332.1:p.Ala106Val
ENST00000486827.1:c.*1181_*1182delinsTG ENSP00000436761.1:n.*1181_*1182delinsTG
ENST00000487525.5:c.317_318delinsTG ENSP00000431637.1:p.Ala106Val
ENST00000487921.5:n.229_230delinsTG
ENST00000583539.5:c.317_318delinsTG ENSP00000463121.1:p.Ala106Val
ENST00000584617.5:c.127-1591_127-1590delinsTG
ENST00000622327.4:c.53_54delinsTG ENSP00000482326.1:p.Ala18Val
ENST00000697675.1:n.1411_1412delinsTG
ENST00000697676.1:n.377_378delinsTG
ENST00000697677.1:n.1398_1399delinsTG
ENST00000697678.1:n.219_220delinsTG
ENST00000697679.1:n.1391_1392delinsTG
ENST00000697680.1:c.*1181_*1182delinsTG ENSP00000513392.1:n.*1181_*1182delinsTG
ENST00000697681.1:c.*1181_*1182delinsTG ENSP00000513393.1:n.*1181_*1182delinsTG
ENST00000697683.1:c.*1181_*1182delinsTG ENSP00000513395.1:n.*1181_*1182delinsTG
ENST00000697684.1:n.377_378delinsTG
ENST00000697685.1:c.*1181_*1182delinsTG ENSP00000513396.1:n.*1181_*1182delinsTG
ENST00000697686.1:c.-35_-34delinsTG ENSP00000513397.1:n.-35_-34delinsTG
ENST00000697687.1:n.363_364delinsTG
ENST00000697688.1:n.363_364delinsTG
ENST00000697689.1:c.*1020_*1021delinsTG ENSP00000513398.1:n.*1020_*1021delinsTG
ENST00000697690.1:c.317_318delinsTG ENSP00000513399.1:p.Ala106Val
ENST00000697691.1:c.*289_*290delinsTG ENSP00000513400.1:n.*289_*290delinsTG
ENST00000697692.1:c.*329_*330delinsTG ENSP00000513401.1:n.*329_*330delinsTG
ENST00000697693.1:n.1092_1093delinsTG
ENST00000697694.1:c.-35_-34delinsTG ENSP00000513402.1:n.-35_-34delinsTG
ENST00000697695.1:n.924_925delinsTG
XM_006722001.2:c.317_318delinsTG XP_006722064.1:p.Ala106Val
XM_006722001.4:c.317_318delinsTG XP_006722064.1:p.Ala106Val
XM_006722002.2:c.317_318delinsTG XP_006722065.1:p.Ala106Val
XM_006722002.4:c.317_318delinsTG XP_006722065.1:p.Ala106Val
XM_006722004.2:c.-35_-34delinsTG XP_006722067.1:n.-35_-34delinsTG
XM_006722004.3:c.-35_-34delinsTG XP_006722067.1:n.-35_-34delinsTG
XM_006722005.2:c.-35_-34delinsTG XP_006722068.1:n.-35_-34delinsTG
XM_006722005.3:c.-35_-34delinsTG XP_006722068.1:n.-35_-34delinsTG
XM_011525092.1:c.-35_-34delinsTG XP_011523394.1:n.-35_-34delinsTG
XM_011525092.2:c.-35_-34delinsTG XP_011523394.1:n.-35_-34delinsTG
XM_011525093.1:c.-35_-34delinsTG XP_011523395.1:n.-35_-34delinsTG
XM_011525093.2:c.-35_-34delinsTG XP_011523395.1:n.-35_-34delinsTG
XM_011525094.1:c.-35_-34delinsTG XP_011523396.1:n.-35_-34delinsTG
XM_011525094.2:c.-35_-34delinsTG XP_011523396.1:n.-35_-34delinsTG
XM_017024914.1:c.-35_-34delinsTG XP_016880403.1:n.-35_-34delinsTG
XM_017024915.1:c.-35_-34delinsTG XP_016880404.1:n.-35_-34delinsTG
XM_017024916.1:c.-35_-34delinsTG XP_016880405.1:n.-35_-34delinsTG
XM_017024917.1:c.-35_-34delinsTG XP_016880406.1:n.-35_-34delinsTG
XM_017024918.2:c.-35_-34delinsTG XP_016880407.1:n.-35_-34delinsTG
XM_017024919.1:c.-35_-34delinsTG XP_016880408.1:n.-35_-34delinsTG
XR_934513.1:n.390_391delinsTG
XR_934513.3:n.821_822delinsTG
XR_934514.1:n.390_391delinsTG
XR_934514.3:n.821_822delinsTG