Canonical Allele Identifier: CA3261178671
Community Standard Title: NM_058216.3(RAD51C):c.293_294delinsCT (p.Gly98Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695078_58695079delinsCT , CM000679.2:g.58695078_58695079delinsCT GRCh38
NC_000017.10:g.56772439_56772440delinsCT , CM000679.1:g.56772439_56772440delinsCT GRCh37
NC_000017.9:g.54127438_54127439delinsCT NCBI36
NG_023199.1:g.7477_7478delinsCT , LRG_314:g.7477_7478delinsCT
NG_047169.1:g.2001_2002delinsAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.293_294delinsCT MANE Select NP_478123.1:p.Gly98Ala
ENST00000337432.9:c.293_294delinsCT MANE Select ENSP00000336701.4:p.Gly98Ala
NM_002876.3:c.293_294delinsCT NP_002867.1:p.Gly98Ala
NM_002876.4:c.293_294delinsCT NP_002867.1:p.Gly98Ala
NM_058216.2:c.293_294delinsCT NP_478123.1:p.Gly98Ala
NR_103872.1:n.364_365delinsCT
NR_103872.2:n.335_336delinsCT
NR_103873.1:n.261_262delinsCT
ENST00000337432.8:c.293_294delinsCT ENSP00000336701.4:p.Gly98Ala
ENST00000421782.3:c.293_294delinsCT ENSP00000391450.2:p.Gly98Ala
ENST00000425173.5:c.89_90delinsCT ENSP00000407282.1:p.Gly30Ala
ENST00000461271.5:c.-59_-58delinsCT ENSP00000464056.1:n.-59_-58delinsCT
ENST00000461271.6:c.-59_-58delinsCT ENSP00000464056.2:n.-59_-58delinsCT
ENST00000475762.5:c.*996_*997delinsCT ENSP00000432421.1:n.*996_*997delinsCT
ENST00000482007.5:c.293_294delinsCT ENSP00000433332.1:p.Gly98Ala
ENST00000486827.1:c.*1157_*1158delinsCT ENSP00000436761.1:n.*1157_*1158delinsCT
ENST00000487525.5:c.293_294delinsCT ENSP00000431637.1:p.Gly98Ala
ENST00000487921.5:n.205_206delinsCT
ENST00000583539.5:c.293_294delinsCT ENSP00000463121.1:p.Gly98Ala
ENST00000584617.5:c.127-1615_127-1614delinsCT
ENST00000622327.4:c.29_30delinsCT ENSP00000482326.1:p.Gly10Ala
ENST00000697675.1:n.1387_1388delinsCT
ENST00000697676.1:n.353_354delinsCT
ENST00000697677.1:n.1374_1375delinsCT
ENST00000697678.1:n.195_196delinsCT
ENST00000697679.1:n.1367_1368delinsCT
ENST00000697680.1:c.*1157_*1158delinsCT ENSP00000513392.1:n.*1157_*1158delinsCT
ENST00000697681.1:c.*1157_*1158delinsCT ENSP00000513393.1:n.*1157_*1158delinsCT
ENST00000697683.1:c.*1157_*1158delinsCT ENSP00000513395.1:n.*1157_*1158delinsCT
ENST00000697684.1:n.353_354delinsCT
ENST00000697685.1:c.*1157_*1158delinsCT ENSP00000513396.1:n.*1157_*1158delinsCT
ENST00000697686.1:c.-59_-58delinsCT ENSP00000513397.1:n.-59_-58delinsCT
ENST00000697687.1:n.339_340delinsCT
ENST00000697688.1:n.339_340delinsCT
ENST00000697689.1:c.*996_*997delinsCT ENSP00000513398.1:n.*996_*997delinsCT
ENST00000697690.1:c.293_294delinsCT ENSP00000513399.1:p.Gly98Ala
ENST00000697691.1:c.*265_*266delinsCT ENSP00000513400.1:n.*265_*266delinsCT
ENST00000697692.1:c.*305_*306delinsCT ENSP00000513401.1:n.*305_*306delinsCT
ENST00000697693.1:n.1068_1069delinsCT
ENST00000697694.1:c.-59_-58delinsCT ENSP00000513402.1:n.-59_-58delinsCT
ENST00000697695.1:n.900_901delinsCT
XM_006722001.2:c.293_294delinsCT XP_006722064.1:p.Gly98Ala
XM_006722001.4:c.293_294delinsCT XP_006722064.1:p.Gly98Ala
XM_006722002.2:c.293_294delinsCT XP_006722065.1:p.Gly98Ala
XM_006722002.4:c.293_294delinsCT XP_006722065.1:p.Gly98Ala
XM_006722004.2:c.-59_-58delinsCT XP_006722067.1:n.-59_-58delinsCT
XM_006722004.3:c.-59_-58delinsCT XP_006722067.1:n.-59_-58delinsCT
XM_006722005.2:c.-59_-58delinsCT XP_006722068.1:n.-59_-58delinsCT
XM_006722005.3:c.-59_-58delinsCT XP_006722068.1:n.-59_-58delinsCT
XM_011525092.1:c.-59_-58delinsCT XP_011523394.1:n.-59_-58delinsCT
XM_011525092.2:c.-59_-58delinsCT XP_011523394.1:n.-59_-58delinsCT
XM_011525093.1:c.-59_-58delinsCT XP_011523395.1:n.-59_-58delinsCT
XM_011525093.2:c.-59_-58delinsCT XP_011523395.1:n.-59_-58delinsCT
XM_011525094.1:c.-59_-58delinsCT XP_011523396.1:n.-59_-58delinsCT
XM_011525094.2:c.-59_-58delinsCT XP_011523396.1:n.-59_-58delinsCT
XM_017024914.1:c.-59_-58delinsCT XP_016880403.1:n.-59_-58delinsCT
XM_017024915.1:c.-59_-58delinsCT XP_016880404.1:n.-59_-58delinsCT
XM_017024916.1:c.-59_-58delinsCT XP_016880405.1:n.-59_-58delinsCT
XM_017024917.1:c.-59_-58delinsCT XP_016880406.1:n.-59_-58delinsCT
XM_017024918.2:c.-59_-58delinsCT XP_016880407.1:n.-59_-58delinsCT
XM_017024919.1:c.-59_-58delinsCT XP_016880408.1:n.-59_-58delinsCT
XR_934513.1:n.366_367delinsCT
XR_934513.3:n.797_798delinsCT
XR_934514.1:n.366_367delinsCT
XR_934514.3:n.797_798delinsCT