Canonical Allele Identifier: CA3261179638
Community Standard Title: NM_058216.3(RAD51C):c.647_648delinsGT (p.Tyr216Cys)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703271_58703272delinsGT , CM000679.2:g.58703271_58703272delinsGT GRCh38
NC_000017.10:g.56780632_56780633delinsGT , CM000679.1:g.56780632_56780633delinsGT GRCh37
NC_000017.9:g.54135631_54135632delinsGT NCBI36
NG_023199.1:g.15670_15671delinsGT , LRG_314:g.15670_15671delinsGT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.647_648delinsGT MANE Select NP_478123.1:p.Tyr216Cys
ENST00000337432.9:c.647_648delinsGT MANE Select ENSP00000336701.4:p.Tyr216Cys
NM_058216.2:c.647_648delinsGT NP_478123.1:p.Tyr216Cys
NR_103872.1:n.551_552delinsGT
NR_103872.2:n.522_523delinsGT
ENST00000337432.8:c.647_648delinsGT ENSP00000336701.4:p.Tyr216Cys
ENST00000413590.5:c.285_286delinsGT
ENST00000425173.5:c.443_444delinsGT ENSP00000407282.1:p.Tyr148Cys
ENST00000461271.5:c.296_297delinsGT ENSP00000464056.1:p.Tyr99Cys
ENST00000461271.6:c.296_297delinsGT ENSP00000464056.2:p.Tyr99Cys
ENST00000475762.5:c.*1350_*1351delinsGT ENSP00000432421.1:n.*1350_*1351delinsGT
ENST00000482007.5:c.*75_*76delinsGT ENSP00000433332.1:n.*75_*76delinsGT
ENST00000487525.5:c.*75_*76delinsGT ENSP00000431637.1:n.*75_*76delinsGT
ENST00000487921.5:n.559_560delinsGT
ENST00000583539.5:c.647_648delinsGT ENSP00000463121.1:p.Tyr216Cys
ENST00000584617.5:c.369_370delinsGT
ENST00000697677.1:n.1728_1729delinsGT
ENST00000697678.1:n.549_550delinsGT
ENST00000697679.1:n.1721_1722delinsGT
ENST00000697680.1:c.*1511_*1512delinsGT ENSP00000513392.1:n.*1511_*1512delinsGT
ENST00000697681.1:c.*1663_*1664delinsGT ENSP00000513393.1:n.*1663_*1664delinsGT
ENST00000697683.1:c.*1511_*1512delinsGT ENSP00000513395.1:n.*1511_*1512delinsGT
ENST00000697684.1:n.707_708delinsGT
ENST00000697685.1:c.*1344_*1345delinsGT ENSP00000513396.1:n.*1344_*1345delinsGT
ENST00000697686.1:c.296_297delinsGT ENSP00000513397.1:p.Tyr99Cys
ENST00000697687.1:n.526_527delinsGT
ENST00000697688.1:n.693_694delinsGT
ENST00000697689.1:c.*1183_*1184delinsGT ENSP00000513398.1:n.*1183_*1184delinsGT
ENST00000697690.1:c.647_648delinsGT ENSP00000513399.1:p.Tyr216Cys
ENST00000697691.1:c.*619_*620delinsGT ENSP00000513400.1:n.*619_*620delinsGT
ENST00000697692.1:c.*659_*660delinsGT ENSP00000513401.1:n.*659_*660delinsGT
ENST00000697694.1:c.296_297delinsGT ENSP00000513402.1:p.Tyr99Cys
ENST00000697695.1:n.1254_1255delinsGT
XM_006722001.2:c.647_648delinsGT XP_006722064.1:p.Tyr216Cys
XM_006722001.4:c.647_648delinsGT XP_006722064.1:p.Tyr216Cys
XM_006722002.2:c.647_648delinsGT XP_006722065.1:p.Tyr216Cys
XM_006722002.4:c.647_648delinsGT XP_006722065.1:p.Tyr216Cys
XM_006722004.2:c.296_297delinsGT XP_006722067.1:p.Tyr99Cys
XM_006722004.3:c.296_297delinsGT XP_006722067.1:p.Tyr99Cys
XM_006722005.2:c.296_297delinsGT XP_006722068.1:p.Tyr99Cys
XM_006722005.3:c.296_297delinsGT XP_006722068.1:p.Tyr99Cys
XM_011525092.1:c.296_297delinsGT XP_011523394.1:p.Tyr99Cys
XM_011525092.2:c.296_297delinsGT XP_011523394.1:p.Tyr99Cys
XM_011525093.1:c.296_297delinsGT XP_011523395.1:p.Tyr99Cys
XM_011525093.2:c.296_297delinsGT XP_011523395.1:p.Tyr99Cys
XM_011525094.1:c.296_297delinsGT XP_011523396.1:p.Tyr99Cys
XM_011525094.2:c.296_297delinsGT XP_011523396.1:p.Tyr99Cys
XM_017024914.1:c.296_297delinsGT XP_016880403.1:p.Tyr99Cys
XM_017024915.1:c.296_297delinsGT XP_016880404.1:p.Tyr99Cys
XM_017024916.1:c.296_297delinsGT XP_016880405.1:p.Tyr99Cys
XM_017024917.1:c.296_297delinsGT XP_016880406.1:p.Tyr99Cys
XM_017024918.2:c.296_297delinsGT XP_016880407.1:p.Tyr99Cys
XM_017024919.1:c.296_297delinsGT XP_016880408.1:p.Tyr99Cys
XR_934513.1:n.720_721delinsGT
XR_934513.3:n.1151_1152delinsGT
XR_934514.1:n.720_721delinsGT
XR_934514.3:n.1151_1152delinsGT