Canonical Allele Identifier: CA3261179654
Community Standard Title: NM_058216.3(RAD51C):c.649_651delinsCCC (p.Thr217Pro)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703273_58703275delinsCCC , CM000679.2:g.58703273_58703275delinsCCC GRCh38
NC_000017.10:g.56780634_56780636delinsCCC , CM000679.1:g.56780634_56780636delinsCCC GRCh37
NC_000017.9:g.54135633_54135635delinsCCC NCBI36
NG_023199.1:g.15672_15674delinsCCC , LRG_314:g.15672_15674delinsCCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.649_651delinsCCC MANE Select NP_478123.1:p.Thr217Pro
ENST00000337432.9:c.649_651delinsCCC MANE Select ENSP00000336701.4:p.Thr217Pro
NM_058216.2:c.649_651delinsCCC NP_478123.1:p.Thr217Pro
NR_103872.1:n.553_555delinsCCC
NR_103872.2:n.524_526delinsCCC
ENST00000337432.8:c.649_651delinsCCC ENSP00000336701.4:p.Thr217Pro
ENST00000413590.5:c.287_289delinsCCC
ENST00000425173.5:c.445_447delinsCCC ENSP00000407282.1:p.Thr149Pro
ENST00000461271.5:c.298_300delinsCCC ENSP00000464056.1:p.Thr100Pro
ENST00000461271.6:c.298_300delinsCCC ENSP00000464056.2:p.Thr100Pro
ENST00000475762.5:c.*1352_*1354delinsCCC ENSP00000432421.1:n.*1352_*1354delinsCCC
ENST00000482007.5:c.*77_*79delinsCCC ENSP00000433332.1:n.*77_*79delinsCCC
ENST00000487525.5:c.*77_*79delinsCCC ENSP00000431637.1:n.*77_*79delinsCCC
ENST00000487921.5:n.561_563delinsCCC
ENST00000583539.5:c.649_651delinsCCC ENSP00000463121.1:p.Thr217Pro
ENST00000584617.5:c.371_373delinsCCC
ENST00000697677.1:n.1730_1732delinsCCC
ENST00000697678.1:n.551_553delinsCCC
ENST00000697679.1:n.1723_1725delinsCCC
ENST00000697680.1:c.*1513_*1515delinsCCC ENSP00000513392.1:n.*1513_*1515delinsCCC
ENST00000697681.1:c.*1665_*1667delinsCCC ENSP00000513393.1:n.*1665_*1667delinsCCC
ENST00000697683.1:c.*1513_*1515delinsCCC ENSP00000513395.1:n.*1513_*1515delinsCCC
ENST00000697684.1:n.709_711delinsCCC
ENST00000697685.1:c.*1346_*1348delinsCCC ENSP00000513396.1:n.*1346_*1348delinsCCC
ENST00000697686.1:c.298_300delinsCCC ENSP00000513397.1:p.Thr100Pro
ENST00000697687.1:n.528_530delinsCCC
ENST00000697688.1:n.695_697delinsCCC
ENST00000697689.1:c.*1185_*1187delinsCCC ENSP00000513398.1:n.*1185_*1187delinsCCC
ENST00000697690.1:c.649_651delinsCCC ENSP00000513399.1:p.Thr217Pro
ENST00000697691.1:c.*621_*623delinsCCC ENSP00000513400.1:n.*621_*623delinsCCC
ENST00000697692.1:c.*661_*663delinsCCC ENSP00000513401.1:n.*661_*663delinsCCC
ENST00000697694.1:c.298_300delinsCCC ENSP00000513402.1:p.Thr100Pro
ENST00000697695.1:n.1256_1258delinsCCC
XM_006722001.2:c.649_651delinsCCC XP_006722064.1:p.Thr217Pro
XM_006722001.4:c.649_651delinsCCC XP_006722064.1:p.Thr217Pro
XM_006722002.2:c.649_651delinsCCC XP_006722065.1:p.Thr217Pro
XM_006722002.4:c.649_651delinsCCC XP_006722065.1:p.Thr217Pro
XM_006722004.2:c.298_300delinsCCC XP_006722067.1:p.Thr100Pro
XM_006722004.3:c.298_300delinsCCC XP_006722067.1:p.Thr100Pro
XM_006722005.2:c.298_300delinsCCC XP_006722068.1:p.Thr100Pro
XM_006722005.3:c.298_300delinsCCC XP_006722068.1:p.Thr100Pro
XM_011525092.1:c.298_300delinsCCC XP_011523394.1:p.Thr100Pro
XM_011525092.2:c.298_300delinsCCC XP_011523394.1:p.Thr100Pro
XM_011525093.1:c.298_300delinsCCC XP_011523395.1:p.Thr100Pro
XM_011525093.2:c.298_300delinsCCC XP_011523395.1:p.Thr100Pro
XM_011525094.1:c.298_300delinsCCC XP_011523396.1:p.Thr100Pro
XM_011525094.2:c.298_300delinsCCC XP_011523396.1:p.Thr100Pro
XM_017024914.1:c.298_300delinsCCC XP_016880403.1:p.Thr100Pro
XM_017024915.1:c.298_300delinsCCC XP_016880404.1:p.Thr100Pro
XM_017024916.1:c.298_300delinsCCC XP_016880405.1:p.Thr100Pro
XM_017024917.1:c.298_300delinsCCC XP_016880406.1:p.Thr100Pro
XM_017024918.2:c.298_300delinsCCC XP_016880407.1:p.Thr100Pro
XM_017024919.1:c.298_300delinsCCC XP_016880408.1:p.Thr100Pro
XR_934513.1:n.722_724delinsCCC
XR_934513.3:n.1153_1155delinsCCC
XR_934514.1:n.722_724delinsCCC
XR_934514.3:n.1153_1155delinsCCC