Canonical Allele Identifier: CA3261179286
Community Standard Title: NM_058216.3(RAD51C):c.748_750delinsTAC (p.His250Tyr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709901_58709903delinsTAC , CM000679.2:g.58709901_58709903delinsTAC GRCh38
NC_000017.10:g.56787262_56787264delinsTAC , CM000679.1:g.56787262_56787264delinsTAC GRCh37
NC_000017.9:g.54142261_54142263delinsTAC NCBI36
NG_023199.1:g.22300_22302delinsTAC , LRG_314:g.22300_22302delinsTAC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.748_750delinsTAC MANE Select NP_478123.1:p.His250Tyr
ENST00000337432.9:c.748_750delinsTAC MANE Select ENSP00000336701.4:p.His250Tyr
NM_058216.2:c.748_750delinsTAC NP_478123.1:p.His250Tyr
NR_103872.1:n.652_654delinsTAC
NR_103872.2:n.623_625delinsTAC
ENST00000337432.8:c.748_750delinsTAC ENSP00000336701.4:p.His250Tyr
ENST00000413590.5:c.386_388delinsTAC
ENST00000461271.5:c.397_399delinsTAC ENSP00000464056.1:p.His133Tyr
ENST00000461271.6:c.397_399delinsTAC ENSP00000464056.2:p.His133Tyr
ENST00000475762.5:c.*1451_*1453delinsTAC ENSP00000432421.1:n.*1451_*1453delinsTAC
ENST00000482007.5:c.*176_*178delinsTAC ENSP00000433332.1:n.*176_*178delinsTAC
ENST00000487525.5:c.*321_*323delinsTAC ENSP00000431637.1:n.*321_*323delinsTAC
ENST00000578151.1:n.83_85delinsTAC
ENST00000581221.5:n.263_265delinsTAC
ENST00000583539.5:c.748_750delinsTAC ENSP00000463121.1:p.His250Tyr
ENST00000584617.5:c.470_472delinsTAC
ENST00000584804.1:c.43_45delinsTAC ENSP00000463658.1:p.His15Tyr
ENST00000697678.1:n.650_652delinsTAC
ENST00000697679.1:n.1822_1824delinsTAC
ENST00000697680.1:c.*1612_*1614delinsTAC ENSP00000513392.1:n.*1612_*1614delinsTAC
ENST00000697681.1:c.*1909_*1911delinsTAC ENSP00000513393.1:n.*1909_*1911delinsTAC
ENST00000697683.1:c.*1612_*1614delinsTAC ENSP00000513395.1:n.*1612_*1614delinsTAC
ENST00000697684.1:n.808_810delinsTAC
ENST00000697685.1:c.*1445_*1447delinsTAC ENSP00000513396.1:n.*1445_*1447delinsTAC
ENST00000697686.1:c.397_399delinsTAC ENSP00000513397.1:p.His133Tyr
ENST00000697687.1:n.627_629delinsTAC
ENST00000697688.1:n.794_796delinsTAC
ENST00000697689.1:c.*1284_*1286delinsTAC ENSP00000513398.1:n.*1284_*1286delinsTAC
ENST00000697690.1:c.748_750delinsTAC ENSP00000513399.1:p.His250Tyr
ENST00000697691.1:c.*720_*722delinsTAC ENSP00000513400.1:n.*720_*722delinsTAC
ENST00000697692.1:c.*760_*762delinsTAC ENSP00000513401.1:n.*760_*762delinsTAC
ENST00000697694.1:c.397_399delinsTAC ENSP00000513402.1:p.His133Tyr
ENST00000697695.1:n.1355_1357delinsTAC
XM_006722001.2:c.748_750delinsTAC XP_006722064.1:p.His250Tyr
XM_006722001.4:c.748_750delinsTAC XP_006722064.1:p.His250Tyr
XM_006722002.2:c.748_750delinsTAC XP_006722065.1:p.His250Tyr
XM_006722002.4:c.748_750delinsTAC XP_006722065.1:p.His250Tyr
XM_006722004.2:c.397_399delinsTAC XP_006722067.1:p.His133Tyr
XM_006722004.3:c.397_399delinsTAC XP_006722067.1:p.His133Tyr
XM_006722005.2:c.397_399delinsTAC XP_006722068.1:p.His133Tyr
XM_006722005.3:c.397_399delinsTAC XP_006722068.1:p.His133Tyr
XM_011525092.1:c.397_399delinsTAC XP_011523394.1:p.His133Tyr
XM_011525092.2:c.397_399delinsTAC XP_011523394.1:p.His133Tyr
XM_011525093.1:c.397_399delinsTAC XP_011523395.1:p.His133Tyr
XM_011525093.2:c.397_399delinsTAC XP_011523395.1:p.His133Tyr
XM_011525094.1:c.397_399delinsTAC XP_011523396.1:p.His133Tyr
XM_011525094.2:c.397_399delinsTAC XP_011523396.1:p.His133Tyr
XM_017024914.1:c.397_399delinsTAC XP_016880403.1:p.His133Tyr
XM_017024915.1:c.397_399delinsTAC XP_016880404.1:p.His133Tyr
XM_017024916.1:c.397_399delinsTAC XP_016880405.1:p.His133Tyr
XM_017024917.1:c.397_399delinsTAC XP_016880406.1:p.His133Tyr
XM_017024918.2:c.397_399delinsTAC XP_016880407.1:p.His133Tyr
XM_017024919.1:c.397_399delinsTAC XP_016880408.1:p.His133Tyr
XR_934513.1:n.966_968delinsTAC
XR_934513.3:n.1397_1399delinsTAC
XR_934514.1:n.966_968delinsTAC
XR_934514.3:n.1397_1399delinsTAC