Canonical Allele Identifier: CA3261181226
Community Standard Title: NM_058216.3(RAD51C):c.244_246delinsTAT (p.His82Tyr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695029_58695031delinsTAT , CM000679.2:g.58695029_58695031delinsTAT GRCh38
NC_000017.10:g.56772390_56772392delinsTAT , CM000679.1:g.56772390_56772392delinsTAT GRCh37
NC_000017.9:g.54127389_54127391delinsTAT NCBI36
NG_023199.1:g.7428_7430delinsTAT , LRG_314:g.7428_7430delinsTAT
NG_047169.1:g.2049_2051delinsATA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.244_246delinsTAT MANE Select NP_478123.1:p.His82Tyr
ENST00000337432.9:c.244_246delinsTAT MANE Select ENSP00000336701.4:p.His82Tyr
NM_002876.3:c.244_246delinsTAT NP_002867.1:p.His82Tyr
NM_002876.4:c.244_246delinsTAT NP_002867.1:p.His82Tyr
NM_058216.2:c.244_246delinsTAT NP_478123.1:p.His82Tyr
NR_103872.1:n.315_317delinsTAT
NR_103872.2:n.286_288delinsTAT
NR_103873.1:n.212_214delinsTAT
ENST00000337432.8:c.244_246delinsTAT ENSP00000336701.4:p.His82Tyr
ENST00000421782.3:c.244_246delinsTAT ENSP00000391450.2:p.His82Tyr
ENST00000425173.5:c.40_42delinsTAT ENSP00000407282.1:p.His14Tyr
ENST00000461271.5:c.-108_-106delinsTAT ENSP00000464056.1:n.-108_-106delinsTAT
ENST00000461271.6:c.-108_-106delinsTAT ENSP00000464056.2:n.-108_-106delinsTAT
ENST00000475762.5:c.*947_*949delinsTAT ENSP00000432421.1:n.*947_*949delinsTAT
ENST00000482007.5:c.244_246delinsTAT ENSP00000433332.1:p.His82Tyr
ENST00000486827.1:c.*1108_*1110delinsTAT ENSP00000436761.1:n.*1108_*1110delinsTAT
ENST00000487525.5:c.244_246delinsTAT ENSP00000431637.1:p.His82Tyr
ENST00000487921.5:n.156_158delinsTAT
ENST00000583539.5:c.244_246delinsTAT ENSP00000463121.1:p.His82Tyr
ENST00000584617.5:c.127-1664_127-1662delinsTAT
ENST00000697675.1:n.1338_1340delinsTAT
ENST00000697676.1:n.304_306delinsTAT
ENST00000697677.1:n.1325_1327delinsTAT
ENST00000697678.1:n.146_148delinsTAT
ENST00000697679.1:n.1318_1320delinsTAT
ENST00000697680.1:c.*1108_*1110delinsTAT ENSP00000513392.1:n.*1108_*1110delinsTAT
ENST00000697681.1:c.*1108_*1110delinsTAT ENSP00000513393.1:n.*1108_*1110delinsTAT
ENST00000697683.1:c.*1108_*1110delinsTAT ENSP00000513395.1:n.*1108_*1110delinsTAT
ENST00000697684.1:n.304_306delinsTAT
ENST00000697685.1:c.*1108_*1110delinsTAT ENSP00000513396.1:n.*1108_*1110delinsTAT
ENST00000697686.1:c.-108_-106delinsTAT ENSP00000513397.1:n.-108_-106delinsTAT
ENST00000697687.1:n.290_292delinsTAT
ENST00000697688.1:n.290_292delinsTAT
ENST00000697689.1:c.*947_*949delinsTAT ENSP00000513398.1:n.*947_*949delinsTAT
ENST00000697690.1:c.244_246delinsTAT ENSP00000513399.1:p.His82Tyr
ENST00000697691.1:c.*216_*218delinsTAT ENSP00000513400.1:n.*216_*218delinsTAT
ENST00000697692.1:c.*256_*258delinsTAT ENSP00000513401.1:n.*256_*258delinsTAT
ENST00000697693.1:n.1019_1021delinsTAT
ENST00000697694.1:c.-108_-106delinsTAT ENSP00000513402.1:n.-108_-106delinsTAT
ENST00000697695.1:n.851_853delinsTAT
XM_006722001.2:c.244_246delinsTAT XP_006722064.1:p.His82Tyr
XM_006722001.4:c.244_246delinsTAT XP_006722064.1:p.His82Tyr
XM_006722002.2:c.244_246delinsTAT XP_006722065.1:p.His82Tyr
XM_006722002.4:c.244_246delinsTAT XP_006722065.1:p.His82Tyr
XM_006722004.2:c.-108_-106delinsTAT XP_006722067.1:n.-108_-106delinsTAT
XM_006722004.3:c.-108_-106delinsTAT XP_006722067.1:n.-108_-106delinsTAT
XM_006722005.2:c.-108_-106delinsTAT XP_006722068.1:n.-108_-106delinsTAT
XM_006722005.3:c.-108_-106delinsTAT XP_006722068.1:n.-108_-106delinsTAT
XM_011525092.1:c.-108_-106delinsTAT XP_011523394.1:n.-108_-106delinsTAT
XM_011525092.2:c.-108_-106delinsTAT XP_011523394.1:n.-108_-106delinsTAT
XM_011525093.1:c.-108_-106delinsTAT XP_011523395.1:n.-108_-106delinsTAT
XM_011525093.2:c.-108_-106delinsTAT XP_011523395.1:n.-108_-106delinsTAT
XM_011525094.1:c.-108_-106delinsTAT XP_011523396.1:n.-108_-106delinsTAT
XM_011525094.2:c.-108_-106delinsTAT XP_011523396.1:n.-108_-106delinsTAT
XM_017024914.1:c.-108_-106delinsTAT XP_016880403.1:n.-108_-106delinsTAT
XM_017024915.1:c.-108_-106delinsTAT XP_016880404.1:n.-108_-106delinsTAT
XM_017024916.1:c.-108_-106delinsTAT XP_016880405.1:n.-108_-106delinsTAT
XM_017024917.1:c.-108_-106delinsTAT XP_016880406.1:n.-108_-106delinsTAT
XM_017024918.2:c.-108_-106delinsTAT XP_016880407.1:n.-108_-106delinsTAT
XM_017024919.1:c.-108_-106delinsTAT XP_016880408.1:n.-108_-106delinsTAT
XR_934513.1:n.317_319delinsTAT
XR_934513.3:n.748_750delinsTAT
XR_934514.1:n.317_319delinsTAT
XR_934514.3:n.748_750delinsTAT