Canonical Allele Identifier: CA3261179530
Community Standard Title: NM_058216.3(RAD51C):c.760_762delinsTAT (p.Asp254Tyr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709913_58709915delinsTAT , CM000679.2:g.58709913_58709915delinsTAT GRCh38
NC_000017.10:g.56787274_56787276delinsTAT , CM000679.1:g.56787274_56787276delinsTAT GRCh37
NC_000017.9:g.54142273_54142275delinsTAT NCBI36
NG_023199.1:g.22312_22314delinsTAT , LRG_314:g.22312_22314delinsTAT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.760_762delinsTAT MANE Select NP_478123.1:p.Asp254Tyr
ENST00000337432.9:c.760_762delinsTAT MANE Select ENSP00000336701.4:p.Asp254Tyr
NM_058216.2:c.760_762delinsTAT NP_478123.1:p.Asp254Tyr
NR_103872.1:n.664_666delinsTAT
NR_103872.2:n.635_637delinsTAT
ENST00000337432.8:c.760_762delinsTAT ENSP00000336701.4:p.Asp254Tyr
ENST00000413590.5:c.398_400delinsTAT
ENST00000461271.6:c.409_411delinsTAT ENSP00000464056.2:p.Asp137Tyr
ENST00000475762.5:c.*1463_*1465delinsTAT ENSP00000432421.1:n.*1463_*1465delinsTAT
ENST00000482007.5:c.*188_*190delinsTAT ENSP00000433332.1:n.*188_*190delinsTAT
ENST00000487525.5:c.*333_*335delinsTAT ENSP00000431637.1:n.*333_*335delinsTAT
ENST00000578151.1:n.95_97delinsTAT
ENST00000581221.5:n.275_277delinsTAT
ENST00000583539.5:c.760_762delinsTAT ENSP00000463121.1:p.Asp254Tyr
ENST00000584617.5:c.482_484delinsTAT
ENST00000584804.1:c.55_57delinsTAT ENSP00000463658.1:p.Asp19Tyr
ENST00000697678.1:n.662_664delinsTAT
ENST00000697679.1:n.1834_1836delinsTAT
ENST00000697680.1:c.*1624_*1626delinsTAT ENSP00000513392.1:n.*1624_*1626delinsTAT
ENST00000697681.1:c.*1921_*1923delinsTAT ENSP00000513393.1:n.*1921_*1923delinsTAT
ENST00000697683.1:c.*1624_*1626delinsTAT ENSP00000513395.1:n.*1624_*1626delinsTAT
ENST00000697684.1:n.820_822delinsTAT
ENST00000697685.1:c.*1457_*1459delinsTAT ENSP00000513396.1:n.*1457_*1459delinsTAT
ENST00000697686.1:c.409_411delinsTAT ENSP00000513397.1:p.Asp137Tyr
ENST00000697687.1:n.639_641delinsTAT
ENST00000697688.1:n.806_808delinsTAT
ENST00000697689.1:c.*1296_*1298delinsTAT ENSP00000513398.1:n.*1296_*1298delinsTAT
ENST00000697690.1:c.760_762delinsTAT ENSP00000513399.1:p.Asp254Tyr
ENST00000697691.1:c.*732_*734delinsTAT ENSP00000513400.1:n.*732_*734delinsTAT
ENST00000697692.1:c.*772_*774delinsTAT ENSP00000513401.1:n.*772_*774delinsTAT
ENST00000697694.1:c.409_411delinsTAT ENSP00000513402.1:p.Asp137Tyr
ENST00000697695.1:n.1367_1369delinsTAT
XM_006722001.2:c.760_762delinsTAT XP_006722064.1:p.Asp254Tyr
XM_006722001.4:c.760_762delinsTAT XP_006722064.1:p.Asp254Tyr
XM_006722002.2:c.760_762delinsTAT XP_006722065.1:p.Asp254Tyr
XM_006722002.4:c.760_762delinsTAT XP_006722065.1:p.Asp254Tyr
XM_006722004.2:c.409_411delinsTAT XP_006722067.1:p.Asp137Tyr
XM_006722004.3:c.409_411delinsTAT XP_006722067.1:p.Asp137Tyr
XM_006722005.2:c.409_411delinsTAT XP_006722068.1:p.Asp137Tyr
XM_006722005.3:c.409_411delinsTAT XP_006722068.1:p.Asp137Tyr
XM_011525092.1:c.409_411delinsTAT XP_011523394.1:p.Asp137Tyr
XM_011525092.2:c.409_411delinsTAT XP_011523394.1:p.Asp137Tyr
XM_011525093.1:c.409_411delinsTAT XP_011523395.1:p.Asp137Tyr
XM_011525093.2:c.409_411delinsTAT XP_011523395.1:p.Asp137Tyr
XM_011525094.1:c.409_411delinsTAT XP_011523396.1:p.Asp137Tyr
XM_011525094.2:c.409_411delinsTAT XP_011523396.1:p.Asp137Tyr
XM_017024914.1:c.409_411delinsTAT XP_016880403.1:p.Asp137Tyr
XM_017024915.1:c.409_411delinsTAT XP_016880404.1:p.Asp137Tyr
XM_017024916.1:c.409_411delinsTAT XP_016880405.1:p.Asp137Tyr
XM_017024917.1:c.409_411delinsTAT XP_016880406.1:p.Asp137Tyr
XM_017024918.2:c.409_411delinsTAT XP_016880407.1:p.Asp137Tyr
XM_017024919.1:c.409_411delinsTAT XP_016880408.1:p.Asp137Tyr
XR_934513.1:n.978_980delinsTAT
XR_934513.3:n.1409_1411delinsTAT
XR_934514.1:n.978_980delinsTAT
XR_934514.3:n.1409_1411delinsTAT