Canonical Allele Identifier: CA3057243447
Community Standard Title: NM_058216.3(RAD51C):c.1000_1001delinsTG (p.Glu334Ter)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732518_58732519delinsTG , CM000679.2:g.58732518_58732519delinsTG GRCh38
NC_000017.10:g.56809879_56809880delinsTG , CM000679.1:g.56809879_56809880delinsTG GRCh37
NC_000017.9:g.54164878_54164879delinsTG NCBI36
NG_023199.1:g.44917_44918delinsTG , LRG_314:g.44917_44918delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1000_1001delinsTG MANE Select NP_478123.1:p.Glu334Ter
ENST00000337432.9:c.1000_1001delinsTG MANE Select ENSP00000336701.4:p.Glu334Ter
NM_058216.2:c.1000_1001delinsTG NP_478123.1:p.Glu334Ter
NR_103872.1:n.904_905delinsTG
NR_103872.2:n.875_876delinsTG
ENST00000337432.8:c.1000_1001delinsTG ENSP00000336701.4:p.Glu334Ter
ENST00000413590.5:c.641_642delinsTG
ENST00000461271.6:c.649_650delinsTG ENSP00000464056.2:p.Glu217Ter
ENST00000461706.1:n.187_188delinsTG
ENST00000475762.5:c.*1636_*1637delinsTG ENSP00000432421.1:n.*1636_*1637delinsTG
ENST00000482007.5:c.*428_*429delinsTG ENSP00000433332.1:n.*428_*429delinsTG
ENST00000487525.5:c.*576_*577delinsTG ENSP00000431637.1:n.*576_*577delinsTG
ENST00000578151.1:n.240-1600_240-1599delinsTG
ENST00000581221.5:n.515_516delinsTG
ENST00000583539.5:c.1000_1001delinsTG ENSP00000463121.1:p.Glu334Ter
ENST00000584617.5:c.722_723delinsTG
ENST00000584804.1:c.234_235delinsTG ENSP00000463658.1:p.Arg78_Asn79delinsSerAsp
ENST00000697680.1:c.*1964_*1965delinsTG ENSP00000513392.1:n.*1964_*1965delinsTG
ENST00000697681.1:c.*2161_*2162delinsTG ENSP00000513393.1:n.*2161_*2162delinsTG
ENST00000697683.1:c.*1936_*1937delinsTG ENSP00000513395.1:n.*1936_*1937delinsTG
ENST00000697685.1:c.*1697_*1698delinsTG ENSP00000513396.1:n.*1697_*1698delinsTG
ENST00000697686.1:c.771_772delinsTG ENSP00000513397.1:p.Arg257_Asn258delinsSerAsp
ENST00000697689.1:c.*1441-1600_*1441-1599delinsTG ENSP00000513398.1:n.*1441-1600_*1441-1599delinsTG
ENST00000697690.1:c.905-1600_905-1599delinsTG ENSP00000513399.1:n.905-1600_905-1599delinsTG
ENST00000697691.1:c.*972_*973delinsTG ENSP00000513400.1:n.*972_*973delinsTG
ENST00000697692.1:c.*1012_*1013delinsTG ENSP00000513401.1:n.*1012_*1013delinsTG
ENST00000697694.1:c.649_650delinsTG ENSP00000513402.1:p.Glu217Ter
ENST00000697695.1:n.1607_1608delinsTG
XM_006722001.2:c.1003_1004delinsTG XP_006722064.1:p.Glu335Ter
XM_006722001.4:c.1003_1004delinsTG XP_006722064.1:p.Glu335Ter
XM_006722002.2:c.939_940delinsTG XP_006722065.1:p.Arg313_Asn314delinsSerAsp
XM_006722002.4:c.939_940delinsTG XP_006722065.1:p.Arg313_Asn314delinsSerAsp
XM_006722004.2:c.652_653delinsTG XP_006722067.1:p.Glu218Ter
XM_006722004.3:c.652_653delinsTG XP_006722067.1:p.Glu218Ter
XM_006722005.2:c.652_653delinsTG XP_006722068.1:p.Glu218Ter
XM_006722005.3:c.652_653delinsTG XP_006722068.1:p.Glu218Ter
XM_011525092.1:c.652_653delinsTG XP_011523394.1:p.Glu218Ter
XM_011525092.2:c.652_653delinsTG XP_011523394.1:p.Glu218Ter
XM_011525093.1:c.652_653delinsTG XP_011523395.1:p.Glu218Ter
XM_011525093.2:c.652_653delinsTG XP_011523395.1:p.Glu218Ter
XM_011525094.1:c.652_653delinsTG XP_011523396.1:p.Glu218Ter
XM_011525094.2:c.652_653delinsTG XP_011523396.1:p.Glu218Ter
XM_017024914.1:c.649_650delinsTG XP_016880403.1:p.Glu217Ter
XM_017024915.1:c.649_650delinsTG XP_016880404.1:p.Glu217Ter
XM_017024916.1:c.649_650delinsTG XP_016880405.1:p.Glu217Ter
XM_017024917.1:c.649_650delinsTG XP_016880406.1:p.Glu217Ter
XM_017024918.2:c.649_650delinsTG XP_016880407.1:p.Glu217Ter
XM_017024919.1:c.588_589delinsTG XP_016880408.1:p.Arg196_Asn197delinsSerAsp
XR_934513.1:n.1218_1219delinsTG
XR_934513.3:n.1649_1650delinsTG
XR_934514.1:n.1221_1222delinsTG
XR_934514.3:n.1652_1653delinsTG
XR_934886.1:n.149+5552_149+5553delinsCA
XR_934886.2:n.149+5552_149+5553delinsCA