Canonical Allele Identifier: CA3261178913
Community Standard Title: NM_058216.3(RAD51C):c.992_993delinsTT (p.Ser331Ile)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732510_58732511delinsTT , CM000679.2:g.58732510_58732511delinsTT GRCh38
NC_000017.10:g.56809871_56809872delinsTT , CM000679.1:g.56809871_56809872delinsTT GRCh37
NC_000017.9:g.54164870_54164871delinsTT NCBI36
NG_023199.1:g.44909_44910delinsTT , LRG_314:g.44909_44910delinsTT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.992_993delinsTT MANE Select NP_478123.1:p.Ser331Ile
ENST00000337432.9:c.992_993delinsTT MANE Select ENSP00000336701.4:p.Ser331Ile
NM_058216.2:c.992_993delinsTT NP_478123.1:p.Ser331Ile
NR_103872.1:n.896_897delinsTT
NR_103872.2:n.867_868delinsTT
ENST00000337432.8:c.992_993delinsTT ENSP00000336701.4:p.Ser331Ile
ENST00000413590.5:c.633_634delinsTT
ENST00000461271.6:c.641_642delinsTT ENSP00000464056.2:p.Ser214Ile
ENST00000461706.1:n.179_180delinsTT
ENST00000475762.5:c.*1628_*1629delinsTT ENSP00000432421.1:n.*1628_*1629delinsTT
ENST00000482007.5:c.*420_*421delinsTT ENSP00000433332.1:n.*420_*421delinsTT
ENST00000487525.5:c.*568_*569delinsTT ENSP00000431637.1:n.*568_*569delinsTT
ENST00000578151.1:n.240-1608_240-1607delinsTT
ENST00000581221.5:n.507_508delinsTT
ENST00000583539.5:c.992_993delinsTT ENSP00000463121.1:p.Ser331Ile
ENST00000584617.5:c.714_715delinsTT
ENST00000584804.1:c.226_227delinsTT ENSP00000463658.1:p.Ala76Phe
ENST00000697680.1:c.*1956_*1957delinsTT ENSP00000513392.1:n.*1956_*1957delinsTT
ENST00000697681.1:c.*2153_*2154delinsTT ENSP00000513393.1:n.*2153_*2154delinsTT
ENST00000697683.1:c.*1928_*1929delinsTT ENSP00000513395.1:n.*1928_*1929delinsTT
ENST00000697685.1:c.*1689_*1690delinsTT ENSP00000513396.1:n.*1689_*1690delinsTT
ENST00000697686.1:c.763_764delinsTT ENSP00000513397.1:p.Ala255Phe
ENST00000697689.1:c.*1441-1608_*1441-1607delinsTT ENSP00000513398.1:n.*1441-1608_*1441-1607delinsTT
ENST00000697690.1:c.905-1608_905-1607delinsTT ENSP00000513399.1:n.905-1608_905-1607delinsTT
ENST00000697691.1:c.*964_*965delinsTT ENSP00000513400.1:n.*964_*965delinsTT
ENST00000697692.1:c.*1004_*1005delinsTT ENSP00000513401.1:n.*1004_*1005delinsTT
ENST00000697694.1:c.641_642delinsTT ENSP00000513402.1:p.Ser214Ile
ENST00000697695.1:n.1599_1600delinsTT
XM_006722001.2:c.995_996delinsTT XP_006722064.1:p.Ser332Ile
XM_006722001.4:c.995_996delinsTT XP_006722064.1:p.Ser332Ile
XM_006722002.2:c.931_932delinsTT XP_006722065.1:p.Ala311Phe
XM_006722002.4:c.931_932delinsTT XP_006722065.1:p.Ala311Phe
XM_006722004.2:c.644_645delinsTT XP_006722067.1:p.Ser215Ile
XM_006722004.3:c.644_645delinsTT XP_006722067.1:p.Ser215Ile
XM_006722005.2:c.644_645delinsTT XP_006722068.1:p.Ser215Ile
XM_006722005.3:c.644_645delinsTT XP_006722068.1:p.Ser215Ile
XM_011525092.1:c.644_645delinsTT XP_011523394.1:p.Ser215Ile
XM_011525092.2:c.644_645delinsTT XP_011523394.1:p.Ser215Ile
XM_011525093.1:c.644_645delinsTT XP_011523395.1:p.Ser215Ile
XM_011525093.2:c.644_645delinsTT XP_011523395.1:p.Ser215Ile
XM_011525094.1:c.644_645delinsTT XP_011523396.1:p.Ser215Ile
XM_011525094.2:c.644_645delinsTT XP_011523396.1:p.Ser215Ile
XM_017024914.1:c.641_642delinsTT XP_016880403.1:p.Ser214Ile
XM_017024915.1:c.641_642delinsTT XP_016880404.1:p.Ser214Ile
XM_017024916.1:c.641_642delinsTT XP_016880405.1:p.Ser214Ile
XM_017024917.1:c.641_642delinsTT XP_016880406.1:p.Ser214Ile
XM_017024918.2:c.641_642delinsTT XP_016880407.1:p.Ser214Ile
XM_017024919.1:c.580_581delinsTT XP_016880408.1:p.Ala194Phe
XR_934513.1:n.1210_1211delinsTT
XR_934513.3:n.1641_1642delinsTT
XR_934514.1:n.1213_1214delinsTT
XR_934514.3:n.1644_1645delinsTT
XR_934886.1:n.149+5560_149+5561delinsAA
XR_934886.2:n.149+5560_149+5561delinsAA