Canonical Allele Identifier: CA1906044956
Gene: ZNF239 HGNC NCBI

Linked Data

dbSNP Id: rs1838132305

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43573067_43573070del , CM000672.2:g.43573067_43573070del GRCh38
NC_000010.10:g.44068515_44068518del , CM000672.1:g.44068515_44068518del GRCh37
NC_000010.9:g.43388521_43388524del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374446.7:c.-216+569_-216+572del MANE Select ENSP00000363569.1:n.-216+569_-216+572del
ENST00000374446.6:c.-216+569_-216+572del ENSP00000363569.1:n.-216+569_-216+572del
ENST00000426961.1:c.-216+1472_-216+1475del ENSP00000398202.1:n.-216+1472_-216+1475de...
ENST00000491188.1:n.58+1472_58+1475del
ENST00000535642.5:c.-93+1472_-93+1475del ENSP00000443907.1:n.-93+1472_-93+1475del
NM_001099282.1:c.-216+569_-216+572del NP_001092752.1:n.-216+569_-216+572del
NM_001099283.1:c.-93+1472_-93+1475del NP_001092753.1:n.-93+1472_-93+1475del
NM_001099284.1:c.-216+1472_-216+1475del NP_001092754.1:n.-216+1472_-216+1475del
XM_005271828.1:c.-216+569_-216+572del XP_005271885.1:n.-216+569_-216+572del
XM_005271829.1:c.-216+1403_-216+1406del XP_005271886.1:n.-216+1403_-216+1406del
XM_005271831.1:c.-93+1403_-93+1406del XP_005271888.1:n.-93+1403_-93+1406del
XM_006718002.1:c.-93+569_-93+572del XP_006718065.1:n.-93+569_-93+572del
XM_006718003.2:c.-93+970_-93+973del XP_006718066.1:n.-93+970_-93+973del
XM_011540233.1:c.-94+569_-94+572del XP_011538535.1:n.-94+569_-94+572del
XM_011540234.1:c.-94+1472_-94+1475del XP_011538536.1:n.-94+1472_-94+1475del
XM_011540235.1:c.-94+1403_-94+1406del XP_011538537.1:n.-94+1403_-94+1406del
XM_011540236.1:c.-94+970_-94+973del XP_011538538.1:n.-94+970_-94+973del
NM_001324347.1:c.-93+569_-93+572del NP_001311276.1:n.-93+569_-93+572del
NM_001324348.1:c.-93+1403_-93+1406del NP_001311277.1:n.-93+1403_-93+1406del
NM_001324349.1:c.-216+569_-216+572del NP_001311278.1:n.-216+569_-216+572del
NM_001324350.1:c.-93+569_-93+572del NP_001311279.1:n.-93+569_-93+572del
NM_001324351.1:c.-216+1403_-216+1406del NP_001311280.1:n.-216+1403_-216+1406del
NM_001324352.1:c.-94+569_-94+572del NP_001311281.1:n.-94+569_-94+572del
NM_001324353.1:c.15+569_15+572del NP_001311282.1:n.15+569_15+572del
XM_006718003.3:c.-93+970_-93+973del XP_006718066.1:n.-93+970_-93+973del
XM_011540232.3:c.-2678_-2675del XP_011538534.1:n.-2678_-2675del
XM_011540234.2:c.-94+1472_-94+1475del XP_011538536.1:n.-94+1472_-94+1475del
XM_011540235.2:c.-94+1403_-94+1406del XP_011538537.1:n.-94+1403_-94+1406del
XM_011540236.2:c.-94+970_-94+973del XP_011538538.1:n.-94+970_-94+973del
XM_017016740.1:c.-94+569_-94+572del XP_016872229.1:n.-94+569_-94+572del
NM_001099282.2:c.-216+569_-216+572del MANE Select NP_001092752.1:n.-216+569_-216+572del
NM_001324347.2:c.-93+569_-93+572del NP_001311276.1:n.-93+569_-93+572del
NM_001324348.2:c.-93+1403_-93+1406del NP_001311277.1:n.-93+1403_-93+1406del
NM_001324349.2:c.-216+569_-216+572del NP_001311278.1:n.-216+569_-216+572del
NM_001324350.2:c.-93+569_-93+572del NP_001311279.1:n.-93+569_-93+572del
NM_001324351.2:c.-216+1403_-216+1406del NP_001311280.1:n.-216+1403_-216+1406del
NM_001324352.2:c.-94+569_-94+572del NP_001311281.1:n.-94+569_-94+572del
NM_001324353.2:c.15+569_15+572del NP_001311282.1:n.15+569_15+572del
NM_001099283.2:c.-93+1472_-93+1475del NP_001092753.1:n.-93+1472_-93+1475del
NM_001099284.2:c.-216+1472_-216+1475del NP_001092754.1:n.-216+1472_-216+1475del