Canonical Allele Identifier: CA1906045094

Gene: ZNF239

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43573220_43573222delinsAAT , CM000672.2:g.43573220_43573222delinsAAT	GRCh38
NC_000010.10:g.44068668_44068670delinsAAT , CM000672.1:g.44068668_44068670delinsAAT	GRCh37
NC_000010.9:g.43388674_43388676delinsAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374446.7:c.-216+415_-216+417delinsATT MANE Select	ENSP00000363569.1:n.-216+415_-216+417delinsATT
ENST00000374446.6:c.-216+415_-216+417delinsATT	ENSP00000363569.1:n.-216+415_-216+417delinsATT
ENST00000426961.1:c.-216+1318_-216+1320delinsATT	ENSP00000398202.1:n.-216+1318_-216+1320delinsATT
ENST00000491188.1:n.58+1318_58+1320delinsATT
ENST00000535642.5:c.-93+1318_-93+1320delinsATT	ENSP00000443907.1:n.-93+1318_-93+1320delinsATT
NM_001099282.1:c.-216+415_-216+417delinsATT	NP_001092752.1:n.-216+415_-216+417delinsATT
NM_001099283.1:c.-93+1318_-93+1320delinsATT	NP_001092753.1:n.-93+1318_-93+1320delinsATT
NM_001099284.1:c.-216+1318_-216+1320delinsATT	NP_001092754.1:n.-216+1318_-216+1320delinsATT
XM_005271828.1:c.-216+415_-216+417delinsATT	XP_005271885.1:n.-216+415_-216+417delinsATT
XM_005271829.1:c.-216+1249_-216+1251delinsATT	XP_005271886.1:n.-216+1249_-216+1251delinsATT
XM_005271831.1:c.-93+1249_-93+1251delinsATT	XP_005271888.1:n.-93+1249_-93+1251delinsATT
XM_006718002.1:c.-93+415_-93+417delinsATT	XP_006718065.1:n.-93+415_-93+417delinsATT
XM_006718003.2:c.-93+816_-93+818delinsATT	XP_006718066.1:n.-93+816_-93+818delinsATT
XM_011540233.1:c.-94+415_-94+417delinsATT	XP_011538535.1:n.-94+415_-94+417delinsATT
XM_011540234.1:c.-94+1318_-94+1320delinsATT	XP_011538536.1:n.-94+1318_-94+1320delinsATT
XM_011540235.1:c.-94+1249_-94+1251delinsATT	XP_011538537.1:n.-94+1249_-94+1251delinsATT
XM_011540236.1:c.-94+816_-94+818delinsATT	XP_011538538.1:n.-94+816_-94+818delinsATT
NM_001324347.1:c.-93+415_-93+417delinsATT	NP_001311276.1:n.-93+415_-93+417delinsATT
NM_001324348.1:c.-93+1249_-93+1251delinsATT	NP_001311277.1:n.-93+1249_-93+1251delinsATT
NM_001324349.1:c.-216+415_-216+417delinsATT	NP_001311278.1:n.-216+415_-216+417delinsATT
NM_001324350.1:c.-93+415_-93+417delinsATT	NP_001311279.1:n.-93+415_-93+417delinsATT
NM_001324351.1:c.-216+1249_-216+1251delinsATT	NP_001311280.1:n.-216+1249_-216+1251delinsATT
NM_001324352.1:c.-94+415_-94+417delinsATT	NP_001311281.1:n.-94+415_-94+417delinsATT
NM_001324353.1:c.15+415_15+417delinsATT	NP_001311282.1:n.15+415_15+417delinsATT
XM_006718003.3:c.-93+816_-93+818delinsATT	XP_006718066.1:n.-93+816_-93+818delinsATT
XM_011540232.3:c.-2832_-2830delinsATT	XP_011538534.1:n.-2832_-2830delinsATT
XM_011540234.2:c.-94+1318_-94+1320delinsATT	XP_011538536.1:n.-94+1318_-94+1320delinsATT
XM_011540235.2:c.-94+1249_-94+1251delinsATT	XP_011538537.1:n.-94+1249_-94+1251delinsATT
XM_011540236.2:c.-94+816_-94+818delinsATT	XP_011538538.1:n.-94+816_-94+818delinsATT
XM_017016740.1:c.-94+415_-94+417delinsATT	XP_016872229.1:n.-94+415_-94+417delinsATT
NM_001099282.2:c.-216+415_-216+417delinsATT MANE Select	NP_001092752.1:n.-216+415_-216+417delinsATT
NM_001324347.2:c.-93+415_-93+417delinsATT	NP_001311276.1:n.-93+415_-93+417delinsATT
NM_001324348.2:c.-93+1249_-93+1251delinsATT	NP_001311277.1:n.-93+1249_-93+1251delinsATT
NM_001324349.2:c.-216+415_-216+417delinsATT	NP_001311278.1:n.-216+415_-216+417delinsATT
NM_001324350.2:c.-93+415_-93+417delinsATT	NP_001311279.1:n.-93+415_-93+417delinsATT
NM_001324351.2:c.-216+1249_-216+1251delinsATT	NP_001311280.1:n.-216+1249_-216+1251delinsATT
NM_001324352.2:c.-94+415_-94+417delinsATT	NP_001311281.1:n.-94+415_-94+417delinsATT
NM_001324353.2:c.15+415_15+417delinsATT	NP_001311282.1:n.15+415_15+417delinsATT
NM_001099283.2:c.-93+1318_-93+1320delinsATT	NP_001092753.1:n.-93+1318_-93+1320delinsATT
NM_001099284.2:c.-216+1318_-216+1320delinsATT	NP_001092754.1:n.-216+1318_-216+1320delinsATT