Canonical Allele Identifier: CA1906045072

Gene: ZNF239

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43573202_43573203delinsAT , CM000672.2:g.43573202_43573203delinsAT	GRCh38
NC_000010.10:g.44068650_44068651delinsAT , CM000672.1:g.44068650_44068651delinsAT	GRCh37
NC_000010.9:g.43388656_43388657delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374446.7:c.-216+434_-216+435delinsAT MANE Select	ENSP00000363569.1:n.-216+434_-216+435delinsAT
ENST00000374446.6:c.-216+434_-216+435delinsAT	ENSP00000363569.1:n.-216+434_-216+435delinsAT
ENST00000426961.1:c.-216+1337_-216+1338delinsAT	ENSP00000398202.1:n.-216+1337_-216+1338delinsAT
ENST00000491188.1:n.58+1337_58+1338delinsAT
ENST00000535642.5:c.-93+1337_-93+1338delinsAT	ENSP00000443907.1:n.-93+1337_-93+1338delinsAT
NM_001099282.1:c.-216+434_-216+435delinsAT	NP_001092752.1:n.-216+434_-216+435delinsAT
NM_001099283.1:c.-93+1337_-93+1338delinsAT	NP_001092753.1:n.-93+1337_-93+1338delinsAT
NM_001099284.1:c.-216+1337_-216+1338delinsAT	NP_001092754.1:n.-216+1337_-216+1338delinsAT
XM_005271828.1:c.-216+434_-216+435delinsAT	XP_005271885.1:n.-216+434_-216+435delinsAT
XM_005271829.1:c.-216+1268_-216+1269delinsAT	XP_005271886.1:n.-216+1268_-216+1269delinsAT
XM_005271831.1:c.-93+1268_-93+1269delinsAT	XP_005271888.1:n.-93+1268_-93+1269delinsAT
XM_006718002.1:c.-93+434_-93+435delinsAT	XP_006718065.1:n.-93+434_-93+435delinsAT
XM_006718003.2:c.-93+835_-93+836delinsAT	XP_006718066.1:n.-93+835_-93+836delinsAT
XM_011540233.1:c.-94+434_-94+435delinsAT	XP_011538535.1:n.-94+434_-94+435delinsAT
XM_011540234.1:c.-94+1337_-94+1338delinsAT	XP_011538536.1:n.-94+1337_-94+1338delinsAT
XM_011540235.1:c.-94+1268_-94+1269delinsAT	XP_011538537.1:n.-94+1268_-94+1269delinsAT
XM_011540236.1:c.-94+835_-94+836delinsAT	XP_011538538.1:n.-94+835_-94+836delinsAT
NM_001324347.1:c.-93+434_-93+435delinsAT	NP_001311276.1:n.-93+434_-93+435delinsAT
NM_001324348.1:c.-93+1268_-93+1269delinsAT	NP_001311277.1:n.-93+1268_-93+1269delinsAT
NM_001324349.1:c.-216+434_-216+435delinsAT	NP_001311278.1:n.-216+434_-216+435delinsAT
NM_001324350.1:c.-93+434_-93+435delinsAT	NP_001311279.1:n.-93+434_-93+435delinsAT
NM_001324351.1:c.-216+1268_-216+1269delinsAT	NP_001311280.1:n.-216+1268_-216+1269delinsAT
NM_001324352.1:c.-94+434_-94+435delinsAT	NP_001311281.1:n.-94+434_-94+435delinsAT
NM_001324353.1:c.15+434_15+435delinsAT	NP_001311282.1:n.15+434_15+435delinsAT
XM_006718003.3:c.-93+835_-93+836delinsAT	XP_006718066.1:n.-93+835_-93+836delinsAT
XM_011540232.3:c.-2813_-2812delinsAT	XP_011538534.1:n.-2813_-2812delinsAT
XM_011540234.2:c.-94+1337_-94+1338delinsAT	XP_011538536.1:n.-94+1337_-94+1338delinsAT
XM_011540235.2:c.-94+1268_-94+1269delinsAT	XP_011538537.1:n.-94+1268_-94+1269delinsAT
XM_011540236.2:c.-94+835_-94+836delinsAT	XP_011538538.1:n.-94+835_-94+836delinsAT
XM_017016740.1:c.-94+434_-94+435delinsAT	XP_016872229.1:n.-94+434_-94+435delinsAT
NM_001099282.2:c.-216+434_-216+435delinsAT MANE Select	NP_001092752.1:n.-216+434_-216+435delinsAT
NM_001324347.2:c.-93+434_-93+435delinsAT	NP_001311276.1:n.-93+434_-93+435delinsAT
NM_001324348.2:c.-93+1268_-93+1269delinsAT	NP_001311277.1:n.-93+1268_-93+1269delinsAT
NM_001324349.2:c.-216+434_-216+435delinsAT	NP_001311278.1:n.-216+434_-216+435delinsAT
NM_001324350.2:c.-93+434_-93+435delinsAT	NP_001311279.1:n.-93+434_-93+435delinsAT
NM_001324351.2:c.-216+1268_-216+1269delinsAT	NP_001311280.1:n.-216+1268_-216+1269delinsAT
NM_001324352.2:c.-94+434_-94+435delinsAT	NP_001311281.1:n.-94+434_-94+435delinsAT
NM_001324353.2:c.15+434_15+435delinsAT	NP_001311282.1:n.15+434_15+435delinsAT
NM_001099283.2:c.-93+1337_-93+1338delinsAT	NP_001092753.1:n.-93+1337_-93+1338delinsAT
NM_001099284.2:c.-216+1337_-216+1338delinsAT	NP_001092754.1:n.-216+1337_-216+1338delinsAT