Canonical Allele Identifier: CA1906044970

Gene: ZNF239

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43573076_43573078delinsCAG , CM000672.2:g.43573076_43573078delinsCAG	GRCh38
NC_000010.10:g.44068524_44068526delinsCAG , CM000672.1:g.44068524_44068526delinsCAG	GRCh37
NC_000010.9:g.43388530_43388532delinsCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374446.7:c.-216+559_-216+561delinsCTG MANE Select	ENSP00000363569.1:n.-216+559_-216+561delinsCTG
ENST00000374446.6:c.-216+559_-216+561delinsCTG	ENSP00000363569.1:n.-216+559_-216+561delinsCTG
ENST00000426961.1:c.-216+1462_-216+1464delinsCTG	ENSP00000398202.1:n.-216+1462_-216+1464delinsCTG
ENST00000491188.1:n.58+1462_58+1464delinsCTG
ENST00000535642.5:c.-93+1462_-93+1464delinsCTG	ENSP00000443907.1:n.-93+1462_-93+1464delinsCTG
NM_001099282.1:c.-216+559_-216+561delinsCTG	NP_001092752.1:n.-216+559_-216+561delinsCTG
NM_001099283.1:c.-93+1462_-93+1464delinsCTG	NP_001092753.1:n.-93+1462_-93+1464delinsCTG
NM_001099284.1:c.-216+1462_-216+1464delinsCTG	NP_001092754.1:n.-216+1462_-216+1464delinsCTG
XM_005271828.1:c.-216+559_-216+561delinsCTG	XP_005271885.1:n.-216+559_-216+561delinsCTG
XM_005271829.1:c.-216+1393_-216+1395delinsCTG	XP_005271886.1:n.-216+1393_-216+1395delinsCTG
XM_005271831.1:c.-93+1393_-93+1395delinsCTG	XP_005271888.1:n.-93+1393_-93+1395delinsCTG
XM_006718002.1:c.-93+559_-93+561delinsCTG	XP_006718065.1:n.-93+559_-93+561delinsCTG
XM_006718003.2:c.-93+960_-93+962delinsCTG	XP_006718066.1:n.-93+960_-93+962delinsCTG
XM_011540233.1:c.-94+559_-94+561delinsCTG	XP_011538535.1:n.-94+559_-94+561delinsCTG
XM_011540234.1:c.-94+1462_-94+1464delinsCTG	XP_011538536.1:n.-94+1462_-94+1464delinsCTG
XM_011540235.1:c.-94+1393_-94+1395delinsCTG	XP_011538537.1:n.-94+1393_-94+1395delinsCTG
XM_011540236.1:c.-94+960_-94+962delinsCTG	XP_011538538.1:n.-94+960_-94+962delinsCTG
NM_001324347.1:c.-93+559_-93+561delinsCTG	NP_001311276.1:n.-93+559_-93+561delinsCTG
NM_001324348.1:c.-93+1393_-93+1395delinsCTG	NP_001311277.1:n.-93+1393_-93+1395delinsCTG
NM_001324349.1:c.-216+559_-216+561delinsCTG	NP_001311278.1:n.-216+559_-216+561delinsCTG
NM_001324350.1:c.-93+559_-93+561delinsCTG	NP_001311279.1:n.-93+559_-93+561delinsCTG
NM_001324351.1:c.-216+1393_-216+1395delinsCTG	NP_001311280.1:n.-216+1393_-216+1395delinsCTG
NM_001324352.1:c.-94+559_-94+561delinsCTG	NP_001311281.1:n.-94+559_-94+561delinsCTG
NM_001324353.1:c.15+559_15+561delinsCTG	NP_001311282.1:n.15+559_15+561delinsCTG
XM_006718003.3:c.-93+960_-93+962delinsCTG	XP_006718066.1:n.-93+960_-93+962delinsCTG
XM_011540232.3:c.-2688_-2686delinsCTG	XP_011538534.1:n.-2688_-2686delinsCTG
XM_011540234.2:c.-94+1462_-94+1464delinsCTG	XP_011538536.1:n.-94+1462_-94+1464delinsCTG
XM_011540235.2:c.-94+1393_-94+1395delinsCTG	XP_011538537.1:n.-94+1393_-94+1395delinsCTG
XM_011540236.2:c.-94+960_-94+962delinsCTG	XP_011538538.1:n.-94+960_-94+962delinsCTG
XM_017016740.1:c.-94+559_-94+561delinsCTG	XP_016872229.1:n.-94+559_-94+561delinsCTG
NM_001099282.2:c.-216+559_-216+561delinsCTG MANE Select	NP_001092752.1:n.-216+559_-216+561delinsCTG
NM_001324347.2:c.-93+559_-93+561delinsCTG	NP_001311276.1:n.-93+559_-93+561delinsCTG
NM_001324348.2:c.-93+1393_-93+1395delinsCTG	NP_001311277.1:n.-93+1393_-93+1395delinsCTG
NM_001324349.2:c.-216+559_-216+561delinsCTG	NP_001311278.1:n.-216+559_-216+561delinsCTG
NM_001324350.2:c.-93+559_-93+561delinsCTG	NP_001311279.1:n.-93+559_-93+561delinsCTG
NM_001324351.2:c.-216+1393_-216+1395delinsCTG	NP_001311280.1:n.-216+1393_-216+1395delinsCTG
NM_001324352.2:c.-94+559_-94+561delinsCTG	NP_001311281.1:n.-94+559_-94+561delinsCTG
NM_001324353.2:c.15+559_15+561delinsCTG	NP_001311282.1:n.15+559_15+561delinsCTG
NM_001099283.2:c.-93+1462_-93+1464delinsCTG	NP_001092753.1:n.-93+1462_-93+1464delinsCTG
NM_001099284.2:c.-216+1462_-216+1464delinsCTG	NP_001092754.1:n.-216+1462_-216+1464delinsCTG