Canonical Allele Identifier: CA2721759490

Gene: ZNF239

Linked Data

• dbSNP Id: rs2132316512

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43572961_43572962del , CM000672.2:g.43572961_43572962del	GRCh38
NC_000010.10:g.44068409_44068410del , CM000672.1:g.44068409_44068410del	GRCh37
NC_000010.9:g.43388415_43388416del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374446.7:c.-216+680_-216+681del MANE Select	ENSP00000363569.1:n.-216+680_-216+681del
ENST00000374446.6:c.-216+680_-216+681del	ENSP00000363569.1:n.-216+680_-216+681del
ENST00000426961.1:c.-216+1583_-216+1584del	ENSP00000398202.1:n.-216+1583_-216+1584del
ENST00000491188.1:n.58+1583_58+1584del
ENST00000535642.5:c.-93+1583_-93+1584del	ENSP00000443907.1:n.-93+1583_-93+1584del
NM_001099282.1:c.-216+680_-216+681del	NP_001092752.1:n.-216+680_-216+681del
NM_001099283.1:c.-93+1583_-93+1584del	NP_001092753.1:n.-93+1583_-93+1584del
NM_001099284.1:c.-216+1583_-216+1584del	NP_001092754.1:n.-216+1583_-216+1584del
XM_005271828.1:c.-216+680_-216+681del	XP_005271885.1:n.-216+680_-216+681del
XM_005271829.1:c.-216+1514_-216+1515del	XP_005271886.1:n.-216+1514_-216+1515del
XM_005271831.1:c.-93+1514_-93+1515del	XP_005271888.1:n.-93+1514_-93+1515del
XM_006718002.1:c.-93+680_-93+681del	XP_006718065.1:n.-93+680_-93+681del
XM_006718003.2:c.-93+1081_-93+1082del	XP_006718066.1:n.-93+1081_-93+1082del
XM_011540233.1:c.-94+680_-94+681del	XP_011538535.1:n.-94+680_-94+681del
XM_011540234.1:c.-94+1583_-94+1584del	XP_011538536.1:n.-94+1583_-94+1584del
XM_011540235.1:c.-94+1514_-94+1515del	XP_011538537.1:n.-94+1514_-94+1515del
XM_011540236.1:c.-94+1081_-94+1082del	XP_011538538.1:n.-94+1081_-94+1082del
NM_001324347.1:c.-93+680_-93+681del	NP_001311276.1:n.-93+680_-93+681del
NM_001324348.1:c.-93+1514_-93+1515del	NP_001311277.1:n.-93+1514_-93+1515del
NM_001324349.1:c.-216+680_-216+681del	NP_001311278.1:n.-216+680_-216+681del
NM_001324350.1:c.-93+680_-93+681del	NP_001311279.1:n.-93+680_-93+681del
NM_001324351.1:c.-216+1514_-216+1515del	NP_001311280.1:n.-216+1514_-216+1515del
NM_001324352.1:c.-94+680_-94+681del	NP_001311281.1:n.-94+680_-94+681del
NM_001324353.1:c.15+680_15+681del	NP_001311282.1:n.15+680_15+681del
XM_006718003.3:c.-93+1081_-93+1082del	XP_006718066.1:n.-93+1081_-93+1082del
XM_011540232.3:c.-2567_-2566del	XP_011538534.1:n.-2567_-2566del
XM_011540234.2:c.-94+1583_-94+1584del	XP_011538536.1:n.-94+1583_-94+1584del
XM_011540235.2:c.-94+1514_-94+1515del	XP_011538537.1:n.-94+1514_-94+1515del
XM_011540236.2:c.-94+1081_-94+1082del	XP_011538538.1:n.-94+1081_-94+1082del
XM_017016740.1:c.-94+680_-94+681del	XP_016872229.1:n.-94+680_-94+681del
NM_001099282.2:c.-216+680_-216+681del MANE Select	NP_001092752.1:n.-216+680_-216+681del
NM_001324347.2:c.-93+680_-93+681del	NP_001311276.1:n.-93+680_-93+681del
NM_001324348.2:c.-93+1514_-93+1515del	NP_001311277.1:n.-93+1514_-93+1515del
NM_001324349.2:c.-216+680_-216+681del	NP_001311278.1:n.-216+680_-216+681del
NM_001324350.2:c.-93+680_-93+681del	NP_001311279.1:n.-93+680_-93+681del
NM_001324351.2:c.-216+1514_-216+1515del	NP_001311280.1:n.-216+1514_-216+1515del
NM_001324352.2:c.-94+680_-94+681del	NP_001311281.1:n.-94+680_-94+681del
NM_001324353.2:c.15+680_15+681del	NP_001311282.1:n.15+680_15+681del
NM_001099283.2:c.-93+1583_-93+1584del	NP_001092753.1:n.-93+1583_-93+1584del
NM_001099284.2:c.-216+1583_-216+1584del	NP_001092754.1:n.-216+1583_-216+1584del