Canonical Allele Identifier: CA665373554

Gene: ZNF239

Linked Data

• dbSNP Id: rs1458644402
• MyVariant Identifiers: chr10:g.44068489_44068492del (hg19) ; chr10:g.43573041_43573044del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43573041_43573044del , CM000672.2:g.43573041_43573044del	GRCh38
NC_000010.10:g.44068489_44068492del , CM000672.1:g.44068489_44068492del	GRCh37
NC_000010.9:g.43388495_43388498del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000374446.7:c.-216+593_-216+596del MANE Select	ENSP00000363569.1:n.-216+593_-216+596del
ENST00000374446.6:c.-216+593_-216+596del	ENSP00000363569.1:n.-216+593_-216+596del
ENST00000426961.1:c.-216+1496_-216+1499del	ENSP00000398202.1:n.-216+1496_-216+1499de...
ENST00000491188.1:n.58+1496_58+1499del
ENST00000535642.5:c.-93+1496_-93+1499del	ENSP00000443907.1:n.-93+1496_-93+1499del
NM_001099282.1:c.-216+593_-216+596del	NP_001092752.1:n.-216+593_-216+596del
NM_001099283.1:c.-93+1496_-93+1499del	NP_001092753.1:n.-93+1496_-93+1499del
NM_001099284.1:c.-216+1496_-216+1499del	NP_001092754.1:n.-216+1496_-216+1499del
XM_005271828.1:c.-216+593_-216+596del	XP_005271885.1:n.-216+593_-216+596del
XM_005271829.1:c.-216+1427_-216+1430del	XP_005271886.1:n.-216+1427_-216+1430del
XM_005271831.1:c.-93+1427_-93+1430del	XP_005271888.1:n.-93+1427_-93+1430del
XM_006718002.1:c.-93+593_-93+596del	XP_006718065.1:n.-93+593_-93+596del
XM_006718003.2:c.-93+994_-93+997del	XP_006718066.1:n.-93+994_-93+997del
XM_011540233.1:c.-94+593_-94+596del	XP_011538535.1:n.-94+593_-94+596del
XM_011540234.1:c.-94+1496_-94+1499del	XP_011538536.1:n.-94+1496_-94+1499del
XM_011540235.1:c.-94+1427_-94+1430del	XP_011538537.1:n.-94+1427_-94+1430del
XM_011540236.1:c.-94+994_-94+997del	XP_011538538.1:n.-94+994_-94+997del
NM_001324347.1:c.-93+593_-93+596del	NP_001311276.1:n.-93+593_-93+596del
NM_001324348.1:c.-93+1427_-93+1430del	NP_001311277.1:n.-93+1427_-93+1430del
NM_001324349.1:c.-216+593_-216+596del	NP_001311278.1:n.-216+593_-216+596del
NM_001324350.1:c.-93+593_-93+596del	NP_001311279.1:n.-93+593_-93+596del
NM_001324351.1:c.-216+1427_-216+1430del	NP_001311280.1:n.-216+1427_-216+1430del
NM_001324352.1:c.-94+593_-94+596del	NP_001311281.1:n.-94+593_-94+596del
NM_001324353.1:c.15+593_15+596del	NP_001311282.1:n.15+593_15+596del
XM_006718003.3:c.-93+994_-93+997del	XP_006718066.1:n.-93+994_-93+997del
XM_011540232.3:c.-2654_-2651del	XP_011538534.1:n.-2654_-2651del
XM_011540234.2:c.-94+1496_-94+1499del	XP_011538536.1:n.-94+1496_-94+1499del
XM_011540235.2:c.-94+1427_-94+1430del	XP_011538537.1:n.-94+1427_-94+1430del
XM_011540236.2:c.-94+994_-94+997del	XP_011538538.1:n.-94+994_-94+997del
XM_017016740.1:c.-94+593_-94+596del	XP_016872229.1:n.-94+593_-94+596del
NM_001099282.2:c.-216+593_-216+596del MANE Select	NP_001092752.1:n.-216+593_-216+596del
NM_001324347.2:c.-93+593_-93+596del	NP_001311276.1:n.-93+593_-93+596del
NM_001324348.2:c.-93+1427_-93+1430del	NP_001311277.1:n.-93+1427_-93+1430del
NM_001324349.2:c.-216+593_-216+596del	NP_001311278.1:n.-216+593_-216+596del
NM_001324350.2:c.-93+593_-93+596del	NP_001311279.1:n.-93+593_-93+596del
NM_001324351.2:c.-216+1427_-216+1430del	NP_001311280.1:n.-216+1427_-216+1430del
NM_001324352.2:c.-94+593_-94+596del	NP_001311281.1:n.-94+593_-94+596del
NM_001324353.2:c.15+593_15+596del	NP_001311282.1:n.15+593_15+596del
NM_001099283.2:c.-93+1496_-93+1499del	NP_001092753.1:n.-93+1496_-93+1499del
NM_001099284.2:c.-216+1496_-216+1499del	NP_001092754.1:n.-216+1496_-216+1499del