Canonical Allele Identifier: CA1906044924
Gene: ZNF239 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43573040_43573044delinsGAAGA , CM000672.2:g.43573040_43573044delinsGAAGA GRCh38
NC_000010.10:g.44068488_44068492delinsGAAGA , CM000672.1:g.44068488_44068492delinsGAAGA GRCh37
NC_000010.9:g.43388494_43388498delinsGAAGA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374446.7:c.-216+593_-216+597delinsTCTTC MANE Select ENSP00000363569.1:n.-216+593_-216+597deli...
ENST00000374446.6:c.-216+593_-216+597delinsTCTTC ENSP00000363569.1:n.-216+593_-216+597deli...
ENST00000426961.1:c.-216+1496_-216+1500delinsTCTTC ENSP00000398202.1:n.-216+1496_-216+1500de...
ENST00000491188.1:n.58+1496_58+1500delinsTCTTC
ENST00000535642.5:c.-93+1496_-93+1500delinsTCTTC ENSP00000443907.1:n.-93+1496_-93+1500deli...
NM_001099282.1:c.-216+593_-216+597delinsTCTTC NP_001092752.1:n.-216+593_-216+597delinsT...
NM_001099283.1:c.-93+1496_-93+1500delinsTCTTC NP_001092753.1:n.-93+1496_-93+1500delinsT...
NM_001099284.1:c.-216+1496_-216+1500delinsTCTTC NP_001092754.1:n.-216+1496_-216+1500delin...
XM_005271828.1:c.-216+593_-216+597delinsTCTTC XP_005271885.1:n.-216+593_-216+597delinsT...
XM_005271829.1:c.-216+1427_-216+1431delinsTCTTC XP_005271886.1:n.-216+1427_-216+1431delin...
XM_005271831.1:c.-93+1427_-93+1431delinsTCTTC XP_005271888.1:n.-93+1427_-93+1431delinsT...
XM_006718002.1:c.-93+593_-93+597delinsTCTTC XP_006718065.1:n.-93+593_-93+597delinsTCT...
XM_006718003.2:c.-93+994_-93+998delinsTCTTC XP_006718066.1:n.-93+994_-93+998delinsTCT...
XM_011540233.1:c.-94+593_-94+597delinsTCTTC XP_011538535.1:n.-94+593_-94+597delinsTCT...
XM_011540234.1:c.-94+1496_-94+1500delinsTCTTC XP_011538536.1:n.-94+1496_-94+1500delinsT...
XM_011540235.1:c.-94+1427_-94+1431delinsTCTTC XP_011538537.1:n.-94+1427_-94+1431delinsT...
XM_011540236.1:c.-94+994_-94+998delinsTCTTC XP_011538538.1:n.-94+994_-94+998delinsTCT...
NM_001324347.1:c.-93+593_-93+597delinsTCTTC NP_001311276.1:n.-93+593_-93+597delinsTCT...
NM_001324348.1:c.-93+1427_-93+1431delinsTCTTC NP_001311277.1:n.-93+1427_-93+1431delinsT...
NM_001324349.1:c.-216+593_-216+597delinsTCTTC NP_001311278.1:n.-216+593_-216+597delinsT...
NM_001324350.1:c.-93+593_-93+597delinsTCTTC NP_001311279.1:n.-93+593_-93+597delinsTCT...
NM_001324351.1:c.-216+1427_-216+1431delinsTCTTC NP_001311280.1:n.-216+1427_-216+1431delin...
NM_001324352.1:c.-94+593_-94+597delinsTCTTC NP_001311281.1:n.-94+593_-94+597delinsTCT...
NM_001324353.1:c.15+593_15+597delinsTCTTC NP_001311282.1:n.15+593_15+597delinsTCTTC...
XM_006718003.3:c.-93+994_-93+998delinsTCTTC XP_006718066.1:n.-93+994_-93+998delinsTCT...
XM_011540232.3:c.-2654_-2650delinsTCTTC XP_011538534.1:n.-2654_-2650delinsTCTTC
XM_011540234.2:c.-94+1496_-94+1500delinsTCTTC XP_011538536.1:n.-94+1496_-94+1500delinsT...
XM_011540235.2:c.-94+1427_-94+1431delinsTCTTC XP_011538537.1:n.-94+1427_-94+1431delinsT...
XM_011540236.2:c.-94+994_-94+998delinsTCTTC XP_011538538.1:n.-94+994_-94+998delinsTCT...
XM_017016740.1:c.-94+593_-94+597delinsTCTTC XP_016872229.1:n.-94+593_-94+597delinsTCT...
NM_001099282.2:c.-216+593_-216+597delinsTCTTC MANE Select NP_001092752.1:n.-216+593_-216+597delinsT...
NM_001324347.2:c.-93+593_-93+597delinsTCTTC NP_001311276.1:n.-93+593_-93+597delinsTCT...
NM_001324348.2:c.-93+1427_-93+1431delinsTCTTC NP_001311277.1:n.-93+1427_-93+1431delinsT...
NM_001324349.2:c.-216+593_-216+597delinsTCTTC NP_001311278.1:n.-216+593_-216+597delinsT...
NM_001324350.2:c.-93+593_-93+597delinsTCTTC NP_001311279.1:n.-93+593_-93+597delinsTCT...
NM_001324351.2:c.-216+1427_-216+1431delinsTCTTC NP_001311280.1:n.-216+1427_-216+1431delin...
NM_001324352.2:c.-94+593_-94+597delinsTCTTC NP_001311281.1:n.-94+593_-94+597delinsTCT...
NM_001324353.2:c.15+593_15+597delinsTCTTC NP_001311282.1:n.15+593_15+597delinsTCTTC...
NM_001099283.2:c.-93+1496_-93+1500delinsTCTTC NP_001092753.1:n.-93+1496_-93+1500delinsT...
NM_001099284.2:c.-216+1496_-216+1500delinsTCTTC NP_001092754.1:n.-216+1496_-216+1500delin...