Canonical Allele Identifier: CA1906044919
Gene: ZNF239 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43573038_43573039delinsTG , CM000672.2:g.43573038_43573039delinsTG GRCh38
NC_000010.10:g.44068486_44068487delinsTG , CM000672.1:g.44068486_44068487delinsTG GRCh37
NC_000010.9:g.43388492_43388493delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374446.7:c.-216+598_-216+599delinsCA MANE Select ENSP00000363569.1:n.-216+598_-216+599deli...
ENST00000374446.6:c.-216+598_-216+599delinsCA ENSP00000363569.1:n.-216+598_-216+599deli...
ENST00000426961.1:c.-216+1501_-216+1502delinsCA ENSP00000398202.1:n.-216+1501_-216+1502de...
ENST00000491188.1:n.58+1501_58+1502delinsCA
ENST00000535642.5:c.-93+1501_-93+1502delinsCA ENSP00000443907.1:n.-93+1501_-93+1502deli...
NM_001099282.1:c.-216+598_-216+599delinsCA NP_001092752.1:n.-216+598_-216+599delinsC...
NM_001099283.1:c.-93+1501_-93+1502delinsCA NP_001092753.1:n.-93+1501_-93+1502delinsC...
NM_001099284.1:c.-216+1501_-216+1502delinsCA NP_001092754.1:n.-216+1501_-216+1502delin...
XM_005271828.1:c.-216+598_-216+599delinsCA XP_005271885.1:n.-216+598_-216+599delinsC...
XM_005271829.1:c.-216+1432_-216+1433delinsCA XP_005271886.1:n.-216+1432_-216+1433delin...
XM_005271831.1:c.-93+1432_-93+1433delinsCA XP_005271888.1:n.-93+1432_-93+1433delinsC...
XM_006718002.1:c.-93+598_-93+599delinsCA XP_006718065.1:n.-93+598_-93+599delinsCA
XM_006718003.2:c.-93+999_-93+1000delinsCA XP_006718066.1:n.-93+999_-93+1000delinsCA...
XM_011540233.1:c.-94+598_-94+599delinsCA XP_011538535.1:n.-94+598_-94+599delinsCA
XM_011540234.1:c.-94+1501_-94+1502delinsCA XP_011538536.1:n.-94+1501_-94+1502delinsC...
XM_011540235.1:c.-94+1432_-94+1433delinsCA XP_011538537.1:n.-94+1432_-94+1433delinsC...
XM_011540236.1:c.-94+999_-94+1000delinsCA XP_011538538.1:n.-94+999_-94+1000delinsCA...
NM_001324347.1:c.-93+598_-93+599delinsCA NP_001311276.1:n.-93+598_-93+599delinsCA
NM_001324348.1:c.-93+1432_-93+1433delinsCA NP_001311277.1:n.-93+1432_-93+1433delinsC...
NM_001324349.1:c.-216+598_-216+599delinsCA NP_001311278.1:n.-216+598_-216+599delinsC...
NM_001324350.1:c.-93+598_-93+599delinsCA NP_001311279.1:n.-93+598_-93+599delinsCA
NM_001324351.1:c.-216+1432_-216+1433delinsCA NP_001311280.1:n.-216+1432_-216+1433delin...
NM_001324352.1:c.-94+598_-94+599delinsCA NP_001311281.1:n.-94+598_-94+599delinsCA
NM_001324353.1:c.15+598_15+599delinsCA NP_001311282.1:n.15+598_15+599delinsCA
XM_006718003.3:c.-93+999_-93+1000delinsCA XP_006718066.1:n.-93+999_-93+1000delinsCA...
XM_011540232.3:c.-2649_-2648delinsCA XP_011538534.1:n.-2649_-2648delinsCA
XM_011540234.2:c.-94+1501_-94+1502delinsCA XP_011538536.1:n.-94+1501_-94+1502delinsC...
XM_011540235.2:c.-94+1432_-94+1433delinsCA XP_011538537.1:n.-94+1432_-94+1433delinsC...
XM_011540236.2:c.-94+999_-94+1000delinsCA XP_011538538.1:n.-94+999_-94+1000delinsCA...
XM_017016740.1:c.-94+598_-94+599delinsCA XP_016872229.1:n.-94+598_-94+599delinsCA
NM_001099282.2:c.-216+598_-216+599delinsCA MANE Select NP_001092752.1:n.-216+598_-216+599delinsC...
NM_001324347.2:c.-93+598_-93+599delinsCA NP_001311276.1:n.-93+598_-93+599delinsCA
NM_001324348.2:c.-93+1432_-93+1433delinsCA NP_001311277.1:n.-93+1432_-93+1433delinsC...
NM_001324349.2:c.-216+598_-216+599delinsCA NP_001311278.1:n.-216+598_-216+599delinsC...
NM_001324350.2:c.-93+598_-93+599delinsCA NP_001311279.1:n.-93+598_-93+599delinsCA
NM_001324351.2:c.-216+1432_-216+1433delinsCA NP_001311280.1:n.-216+1432_-216+1433delin...
NM_001324352.2:c.-94+598_-94+599delinsCA NP_001311281.1:n.-94+598_-94+599delinsCA
NM_001324353.2:c.15+598_15+599delinsCA NP_001311282.1:n.15+598_15+599delinsCA
NM_001099283.2:c.-93+1501_-93+1502delinsCA NP_001092753.1:n.-93+1501_-93+1502delinsC...
NM_001099284.2:c.-216+1501_-216+1502delinsCA NP_001092754.1:n.-216+1501_-216+1502delin...