Canonical Allele Identifier: CA2721759511
Gene: ZNF239 HGNC NCBI

Linked Data

dbSNP Id: rs2132317279

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43573097C>G , CM000672.2:g.43573097C>G GRCh38
NC_000010.10:g.44068545C>G , CM000672.1:g.44068545C>G GRCh37
NC_000010.9:g.43388551C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000374446.7:c.-216+540G>C MANE Select ENSP00000363569.1:n.-216+540G>C
ENST00000374446.6:c.-216+540G>C ENSP00000363569.1:n.-216+540G>C
ENST00000426961.1:c.-216+1443G>C ENSP00000398202.1:n.-216+1443G>C
ENST00000491188.1:n.58+1443G>C
ENST00000535642.5:c.-93+1443G>C ENSP00000443907.1:n.-93+1443G>C
NM_001099282.1:c.-216+540G>C NP_001092752.1:n.-216+540G>C
NM_001099283.1:c.-93+1443G>C NP_001092753.1:n.-93+1443G>C
NM_001099284.1:c.-216+1443G>C NP_001092754.1:n.-216+1443G>C
XM_005271828.1:c.-216+540G>C XP_005271885.1:n.-216+540G>C
XM_005271829.1:c.-216+1374G>C XP_005271886.1:n.-216+1374G>C
XM_005271831.1:c.-93+1374G>C XP_005271888.1:n.-93+1374G>C
XM_006718002.1:c.-93+540G>C XP_006718065.1:n.-93+540G>C
XM_006718003.2:c.-93+941G>C XP_006718066.1:n.-93+941G>C
XM_011540233.1:c.-94+540G>C XP_011538535.1:n.-94+540G>C
XM_011540234.1:c.-94+1443G>C XP_011538536.1:n.-94+1443G>C
XM_011540235.1:c.-94+1374G>C XP_011538537.1:n.-94+1374G>C
XM_011540236.1:c.-94+941G>C XP_011538538.1:n.-94+941G>C
NM_001324347.1:c.-93+540G>C NP_001311276.1:n.-93+540G>C
NM_001324348.1:c.-93+1374G>C NP_001311277.1:n.-93+1374G>C
NM_001324349.1:c.-216+540G>C NP_001311278.1:n.-216+540G>C
NM_001324350.1:c.-93+540G>C NP_001311279.1:n.-93+540G>C
NM_001324351.1:c.-216+1374G>C NP_001311280.1:n.-216+1374G>C
NM_001324352.1:c.-94+540G>C NP_001311281.1:n.-94+540G>C
NM_001324353.1:c.15+540G>C NP_001311282.1:n.15+540G>C
XM_006718003.3:c.-93+941G>C XP_006718066.1:n.-93+941G>C
XM_011540232.3:c.-2707G>C XP_011538534.1:n.-2707G>C
XM_011540234.2:c.-94+1443G>C XP_011538536.1:n.-94+1443G>C
XM_011540235.2:c.-94+1374G>C XP_011538537.1:n.-94+1374G>C
XM_011540236.2:c.-94+941G>C XP_011538538.1:n.-94+941G>C
XM_017016740.1:c.-94+540G>C XP_016872229.1:n.-94+540G>C
NM_001099282.2:c.-216+540G>C MANE Select NP_001092752.1:n.-216+540G>C
NM_001324347.2:c.-93+540G>C NP_001311276.1:n.-93+540G>C
NM_001324348.2:c.-93+1374G>C NP_001311277.1:n.-93+1374G>C
NM_001324349.2:c.-216+540G>C NP_001311278.1:n.-216+540G>C
NM_001324350.2:c.-93+540G>C NP_001311279.1:n.-93+540G>C
NM_001324351.2:c.-216+1374G>C NP_001311280.1:n.-216+1374G>C
NM_001324352.2:c.-94+540G>C NP_001311281.1:n.-94+540G>C
NM_001324353.2:c.15+540G>C NP_001311282.1:n.15+540G>C
NM_001099283.2:c.-93+1443G>C NP_001092753.1:n.-93+1443G>C
NM_001099284.2:c.-216+1443G>C NP_001092754.1:n.-216+1443G>C