Canonical Allele Identifier: CA2838359418
Gene: ZNF596 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.239001_239002insC , CM000670.2:g.239001_239002insC GRCh38
NC_000008.10:g.189001_189002insC , CM000670.1:g.189001_189002insC GRCh37
NC_000008.9:g.179001_179002insC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398612.3:c.-72-1823_-72-1822insC MANE Select ENSP00000381613.1:n.-72-1823_-72-1822insC
ENST00000640035.1:c.-72-1823_-72-1822insC ENSP00000491031.1:n.-72-1823_-72-1822insC
ENST00000308811.8:c.-72-1823_-72-1822insC ENSP00000310033.4:n.-72-1823_-72-1822insC
ENST00000320552.6:c.-72-1823_-72-1822insC ENSP00000318719.3:n.-72-1823_-72-1822insC
ENST00000398612.2:c.-72-1823_-72-1822insC ENSP00000381613.1:n.-72-1823_-72-1822insC
ENST00000518320.6:c.-146-1823_-146-1822insC ENSP00000476799.1:n.-146-1823_-146-1822insC
ENST00000518414.5:c.-72-1823_-72-1822insC ENSP00000430552.1:n.-72-1823_-72-1822insC
ENST00000521145.5:c.-72-1823_-72-1822insC ENSP00000429671.1:n.-72-1823_-72-1822insC
ENST00000521238.2:n.465-1823_465-1822insC
ENST00000521270.5:c.-267-1301_-267-1300insC ENSP00000429386.1:n.-267-1301_-267-1300insC
ENST00000522866.5:c.-72-1823_-72-1822insC ENSP00000477126.1:n.-72-1823_-72-1822insC
ENST00000523162.5:c.-72-1823_-72-1822insC ENSP00000430650.1:n.-72-1823_-72-1822insC
ENST00000523418.5:n.233-1823_233-1822insC
NM_001042415.2:c.-72-1823_-72-1822insC NP_001035880.1:n.-72-1823_-72-1822insC
NM_001042416.2:c.-72-1823_-72-1822insC NP_001035881.1:n.-72-1823_-72-1822insC
NM_001287254.1:c.-72-1823_-72-1822insC NP_001274183.1:n.-72-1823_-72-1822insC
NM_001287255.1:c.-72-1823_-72-1822insC NP_001274184.1:n.-72-1823_-72-1822insC
NM_001287256.1:c.-72-1823_-72-1822insC NP_001274185.1:n.-72-1823_-72-1822insC
NM_001287399.1:c.-469-1823_-469-1822insC NP_001274328.1:n.-469-1823_-469-1822insC
NM_173539.3:c.-72-1823_-72-1822insC NP_775810.2:n.-72-1823_-72-1822insC
XM_011534742.1:c.-1568_-1567insC XP_011533044.1:n.-1568_-1567insC
XM_011534743.1:c.-146-1823_-146-1822insC XP_011533045.1:n.-146-1823_-146-1822insC
XM_011534744.1:c.-146-1823_-146-1822insC XP_011533046.1:n.-146-1823_-146-1822insC
XM_017013166.1:c.-1895_-1894insC XP_016868655.1:n.-1895_-1894insC
NM_001042416.3:c.-72-1823_-72-1822insC MANE Select NP_001035881.1:n.-72-1823_-72-1822insC
NM_001042415.3:c.-72-1823_-72-1822insC NP_001035880.1:n.-72-1823_-72-1822insC
NM_001287254.2:c.-72-1823_-72-1822insC NP_001274183.1:n.-72-1823_-72-1822insC