Canonical Allele Identifier: CA2665853743
Gene: ZMYND10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50343134del , CM000665.2:g.50343134del GRCh38
NC_000003.11:g.50380565del , CM000665.1:g.50380565del GRCh37
NC_000003.10:g.50355569del NCBI36
NG_023270.1:g.2803del
NG_042828.1:g.7613del

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.8:c.583del MANE Select ENSP00000231749.3:p.Thr195GlnfsTer12
ENST00000231749.7:c.583del ENSP00000231749.3:p.Thr195GlnfsTer12
ENST00000360165.7:c.583del ENSP00000353289.3:p.Thr195GlnfsTer19
ENST00000442887.1:c.454del ENSP00000393687.1:p.Thr152GlnfsTer12
ENST00000443080.5:c.*335del ENSP00000415661.1:n.*335del
ENST00000475688.1:n.35del
NM_001308379.1:c.583del NP_001295308.1:p.Thr195GlnfsTer19
NM_015896.2:c.583del NP_056980.2:p.Thr195GlnfsTer12
NM_015896.3:c.583del NP_056980.2:p.Thr195GlnfsTer12
XM_005265216.2:c.346del XP_005265273.1:p.Thr116GlnfsTer12
XM_005265216.3:c.346del XP_005265273.1:p.Thr116GlnfsTer12
NM_015896.4:c.583del MANE Select NP_056980.2:p.Thr195GlnfsTer12
NM_001308379.2:c.583del NP_001295308.1:p.Thr195GlnfsTer19