Canonical Allele Identifier: CA645524274
Gene: ZMYND10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50343153del , CM000665.2:g.50343153del GRCh38
NC_000003.11:g.50380584del , CM000665.1:g.50380584del GRCh37
NC_000003.10:g.50355588del NCBI36
NG_023270.1:g.2784del
NG_042828.1:g.7594del

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.8:c.564del MANE Select ENSP00000231749.3:p.Ser189GlnfsTer18
ENST00000231749.7:c.564del ENSP00000231749.3:p.Ser189GlnfsTer18
ENST00000360165.7:c.564del ENSP00000353289.3:p.Ser189GlnfsTer25
ENST00000442887.1:c.435del ENSP00000393687.1:p.Ser146GlnfsTer18
ENST00000443080.5:c.*316del ENSP00000415661.1:n.*316del
ENST00000475688.1:n.16del
NM_001308379.1:c.564del NP_001295308.1:p.Ser189GlnfsTer25
NM_015896.2:c.564del NP_056980.2:p.Ser189GlnfsTer18
NM_015896.3:c.564del NP_056980.2:p.Ser189GlnfsTer18
XM_005265216.2:c.327del XP_005265273.1:p.Ser110GlnfsTer18
XM_005265216.3:c.327del XP_005265273.1:p.Ser110GlnfsTer18
NM_015896.4:c.564del MANE Select NP_056980.2:p.Ser189GlnfsTer18
NM_001308379.2:c.564del NP_001295308.1:p.Ser189GlnfsTer25