Canonical Allele Identifier: CA1363903312
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50343198C= , CM000665.2:g.50343198C= GRCh38
NC_000003.11:g.50380629C= , CM000665.1:g.50380629C= GRCh37
NC_000003.10:g.50355633C= NCBI36
NG_023270.1:g.2739G=
NG_042828.1:g.7549G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.8:c.519G= MANE Select ENSP00000231749.3:p.Gln173=
ENST00000231749.7:c.519G= ENSP00000231749.3:p.Gln173=
ENST00000360165.7:c.519G= ENSP00000353289.3:p.Gln173=
ENST00000442887.1:c.390G= ENSP00000393687.1:p.Gln130=
ENST00000443080.5:c.*271G= ENSP00000415661.1:n.*271G=
ENST00000478269.5:n.604G=
NM_001308379.1:c.519G= NP_001295308.1:p.Gln173=
NM_015896.2:c.519G= NP_056980.2:p.Gln173=
NM_015896.3:c.519G= NP_056980.2:p.Gln173=
XM_005265216.2:c.282G= XP_005265273.1:p.Gln94=
XM_005265216.3:c.282G= XP_005265273.1:p.Gln94=
NM_015896.4:c.519G= MANE Select NP_056980.2:p.Gln173=
NM_001308379.2:c.519G= NP_001295308.1:p.Gln173=