Canonical Allele Identifier: CA1363908814
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345536A= , CM000665.2:g.50345536A= GRCh38
NC_000003.11:g.50382967A= , CM000665.1:g.50382967A= GRCh37
NC_000003.10:g.50357971A= NCBI36
NG_023270.1:g.401T=
NG_042828.1:g.5211T=

Transcript Alleles

HGVS Amino-acid change
ENST00000231749.8:c.44T= MANE Select ENSP00000231749.3:p.Leu15=
ENST00000231749.7:c.44T= ENSP00000231749.3:p.Leu15=
ENST00000360165.7:c.44T= ENSP00000353289.3:p.Leu15=
ENST00000431869.1:c.44T= ENSP00000391545.1:p.Leu15=
ENST00000442887.1:c.-39T= ENSP00000393687.1:n.-39T=
ENST00000443080.5:c.44T= ENSP00000415661.1:p.Leu15=
ENST00000468182.1:n.146T=
NM_001308379.1:c.44T= NP_001295308.1:p.Leu15=
NM_015896.2:c.44T= NP_056980.2:p.Leu15=
NM_015896.3:c.44T= NP_056980.2:p.Leu15=
XM_005265216.2:c.-85T= XP_005265273.1:n.-85T=
XM_005265216.3:c.-85T= XP_005265273.1:n.-85T=
NM_015896.4:c.44T= MANE Select NP_056980.2:p.Leu15=
NM_001308379.2:c.44T= NP_001295308.1:p.Leu15=