Canonical Allele Identifier: CA1363908707
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345360G= , CM000665.2:g.50345360G= GRCh38
NC_000003.11:g.50382791G= , CM000665.1:g.50382791G= GRCh37
NC_000003.10:g.50357795G= NCBI36
NG_023270.1:g.577C=
NG_042828.1:g.5387C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.8:c.93-128C= MANE Select ENSP00000231749.3:n.93-128C=
ENST00000231749.7:c.93-128C= ENSP00000231749.3:n.93-128C=
ENST00000360165.7:c.93-128C= ENSP00000353289.3:n.93-128C=
ENST00000431869.1:c.93-124C= ENSP00000391545.1:n.93-124C=
ENST00000442887.1:c.-37-128C= ENSP00000393687.1:n.-37-128C=
ENST00000443080.5:c.93-124C= ENSP00000415661.1:n.93-124C=
ENST00000468182.1:n.195-128C=
NM_001308379.1:c.93-128C= NP_001295308.1:n.93-128C=
NM_015896.2:c.93-128C= NP_056980.2:n.93-128C=
NM_015896.3:c.93-128C= NP_056980.2:n.93-128C=
XM_005265216.2:c.-37+128C= XP_005265273.1:n.-37+128C=
XM_005265216.3:c.-37+128C= XP_005265273.1:n.-37+128C=
NM_015896.4:c.93-128C= MANE Select NP_056980.2:n.93-128C=
NM_001308379.2:c.93-128C= NP_001295308.1:n.93-128C=