Canonical Allele Identifier: CA1363908754
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345445A= , CM000665.2:g.50345445A= GRCh38
NC_000003.11:g.50382876A= , CM000665.1:g.50382876A= GRCh37
NC_000003.10:g.50357880A= NCBI36
NG_023270.1:g.492T=
NG_042828.1:g.5302T=

Transcript Alleles

HGVS Amino-acid change
ENST00000231749.8:c.92+43T= MANE Select ENSP00000231749.3:n.92+43T=
ENST00000231749.7:c.92+43T= ENSP00000231749.3:n.92+43T=
ENST00000360165.7:c.92+43T= ENSP00000353289.3:n.92+43T=
ENST00000431869.1:c.92+43T= ENSP00000391545.1:n.92+43T=
ENST00000442887.1:c.-38+90T= ENSP00000393687.1:n.-38+90T=
ENST00000443080.5:c.92+43T= ENSP00000415661.1:n.92+43T=
ENST00000468182.1:n.194+43T=
NM_001308379.1:c.92+43T= NP_001295308.1:n.92+43T=
NM_015896.2:c.92+43T= NP_056980.2:n.92+43T=
NM_015896.3:c.92+43T= NP_056980.2:n.92+43T=
XM_005265216.2:c.-37+43T= XP_005265273.1:n.-37+43T=
XM_005265216.3:c.-37+43T= XP_005265273.1:n.-37+43T=
NM_015896.4:c.92+43T= MANE Select NP_056980.2:n.92+43T=
NM_001308379.2:c.92+43T= NP_001295308.1:n.92+43T=