Canonical Allele Identifier: CA2417198
Community Standard Title: NM_015896.4(ZMYND10):c.485G>A (p.Gly162Glu)
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50343332C>T , CM000665.2:g.50343332C>T GRCh38
NC_000003.11:g.50380763C>T , CM000665.1:g.50380763C>T GRCh37
NC_000003.10:g.50355767C>T NCBI36
NG_023270.1:g.2605G>A
NG_042828.1:g.7415G>A

Transcript Alleles

HGVS Amino-acid Change
NM_015896.4:c.485G>A MANE Select NP_056980.2:p.Gly162Glu
ENST00000231749.8:c.485G>A MANE Select ENSP00000231749.3:p.Gly162Glu
NM_001308379.1:c.485G>A NP_001295308.1:p.Gly162Glu
NM_001308379.2:c.485G>A NP_001295308.1:p.Gly162Glu
NM_015896.2:c.485G>A NP_056980.2:p.Gly162Glu
NM_015896.3:c.485G>A NP_056980.2:p.Gly162Glu
ENST00000231749.7:c.485G>A ENSP00000231749.3:p.Gly162Glu
ENST00000360165.7:c.485G>A ENSP00000353289.3:p.Gly162Glu
ENST00000442887.1:c.356G>A ENSP00000393687.1:p.Gly119Glu
ENST00000443080.5:c.*263-126G>A ENSP00000415661.1:n.*263-126G>A
ENST00000478269.5:n.470G>A
XM_005265216.2:c.248G>A XP_005265273.1:p.Gly83Glu
XM_005265216.3:c.248G>A XP_005265273.1:p.Gly83Glu