Canonical Allele Identifier: CA433709091

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380392C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342961C>T , CM000665.2:g.50342961C>T	GRCh38
NC_000003.11:g.50380392C>T , CM000665.1:g.50380392C>T	GRCh37
NC_000003.10:g.50355396C>T	NCBI36
NG_023270.1:g.2976G>A
NG_042828.1:g.7786G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.657G>A MANE Select	ENSP00000231749.3:p.Leu219=
ENST00000231749.7:c.657G>A	ENSP00000231749.3:p.Leu219=
ENST00000360165.7:c.599+157G>A	ENSP00000353289.3:n.599+157G>A
ENST00000442887.1:c.528G>A	ENSP00000393687.1:p.Leu176=
ENST00000443080.5:c.*409G>A	ENSP00000415661.1:n.*409G>A
ENST00000475688.1:n.208G>A
NM_001308379.1:c.599+157G>A	NP_001295308.1:n.599+157G>A
NM_015896.2:c.657G>A	NP_056980.2:p.Leu219=
NM_015896.3:c.657G>A	NP_056980.2:p.Leu219=
XM_005265216.2:c.420G>A	XP_005265273.1:p.Leu140=
XM_005265216.3:c.420G>A	XP_005265273.1:p.Leu140=
NM_015896.4:c.657G>A MANE Select	NP_056980.2:p.Leu219=
NM_001308379.2:c.599+157G>A	NP_001295308.1:n.599+157G>A