Canonical Allele Identifier: CA352942343

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1703443381
• gnomAD v3: 3-50343205-T-A
• gnomAD v4: 3-50343205-T-A
• MyVariant Identifiers: chr3:g.50380636T>A (hg19) ; chr3:g.50343205T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343205T>A , CM000665.2:g.50343205T>A	GRCh38
NC_000003.11:g.50380636T>A , CM000665.1:g.50380636T>A	GRCh37
NC_000003.10:g.50355640T>A	NCBI36
NG_023270.1:g.2732A>T
NG_042828.1:g.7542A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.512A>T MANE Select	ENSP00000231749.3:p.Glu171Val
ENST00000231749.7:c.512A>T	ENSP00000231749.3:p.Glu171Val
ENST00000360165.7:c.512A>T	ENSP00000353289.3:p.Glu171Val
ENST00000442887.1:c.383A>T	ENSP00000393687.1:p.Glu128Val
ENST00000443080.5:c.*264A>T	ENSP00000415661.1:n.*264A>T
ENST00000478269.5:n.597A>T
NM_001308379.1:c.512A>T	NP_001295308.1:p.Glu171Val
NM_015896.2:c.512A>T	NP_056980.2:p.Glu171Val
NM_015896.3:c.512A>T	NP_056980.2:p.Glu171Val
XM_005265216.2:c.275A>T	XP_005265273.1:p.Glu92Val
XM_005265216.3:c.275A>T	XP_005265273.1:p.Glu92Val
NM_015896.4:c.512A>T MANE Select	NP_056980.2:p.Glu171Val
NM_001308379.2:c.512A>T	NP_001295308.1:p.Glu171Val