Canonical Allele Identifier: CA433709521

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380620T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343189T>G , CM000665.2:g.50343189T>G	GRCh38
NC_000003.11:g.50380620T>G , CM000665.1:g.50380620T>G	GRCh37
NC_000003.10:g.50355624T>G	NCBI36
NG_023270.1:g.2748A>C
NG_042828.1:g.7558A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.528A>C MANE Select	ENSP00000231749.3:p.Ala176=
ENST00000231749.7:c.528A>C	ENSP00000231749.3:p.Ala176=
ENST00000360165.7:c.528A>C	ENSP00000353289.3:p.Ala176=
ENST00000442887.1:c.399A>C	ENSP00000393687.1:p.Ala133=
ENST00000443080.5:c.*280A>C	ENSP00000415661.1:n.*280A>C
ENST00000478269.5:n.613A>C
NM_001308379.1:c.528A>C	NP_001295308.1:p.Ala176=
NM_015896.2:c.528A>C	NP_056980.2:p.Ala176=
NM_015896.3:c.528A>C	NP_056980.2:p.Ala176=
XM_005265216.2:c.291A>C	XP_005265273.1:p.Ala97=
XM_005265216.3:c.291A>C	XP_005265273.1:p.Ala97=
NM_015896.4:c.528A>C MANE Select	NP_056980.2:p.Ala176=
NM_001308379.2:c.528A>C	NP_001295308.1:p.Ala176=