Canonical Allele Identifier: CA433709155

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380413T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342982T>C , CM000665.2:g.50342982T>C	GRCh38
NC_000003.11:g.50380413T>C , CM000665.1:g.50380413T>C	GRCh37
NC_000003.10:g.50355417T>C	NCBI36
NG_023270.1:g.2955A>G
NG_042828.1:g.7765A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.636A>G MANE Select	ENSP00000231749.3:p.Thr212=
ENST00000231749.7:c.636A>G	ENSP00000231749.3:p.Thr212=
ENST00000360165.7:c.599+136A>G	ENSP00000353289.3:n.599+136A>G
ENST00000442887.1:c.507A>G	ENSP00000393687.1:p.Thr169=
ENST00000443080.5:c.*388A>G	ENSP00000415661.1:n.*388A>G
ENST00000475688.1:n.187A>G
NM_001308379.1:c.599+136A>G	NP_001295308.1:n.599+136A>G
NM_015896.2:c.636A>G	NP_056980.2:p.Thr212=
NM_015896.3:c.636A>G	NP_056980.2:p.Thr212=
XM_005265216.2:c.399A>G	XP_005265273.1:p.Thr133=
XM_005265216.3:c.399A>G	XP_005265273.1:p.Thr133=
NM_015896.4:c.636A>G MANE Select	NP_056980.2:p.Thr212=
NM_001308379.2:c.599+136A>G	NP_001295308.1:n.599+136A>G