Canonical Allele Identifier: CA352941959

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50343004-G-T
• MyVariant Identifiers: chr3:g.50380435G>T (hg19) ; chr3:g.50343004G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343004G>T , CM000665.2:g.50343004G>T	GRCh38
NC_000003.11:g.50380435G>T , CM000665.1:g.50380435G>T	GRCh37
NC_000003.10:g.50355439G>T	NCBI36
NG_023270.1:g.2933C>A
NG_042828.1:g.7743C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.614C>A MANE Select	ENSP00000231749.3:p.Thr205Asn
ENST00000231749.7:c.614C>A	ENSP00000231749.3:p.Thr205Asn
ENST00000360165.7:c.599+114C>A	ENSP00000353289.3:n.599+114C>A
ENST00000442887.1:c.485C>A	ENSP00000393687.1:p.Thr162Asn
ENST00000443080.5:c.*366C>A	ENSP00000415661.1:n.*366C>A
ENST00000475688.1:n.165C>A
NM_001308379.1:c.599+114C>A	NP_001295308.1:n.599+114C>A
NM_015896.2:c.614C>A	NP_056980.2:p.Thr205Asn
NM_015896.3:c.614C>A	NP_056980.2:p.Thr205Asn
XM_005265216.2:c.377C>A	XP_005265273.1:p.Thr126Asn
XM_005265216.3:c.377C>A	XP_005265273.1:p.Thr126Asn
NM_015896.4:c.614C>A MANE Select	NP_056980.2:p.Thr205Asn
NM_001308379.2:c.599+114C>A	NP_001295308.1:n.599+114C>A