Canonical Allele Identifier: CA2665853747

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50343184-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343185del , CM000665.2:g.50343185del	GRCh38
NC_000003.11:g.50380616del , CM000665.1:g.50380616del	GRCh37
NC_000003.10:g.50355620del	NCBI36
NG_023270.1:g.2752del
NG_042828.1:g.7562del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.532del MANE Select	ENSP00000231749.3:p.Leu178Ter
ENST00000231749.7:c.532del	ENSP00000231749.3:p.Leu178Ter
ENST00000360165.7:c.532del	ENSP00000353289.3:p.Leu178Ter
ENST00000442887.1:c.403del	ENSP00000393687.1:p.Leu135Ter
ENST00000443080.5:c.*284del	ENSP00000415661.1:n.*284del
ENST00000478269.5:n.617del
NM_001308379.1:c.532del	NP_001295308.1:p.Leu178Ter
NM_015896.2:c.532del	NP_056980.2:p.Leu178Ter
NM_015896.3:c.532del	NP_056980.2:p.Leu178Ter
XM_005265216.2:c.295del	XP_005265273.1:p.Leu99Ter
XM_005265216.3:c.295del	XP_005265273.1:p.Leu99Ter
NM_015896.4:c.532del MANE Select	NP_056980.2:p.Leu178Ter
NM_001308379.2:c.532del	NP_001295308.1:p.Leu178Ter