Canonical Allele Identifier: CA2665848460

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50345660-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345661del , CM000665.2:g.50345661del	GRCh38
NC_000003.11:g.50383092del , CM000665.1:g.50383092del	GRCh37
NC_000003.10:g.50358096del	NCBI36
NG_023270.1:g.276del
NG_042828.1:g.5086del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-82del MANE Select	ENSP00000231749.3:n.-82del
ENST00000231749.7:c.-82del	ENSP00000231749.3:n.-82del
ENST00000360165.7:c.-82del	ENSP00000353289.3:n.-82del
ENST00000431869.1:c.-82del	ENSP00000391545.1:n.-82del
ENST00000442887.1:c.-164del	ENSP00000393687.1:n.-164del
ENST00000443080.5:c.-82del	ENSP00000415661.1:n.-82del
ENST00000468182.1:n.21del
NM_001308379.1:c.-82del	NP_001295308.1:n.-82del
NM_015896.2:c.-82del	NP_056980.2:n.-82del
NM_015896.3:c.-82del	NP_056980.2:n.-82del
XM_005265216.2:c.-210del	XP_005265273.1:n.-210del
XM_005265216.3:c.-210del	XP_005265273.1:n.-210del
NM_015896.4:c.-82del MANE Select	NP_056980.2:n.-82del
NM_001308379.2:c.-82del	NP_001295308.1:n.-82del