Canonical Allele Identifier: CA2665847810

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50345310-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345311del , CM000665.2:g.50345311del	GRCh38
NC_000003.11:g.50382742del , CM000665.1:g.50382742del	GRCh37
NC_000003.10:g.50357746del	NCBI36
NG_023270.1:g.626del
NG_042828.1:g.5436del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.93-79del MANE Select	ENSP00000231749.3:n.93-79del
ENST00000231749.7:c.93-79del	ENSP00000231749.3:n.93-79del
ENST00000360165.7:c.93-79del	ENSP00000353289.3:n.93-79del
ENST00000431869.1:c.93-75del	ENSP00000391545.1:n.93-75del
ENST00000442887.1:c.-37-79del	ENSP00000393687.1:n.-37-79del
ENST00000443080.5:c.93-75del	ENSP00000415661.1:n.93-75del
ENST00000468182.1:n.195-79del
NM_001308379.1:c.93-79del	NP_001295308.1:n.93-79del
NM_015896.2:c.93-79del	NP_056980.2:n.93-79del
NM_015896.3:c.93-79del	NP_056980.2:n.93-79del
XM_005265216.2:c.-37+177del	XP_005265273.1:n.-37+177del
XM_005265216.3:c.-37+177del	XP_005265273.1:n.-37+177del
NM_015896.4:c.93-79del MANE Select	NP_056980.2:n.93-79del
NM_001308379.2:c.93-79del	NP_001295308.1:n.93-79del