Canonical Allele Identifier: CA2665843130

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50343212-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343214del , CM000665.2:g.50343214del	GRCh38
NC_000003.11:g.50380645del , CM000665.1:g.50380645del	GRCh37
NC_000003.10:g.50355649del	NCBI36
NG_023270.1:g.2724del
NG_042828.1:g.7534del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.511-7del MANE Select	ENSP00000231749.3:n.511-7del
ENST00000231749.7:c.511-7del	ENSP00000231749.3:n.511-7del
ENST00000360165.7:c.511-7del	ENSP00000353289.3:n.511-7del
ENST00000442887.1:c.382-7del	ENSP00000393687.1:n.382-7del
ENST00000443080.5:c.*263-7del	ENSP00000415661.1:n.*263-7del
ENST00000478269.5:n.589del
NM_001308379.1:c.511-7del	NP_001295308.1:n.511-7del
NM_015896.2:c.511-7del	NP_056980.2:n.511-7del
NM_015896.3:c.511-7del	NP_056980.2:n.511-7del
XM_005265216.2:c.274-7del	XP_005265273.1:n.274-7del
XM_005265216.3:c.274-7del	XP_005265273.1:n.274-7del
NM_015896.4:c.511-7del MANE Select	NP_056980.2:n.511-7del
NM_001308379.2:c.511-7del	NP_001295308.1:n.511-7del