Canonical Allele Identifier: CA543053915

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1346790738
• gnomAD v2: 3-50383059-GC-G
• gnomAD v4: 3-50345628-GC-G
• MyVariant Identifiers: chr3:g.50383060del (hg19) ; chr3:g.50345629del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345629del , CM000665.2:g.50345629del	GRCh38
NC_000003.11:g.50383060del , CM000665.1:g.50383060del	GRCh37
NC_000003.10:g.50358064del	NCBI36
NG_023270.1:g.308del
NG_042828.1:g.5118del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-50del MANE Select	ENSP00000231749.3:n.-50del
ENST00000231749.7:c.-50del	ENSP00000231749.3:n.-50del
ENST00000360165.7:c.-50del	ENSP00000353289.3:n.-50del
ENST00000431869.1:c.-50del	ENSP00000391545.1:n.-50del
ENST00000442887.1:c.-132del	ENSP00000393687.1:n.-132del
ENST00000443080.5:c.-50del	ENSP00000415661.1:n.-50del
ENST00000468182.1:n.53del
NM_001308379.1:c.-50del	NP_001295308.1:n.-50del
NM_015896.2:c.-50del	NP_056980.2:n.-50del
NM_015896.3:c.-50del	NP_056980.2:n.-50del
XM_005265216.2:c.-178del	XP_005265273.1:n.-178del
XM_005265216.3:c.-178del	XP_005265273.1:n.-178del
NM_015896.4:c.-50del MANE Select	NP_056980.2:n.-50del
NM_001308379.2:c.-50del	NP_001295308.1:n.-50del