Canonical Allele Identifier: CA1363908876
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1703523954

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345682_50345692del , CM000665.2:g.50345682_50345692del GRCh38
NC_000003.11:g.50383113_50383123del , CM000665.1:g.50383113_50383123del GRCh37
NC_000003.10:g.50358117_50358127del NCBI36
NG_023270.1:g.249_259del
NG_042828.1:g.5059_5069del

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.8:c.-109_-99del MANE Select ENSP00000231749.3:n.-109_-99del
ENST00000231749.7:c.-109_-99del ENSP00000231749.3:n.-109_-99del
ENST00000360165.7:c.-109_-99del ENSP00000353289.3:n.-109_-99del
ENST00000431869.1:c.-109_-99del ENSP00000391545.1:n.-109_-99del
ENST00000442887.1:c.-191_-181del ENSP00000393687.1:n.-191_-181del
NM_001308379.1:c.-109_-99del NP_001295308.1:n.-109_-99del
NM_015896.2:c.-109_-99del NP_056980.2:n.-109_-99del
NM_015896.3:c.-109_-99del NP_056980.2:n.-109_-99del
XM_005265216.2:c.-237_-227del XP_005265273.1:n.-237_-227del
XM_005265216.3:c.-237_-227del XP_005265273.1:n.-237_-227del
NM_015896.4:c.-109_-99del MANE Select NP_056980.2:n.-109_-99del
NM_001308379.2:c.-109_-99del NP_001295308.1:n.-109_-99del