Canonical Allele Identifier: CA1363908874
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345677_50345688delinsAGGACAGTTGCG , CM000665.2:g.50345677_50345688delinsAGGACAGTTGCG GRCh38
NC_000003.11:g.50383108_50383119delinsAGGACAGTTGCG , CM000665.1:g.50383108_50383119delinsAGGACAGTTGCG GRCh37
NC_000003.10:g.50358112_50358123delinsAGGACAGTTGCG NCBI36
NG_023270.1:g.249_260delinsCGCAACTGTCCT
NG_042828.1:g.5059_5070delinsCGCAACTGTCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.8:c.-109_-98delinsCGCAACTGTCCT MANE Select ENSP00000231749.3:n.-109_-98delinsCGCAACTGTCCT
ENST00000231749.7:c.-109_-98delinsCGCAACTGTCCT ENSP00000231749.3:n.-109_-98delinsCGCAACTGTCCT
ENST00000360165.7:c.-109_-98delinsCGCAACTGTCCT ENSP00000353289.3:n.-109_-98delinsCGCAACTGTCCT
ENST00000431869.1:c.-109_-98delinsCGCAACTGTCCT ENSP00000391545.1:n.-109_-98delinsCGCAACTGTCCT
ENST00000442887.1:c.-191_-180delinsCGCAACTGTCCT ENSP00000393687.1:n.-191_-180delinsCGCAACTGTCCT
NM_001308379.1:c.-109_-98delinsCGCAACTGTCCT NP_001295308.1:n.-109_-98delinsCGCAACTGTCCT
NM_015896.2:c.-109_-98delinsCGCAACTGTCCT NP_056980.2:n.-109_-98delinsCGCAACTGTCCT
NM_015896.3:c.-109_-98delinsCGCAACTGTCCT NP_056980.2:n.-109_-98delinsCGCAACTGTCCT
XM_005265216.2:c.-237_-226delinsCGCAACTGTCCT XP_005265273.1:n.-237_-226delinsCGCAACTGTCCT
XM_005265216.3:c.-237_-226delinsCGCAACTGTCCT XP_005265273.1:n.-237_-226delinsCGCAACTGTCCT
NM_015896.4:c.-109_-98delinsCGCAACTGTCCT MANE Select NP_056980.2:n.-109_-98delinsCGCAACTGTCCT
NM_001308379.2:c.-109_-98delinsCGCAACTGTCCT NP_001295308.1:n.-109_-98delinsCGCAACTGTCCT