Canonical Allele Identifier: CA1363903155
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50343008_50343012delinsTGAGA , CM000665.2:g.50343008_50343012delinsTGAGA GRCh38
NC_000003.11:g.50380439_50380443delinsTGAGA , CM000665.1:g.50380439_50380443delinsTGAGA GRCh37
NC_000003.10:g.50355443_50355447delinsTGAGA NCBI36
NG_023270.1:g.2925_2929delinsTCTCA
NG_042828.1:g.7735_7739delinsTCTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.8:c.606_610delinsTCTCA MANE Select ENSP00000231749.3:p.Ser202=
ENST00000231749.7:c.606_610delinsTCTCA ENSP00000231749.3:p.Ser202=
ENST00000360165.7:c.599+106_599+110delinsTCTCA ENSP00000353289.3:n.599+106_599+110delinsTCTCA
ENST00000442887.1:c.477_481delinsTCTCA ENSP00000393687.1:p.Ser159=
ENST00000443080.5:c.*358_*362delinsTCTCA ENSP00000415661.1:n.*358_*362delinsTCTCA
ENST00000475688.1:n.157_161delinsTCTCA
NM_001308379.1:c.599+106_599+110delinsTCTCA NP_001295308.1:n.599+106_599+110delinsTCTCA
NM_015896.2:c.606_610delinsTCTCA NP_056980.2:p.Ser202=
NM_015896.3:c.606_610delinsTCTCA NP_056980.2:p.Ser202=
XM_005265216.2:c.369_373delinsTCTCA XP_005265273.1:p.Ser123=
XM_005265216.3:c.369_373delinsTCTCA XP_005265273.1:p.Ser123=
NM_015896.4:c.606_610delinsTCTCA MANE Select NP_056980.2:p.Ser202=
NM_001308379.2:c.599+106_599+110delinsTCTCA NP_001295308.1:n.599+106_599+110delinsTCTCA