Canonical Allele Identifier: CA1363903177

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343029_50343040delinsGGACGTTGTGAA , CM000665.2:g.50343029_50343040delinsGGACGTTGTGAA	GRCh38
NC_000003.11:g.50380460_50380471delinsGGACGTTGTGAA , CM000665.1:g.50380460_50380471delinsGGACGTTGTGAA	GRCh37
NC_000003.10:g.50355464_50355475delinsGGACGTTGTGAA	NCBI36
NG_023270.1:g.2897_2908delinsTTCACAACGTCC
NG_042828.1:g.7707_7718delinsTTCACAACGTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.600-22_600-11delinsTTCACAACGTCC MANE Select	ENSP00000231749.3:n.600-22_600-11delinsTTCACAACGTCC
ENST00000231749.7:c.600-22_600-11delinsTTCACAACGTCC	ENSP00000231749.3:n.600-22_600-11delinsTTCACAACGTCC
ENST00000360165.7:c.599+78_599+89delinsTTCACAACGTCC	ENSP00000353289.3:n.599+78_599+89delinsTTCACAACGTCC
ENST00000442887.1:c.471-22_471-11delinsTTCACAACGTCC	ENSP00000393687.1:n.471-22_471-11delinsTTCACAACGTCC
ENST00000443080.5:c.*352-22_*352-11delinsTTCACAACGTCC	ENSP00000415661.1:n.*352-22_*352-11delinsTTCACAACGTCC
ENST00000475688.1:n.129_140delinsTTCACAACGTCC
NM_001308379.1:c.599+78_599+89delinsTTCACAACGTCC	NP_001295308.1:n.599+78_599+89delinsTTCACAACGTCC
NM_015896.2:c.600-22_600-11delinsTTCACAACGTCC	NP_056980.2:n.600-22_600-11delinsTTCACAACGTCC
NM_015896.3:c.600-22_600-11delinsTTCACAACGTCC	NP_056980.2:n.600-22_600-11delinsTTCACAACGTCC
XM_005265216.2:c.363-22_363-11delinsTTCACAACGTCC	XP_005265273.1:n.363-22_363-11delinsTTCACAACGTCC
XM_005265216.3:c.363-22_363-11delinsTTCACAACGTCC	XP_005265273.1:n.363-22_363-11delinsTTCACAACGTCC
NM_015896.4:c.600-22_600-11delinsTTCACAACGTCC MANE Select	NP_056980.2:n.600-22_600-11delinsTTCACAACGTCC
NM_001308379.2:c.599+78_599+89delinsTTCACAACGTCC	NP_001295308.1:n.599+78_599+89delinsTTCACAACGTCC