Canonical Allele Identifier: CA352940242

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342539C>T , CM000665.2:g.50342539C>T	GRCh38
NC_000003.11:g.50379970C>T , CM000665.1:g.50379970C>T	GRCh37
NC_000003.10:g.50354974C>T	NCBI36
NG_023270.1:g.3398G>A
NG_042828.1:g.8208G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015896.4:c.731G>A MANE Select	NP_056980.2:p.Trp244Ter
ENST00000231749.8:c.731G>A MANE Select	ENSP00000231749.3:p.Trp244Ter
NM_001308379.1:c.716G>A	NP_001295308.1:p.Trp239Ter
NM_001308379.2:c.716G>A	NP_001295308.1:p.Trp239Ter
NM_015896.2:c.731G>A	NP_056980.2:p.Trp244Ter
NM_015896.3:c.731G>A	NP_056980.2:p.Trp244Ter
ENST00000231749.7:c.731G>A	ENSP00000231749.3:p.Trp244Ter
ENST00000360165.7:c.716G>A	ENSP00000353289.3:p.Trp239Ter
ENST00000442887.1:c.602G>A	ENSP00000393687.1:p.Trp201Ter
ENST00000443080.5:c.*483G>A	ENSP00000415661.1:n.*483G>A
ENST00000475688.1:n.630G>A
XM_005265216.2:c.494G>A	XP_005265273.1:p.Trp165Ter
XM_005265216.3:c.494G>A	XP_005265273.1:p.Trp165Ter