Canonical Allele Identifier: CA2416992

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50341813C>T , CM000665.2:g.50341813C>T	GRCh38
NC_000003.11:g.50379244C>T , CM000665.1:g.50379244C>T	GRCh37
NC_000003.10:g.50354248C>T	NCBI36
NG_023270.1:g.4124G>A
NG_042828.1:g.8934G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015896.4:c.1118G>A MANE Select	NP_056980.2:p.Arg373Gln
ENST00000231749.8:c.1118G>A MANE Select	ENSP00000231749.3:p.Arg373Gln
NM_001308379.1:c.1103G>A	NP_001295308.1:p.Arg368Gln
NM_001308379.2:c.1103G>A	NP_001295308.1:p.Arg368Gln
NM_015896.2:c.1118G>A	NP_056980.2:p.Arg373Gln
NM_015896.3:c.1118G>A	NP_056980.2:p.Arg373Gln
ENST00000231749.7:c.1118G>A	ENSP00000231749.3:p.Arg373Gln
ENST00000360165.7:c.1103G>A	ENSP00000353289.3:p.Arg368Gln
ENST00000475688.1:n.1273G>A
ENST00000490675.5:n.171G>A
XM_005265216.2:c.881G>A	XP_005265273.1:p.Arg294Gln
XM_005265216.3:c.881G>A	XP_005265273.1:p.Arg294Gln