Canonical Allele Identifier: CA352939751

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342492C>G , CM000665.2:g.50342492C>G	GRCh38
NC_000003.11:g.50379923C>G , CM000665.1:g.50379923C>G	GRCh37
NC_000003.10:g.50354927C>G	NCBI36
NG_023270.1:g.3445G>C
NG_042828.1:g.8255G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_015896.4:c.778G>C MANE Select	NP_056980.2:p.Gly260Arg
ENST00000231749.8:c.778G>C MANE Select	ENSP00000231749.3:p.Gly260Arg
NM_001308379.1:c.763G>C	NP_001295308.1:p.Gly255Arg
NM_001308379.2:c.763G>C	NP_001295308.1:p.Gly255Arg
NM_015896.2:c.778G>C	NP_056980.2:p.Gly260Arg
NM_015896.3:c.778G>C	NP_056980.2:p.Gly260Arg
ENST00000231749.7:c.778G>C	ENSP00000231749.3:p.Gly260Arg
ENST00000360165.7:c.763G>C	ENSP00000353289.3:p.Gly255Arg
ENST00000442887.1:c.649G>C	ENSP00000393687.1:p.Gly217Arg
ENST00000475688.1:n.677G>C
XM_005265216.2:c.541G>C	XP_005265273.1:p.Gly181Arg
XM_005265216.3:c.541G>C	XP_005265273.1:p.Gly181Arg