Canonical Allele Identifier: CA1363903269

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343133G= , CM000665.2:g.50343133G=	GRCh38
NC_000003.11:g.50380564G= , CM000665.1:g.50380564G=	GRCh37
NC_000003.10:g.50355568G=	NCBI36
NG_023270.1:g.2804C=
NG_042828.1:g.7614C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.584C= MANE Select	ENSP00000231749.3:p.Thr195=
ENST00000231749.7:c.584C=	ENSP00000231749.3:p.Thr195=
ENST00000360165.7:c.584C=	ENSP00000353289.3:p.Thr195=
ENST00000442887.1:c.455C=	ENSP00000393687.1:p.Thr152=
ENST00000443080.5:c.*336C=	ENSP00000415661.1:n.*336C=
ENST00000475688.1:n.36C=
NM_001308379.1:c.584C=	NP_001295308.1:p.Thr195=
NM_015896.2:c.584C=	NP_056980.2:p.Thr195=
NM_015896.3:c.584C=	NP_056980.2:p.Thr195=
XM_005265216.2:c.347C=	XP_005265273.1:p.Thr116=
XM_005265216.3:c.347C=	XP_005265273.1:p.Thr116=
NM_015896.4:c.584C= MANE Select	NP_056980.2:p.Thr195=
NM_001308379.2:c.584C=	NP_001295308.1:p.Thr195=