Canonical Allele Identifier: CA1363903263

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343127C= , CM000665.2:g.50343127C=	GRCh38
NC_000003.11:g.50380558C= , CM000665.1:g.50380558C=	GRCh37
NC_000003.10:g.50355562C=	NCBI36
NG_023270.1:g.2810G=
NG_042828.1:g.7620G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.590G= MANE Select	ENSP00000231749.3:p.Cys197=
ENST00000231749.7:c.590G=	ENSP00000231749.3:p.Cys197=
ENST00000360165.7:c.590G=	ENSP00000353289.3:p.Cys197=
ENST00000442887.1:c.461G=	ENSP00000393687.1:p.Cys154=
ENST00000443080.5:c.*342G=	ENSP00000415661.1:n.*342G=
ENST00000475688.1:n.42G=
NM_001308379.1:c.590G=	NP_001295308.1:p.Cys197=
NM_015896.2:c.590G=	NP_056980.2:p.Cys197=
NM_015896.3:c.590G=	NP_056980.2:p.Cys197=
XM_005265216.2:c.353G=	XP_005265273.1:p.Cys118=
XM_005265216.3:c.353G=	XP_005265273.1:p.Cys118=
NM_015896.4:c.590G= MANE Select	NP_056980.2:p.Cys197=
NM_001308379.2:c.590G=	NP_001295308.1:p.Cys197=