Canonical Allele Identifier: CA1363902549

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342473A= , CM000665.2:g.50342473A=	GRCh38
NC_000003.11:g.50379904A= , CM000665.1:g.50379904A=	GRCh37
NC_000003.10:g.50354908A=	NCBI36
NG_023270.1:g.3464T=
NG_042828.1:g.8274T=

Transcript Alleles

HGVS	Amino-acid Change
NM_015896.4:c.797T= MANE Select	NP_056980.2:p.Leu266=
ENST00000231749.8:c.797T= MANE Select	ENSP00000231749.3:p.Leu266=
NM_001308379.1:c.782T=	NP_001295308.1:p.Leu261=
NM_001308379.2:c.782T=	NP_001295308.1:p.Leu261=
NM_015896.2:c.797T=	NP_056980.2:p.Leu266=
NM_015896.3:c.797T=	NP_056980.2:p.Leu266=
ENST00000231749.7:c.797T=	ENSP00000231749.3:p.Leu266=
ENST00000360165.7:c.782T=	ENSP00000353289.3:p.Leu261=
ENST00000442887.1:c.668T=	ENSP00000393687.1:p.Leu223=
ENST00000475688.1:n.696T=
XM_005265216.2:c.560T=	XP_005265273.1:p.Leu187=
XM_005265216.3:c.560T=	XP_005265273.1:p.Leu187=