Canonical Allele Identifier: CA1363903350

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343257T= , CM000665.2:g.50343257T=	GRCh38
NC_000003.11:g.50380688T= , CM000665.1:g.50380688T=	GRCh37
NC_000003.10:g.50355692T=	NCBI36
NG_023270.1:g.2680A=
NG_042828.1:g.7490A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.511-51A= MANE Select	ENSP00000231749.3:n.511-51A=
ENST00000231749.7:c.511-51A=	ENSP00000231749.3:n.511-51A=
ENST00000360165.7:c.511-51A=	ENSP00000353289.3:n.511-51A=
ENST00000442887.1:c.382-51A=	ENSP00000393687.1:n.382-51A=
ENST00000443080.5:c.*263-51A=	ENSP00000415661.1:n.*263-51A=
ENST00000478269.5:n.545A=
NM_001308379.1:c.511-51A=	NP_001295308.1:n.511-51A=
NM_015896.2:c.511-51A=	NP_056980.2:n.511-51A=
NM_015896.3:c.511-51A=	NP_056980.2:n.511-51A=
XM_005265216.2:c.274-51A=	XP_005265273.1:n.274-51A=
XM_005265216.3:c.274-51A=	XP_005265273.1:n.274-51A=
NM_015896.4:c.511-51A= MANE Select	NP_056980.2:n.511-51A=
NM_001308379.2:c.511-51A=	NP_001295308.1:n.511-51A=