Canonical Allele Identifier: CA1363903375

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343281C= , CM000665.2:g.50343281C=	GRCh38
NC_000003.11:g.50380712C= , CM000665.1:g.50380712C=	GRCh37
NC_000003.10:g.50355716C=	NCBI36
NG_023270.1:g.2656G=
NG_042828.1:g.7466G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.510+26G= MANE Select	ENSP00000231749.3:n.510+26G=
ENST00000231749.7:c.510+26G=	ENSP00000231749.3:n.510+26G=
ENST00000360165.7:c.510+26G=	ENSP00000353289.3:n.510+26G=
ENST00000442887.1:c.381+26G=	ENSP00000393687.1:n.381+26G=
ENST00000443080.5:c.*263-75G=	ENSP00000415661.1:n.*263-75G=
ENST00000478269.5:n.521G=
NM_001308379.1:c.510+26G=	NP_001295308.1:n.510+26G=
NM_015896.2:c.510+26G=	NP_056980.2:n.510+26G=
NM_015896.3:c.510+26G=	NP_056980.2:n.510+26G=
XM_005265216.2:c.273+26G=	XP_005265273.1:n.273+26G=
XM_005265216.3:c.273+26G=	XP_005265273.1:n.273+26G=
NM_015896.4:c.510+26G= MANE Select	NP_056980.2:n.510+26G=
NM_001308379.2:c.510+26G=	NP_001295308.1:n.510+26G=