Canonical Allele Identifier: CA1363903255

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343122C= , CM000665.2:g.50343122C=	GRCh38
NC_000003.11:g.50380553C= , CM000665.1:g.50380553C=	GRCh37
NC_000003.10:g.50355557C=	NCBI36
NG_023270.1:g.2815G=
NG_042828.1:g.7625G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.595G= MANE Select	ENSP00000231749.3:p.Asp199=
ENST00000231749.7:c.595G=	ENSP00000231749.3:p.Asp199=
ENST00000360165.7:c.595G=	ENSP00000353289.3:p.Asp199=
ENST00000442887.1:c.466G=	ENSP00000393687.1:p.Asp156=
ENST00000443080.5:c.*347G=	ENSP00000415661.1:n.*347G=
ENST00000475688.1:n.47G=
NM_001308379.1:c.595G=	NP_001295308.1:p.Asp199=
NM_015896.2:c.595G=	NP_056980.2:p.Asp199=
NM_015896.3:c.595G=	NP_056980.2:p.Asp199=
XM_005265216.2:c.358G=	XP_005265273.1:p.Asp120=
XM_005265216.3:c.358G=	XP_005265273.1:p.Asp120=
NM_015896.4:c.595G= MANE Select	NP_056980.2:p.Asp199=
NM_001308379.2:c.595G=	NP_001295308.1:p.Asp199=