Canonical Allele Identifier: CA1363902086

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342047G= , CM000665.2:g.50342047G=	GRCh38
NC_000003.11:g.50379478G= , CM000665.1:g.50379478G=	GRCh37
NC_000003.10:g.50354482G=	NCBI36
NG_023270.1:g.3890C=
NG_042828.1:g.8700C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.967C= MANE Select	ENSP00000231749.3:p.Gln323=
ENST00000231749.7:c.967C=	ENSP00000231749.3:p.Gln323=
ENST00000360165.7:c.952C=	ENSP00000353289.3:p.Gln318=
ENST00000442887.1:c.838C=	ENSP00000393687.1:p.Gln280=
ENST00000475688.1:n.1122C=
ENST00000490675.5:n.53-116C=
NM_001308379.1:c.952C=	NP_001295308.1:p.Gln318=
NM_015896.2:c.967C=	NP_056980.2:p.Gln323=
NM_015896.3:c.967C=	NP_056980.2:p.Gln323=
XM_005265216.2:c.730C=	XP_005265273.1:p.Gln244=
XM_005265216.3:c.730C=	XP_005265273.1:p.Gln244=
NM_015896.4:c.967C= MANE Select	NP_056980.2:p.Gln323=
NM_001308379.2:c.952C=	NP_001295308.1:p.Gln318=