Canonical Allele Identifier: CA1363908667

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345275T= , CM000665.2:g.50345275T=	GRCh38
NC_000003.11:g.50382706T= , CM000665.1:g.50382706T=	GRCh37
NC_000003.10:g.50357710T=	NCBI36
NG_023270.1:g.662A=
NG_042828.1:g.5472A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.93-43A= MANE Select	ENSP00000231749.3:n.93-43A=
ENST00000231749.7:c.93-43A=	ENSP00000231749.3:n.93-43A=
ENST00000360165.7:c.93-43A=	ENSP00000353289.3:n.93-43A=
ENST00000431869.1:c.93-39A=	ENSP00000391545.1:n.93-39A=
ENST00000442887.1:c.-37-43A=	ENSP00000393687.1:n.-37-43A=
ENST00000443080.5:c.93-39A=	ENSP00000415661.1:n.93-39A=
ENST00000468182.1:n.195-43A=
NM_001308379.1:c.93-43A=	NP_001295308.1:n.93-43A=
NM_015896.2:c.93-43A=	NP_056980.2:n.93-43A=
NM_015896.3:c.93-43A=	NP_056980.2:n.93-43A=
XM_005265216.2:c.-37+213A=	XP_005265273.1:n.-37+213A=
XM_005265216.3:c.-37+213A=	XP_005265273.1:n.-37+213A=
NM_015896.4:c.93-43A= MANE Select	NP_056980.2:n.93-43A=
NM_001308379.2:c.93-43A=	NP_001295308.1:n.93-43A=