Canonical Allele Identifier: CA1363908710

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345362C= , CM000665.2:g.50345362C=	GRCh38
NC_000003.11:g.50382793C= , CM000665.1:g.50382793C=	GRCh37
NC_000003.10:g.50357797C=	NCBI36
NG_023270.1:g.575G=
NG_042828.1:g.5385G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.92+126G= MANE Select	ENSP00000231749.3:n.92+126G=
ENST00000231749.7:c.92+126G=	ENSP00000231749.3:n.92+126G=
ENST00000360165.7:c.92+126G=	ENSP00000353289.3:n.92+126G=
ENST00000431869.1:c.93-126G=	ENSP00000391545.1:n.93-126G=
ENST00000442887.1:c.-37-130G=	ENSP00000393687.1:n.-37-130G=
ENST00000443080.5:c.93-126G=	ENSP00000415661.1:n.93-126G=
ENST00000468182.1:n.194+126G=
NM_001308379.1:c.92+126G=	NP_001295308.1:n.92+126G=
NM_015896.2:c.92+126G=	NP_056980.2:n.92+126G=
NM_015896.3:c.92+126G=	NP_056980.2:n.92+126G=
XM_005265216.2:c.-37+126G=	XP_005265273.1:n.-37+126G=
XM_005265216.3:c.-37+126G=	XP_005265273.1:n.-37+126G=
NM_015896.4:c.92+126G= MANE Select	NP_056980.2:n.92+126G=
NM_001308379.2:c.92+126G=	NP_001295308.1:n.92+126G=