Canonical Allele Identifier: CA1363908629

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345181G= , CM000665.2:g.50345181G=	GRCh38
NC_000003.11:g.50382612G= , CM000665.1:g.50382612G=	GRCh37
NC_000003.10:g.50357616G=	NCBI36
NG_023270.1:g.756C=
NG_042828.1:g.5566C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.144C= MANE Select	ENSP00000231749.3:p.Leu48=
ENST00000231749.7:c.144C=	ENSP00000231749.3:p.Leu48=
ENST00000360165.7:c.144C=	ENSP00000353289.3:p.Leu48=
ENST00000431869.1:c.*34C=	ENSP00000391545.1:n.*34C=
ENST00000442887.1:c.15C=	ENSP00000393687.1:p.Leu5=
ENST00000443080.5:c.*34C=	ENSP00000415661.1:n.*34C=
ENST00000468182.1:n.246C=
NM_001308379.1:c.144C=	NP_001295308.1:p.Leu48=
NM_015896.2:c.144C=	NP_056980.2:p.Leu48=
NM_015896.3:c.144C=	NP_056980.2:p.Leu48=
XM_005265216.2:c.-37+307C=	XP_005265273.1:n.-37+307C=
XM_005265216.3:c.-37+307C=	XP_005265273.1:n.-37+307C=
NM_015896.4:c.144C= MANE Select	NP_056980.2:p.Leu48=
NM_001308379.2:c.144C=	NP_001295308.1:p.Leu48=