Canonical Allele Identifier: CA1363908830

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345578A= , CM000665.2:g.50345578A=	GRCh38
NC_000003.11:g.50383009A= , CM000665.1:g.50383009A=	GRCh37
NC_000003.10:g.50358013A=	NCBI36
NG_023270.1:g.359T=
NG_042828.1:g.5169T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.2T= MANE Select	ENSP00000231749.3:p.Met1=
ENST00000231749.7:c.2T=	ENSP00000231749.3:p.Met1=
ENST00000360165.7:c.2T=	ENSP00000353289.3:p.Met1=
ENST00000431869.1:c.2T=	ENSP00000391545.1:p.Met1=
ENST00000442887.1:c.-81T=	ENSP00000393687.1:n.-81T=
ENST00000443080.5:c.2T=	ENSP00000415661.1:p.Met1=
ENST00000468182.1:n.104T=
NM_001308379.1:c.2T=	NP_001295308.1:p.Met1=
NM_015896.2:c.2T=	NP_056980.2:p.Met1=
NM_015896.3:c.2T=	NP_056980.2:p.Met1=
XM_005265216.2:c.-127T=	XP_005265273.1:n.-127T=
XM_005265216.3:c.-127T=	XP_005265273.1:n.-127T=
NM_015896.4:c.2T= MANE Select	NP_056980.2:p.Met1=
NM_001308379.2:c.2T=	NP_001295308.1:p.Met1=