Canonical Allele Identifier: CA1363908802

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345519T= , CM000665.2:g.50345519T=	GRCh38
NC_000003.11:g.50382950T= , CM000665.1:g.50382950T=	GRCh37
NC_000003.10:g.50357954T=	NCBI36
NG_023270.1:g.418A=
NG_042828.1:g.5228A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.61A= MANE Select	ENSP00000231749.3:p.Ser21=
ENST00000231749.7:c.61A=	ENSP00000231749.3:p.Ser21=
ENST00000360165.7:c.61A=	ENSP00000353289.3:p.Ser21=
ENST00000431869.1:c.61A=	ENSP00000391545.1:p.Ser21=
ENST00000442887.1:c.-38+16A=	ENSP00000393687.1:n.-38+16A=
ENST00000443080.5:c.61A=	ENSP00000415661.1:p.Ser21=
ENST00000468182.1:n.163A=
NM_001308379.1:c.61A=	NP_001295308.1:p.Ser21=
NM_015896.2:c.61A=	NP_056980.2:p.Ser21=
NM_015896.3:c.61A=	NP_056980.2:p.Ser21=
XM_005265216.2:c.-68A=	XP_005265273.1:n.-68A=
XM_005265216.3:c.-68A=	XP_005265273.1:n.-68A=
NM_015896.4:c.61A= MANE Select	NP_056980.2:p.Ser21=
NM_001308379.2:c.61A=	NP_001295308.1:p.Ser21=