Canonical Allele Identifier: CA1363903115

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342983G= , CM000665.2:g.50342983G=	GRCh38
NC_000003.11:g.50380414G= , CM000665.1:g.50380414G=	GRCh37
NC_000003.10:g.50355418G=	NCBI36
NG_023270.1:g.2954C=
NG_042828.1:g.7764C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.635C= MANE Select	ENSP00000231749.3:p.Thr212=
ENST00000231749.7:c.635C=	ENSP00000231749.3:p.Thr212=
ENST00000360165.7:c.599+135C=	ENSP00000353289.3:n.599+135C=
ENST00000442887.1:c.506C=	ENSP00000393687.1:p.Thr169=
ENST00000443080.5:c.*387C=	ENSP00000415661.1:n.*387C=
ENST00000475688.1:n.186C=
NM_001308379.1:c.599+135C=	NP_001295308.1:n.599+135C=
NM_015896.2:c.635C=	NP_056980.2:p.Thr212=
NM_015896.3:c.635C=	NP_056980.2:p.Thr212=
XM_005265216.2:c.398C=	XP_005265273.1:p.Thr133=
XM_005265216.3:c.398C=	XP_005265273.1:p.Thr133=
NM_015896.4:c.635C= MANE Select	NP_056980.2:p.Thr212=
NM_001308379.2:c.599+135C=	NP_001295308.1:n.599+135C=