Canonical Allele Identifier: CA1363903271

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343136A= , CM000665.2:g.50343136A=	GRCh38
NC_000003.11:g.50380567A= , CM000665.1:g.50380567A=	GRCh37
NC_000003.10:g.50355571A=	NCBI36
NG_023270.1:g.2801T=
NG_042828.1:g.7611T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.581T= MANE Select	ENSP00000231749.3:p.Ile194=
ENST00000231749.7:c.581T=	ENSP00000231749.3:p.Ile194=
ENST00000360165.7:c.581T=	ENSP00000353289.3:p.Ile194=
ENST00000442887.1:c.452T=	ENSP00000393687.1:p.Ile151=
ENST00000443080.5:c.*333T=	ENSP00000415661.1:n.*333T=
ENST00000475688.1:n.33T=
NM_001308379.1:c.581T=	NP_001295308.1:p.Ile194=
NM_015896.2:c.581T=	NP_056980.2:p.Ile194=
NM_015896.3:c.581T=	NP_056980.2:p.Ile194=
XM_005265216.2:c.344T=	XP_005265273.1:p.Ile115=
XM_005265216.3:c.344T=	XP_005265273.1:p.Ile115=
NM_015896.4:c.581T= MANE Select	NP_056980.2:p.Ile194=
NM_001308379.2:c.581T=	NP_001295308.1:p.Ile194=