Canonical Allele Identifier: CA1363903308

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343190G= , CM000665.2:g.50343190G=	GRCh38
NC_000003.11:g.50380621G= , CM000665.1:g.50380621G=	GRCh37
NC_000003.10:g.50355625G=	NCBI36
NG_023270.1:g.2747C=
NG_042828.1:g.7557C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.527C= MANE Select	ENSP00000231749.3:p.Ala176=
ENST00000231749.7:c.527C=	ENSP00000231749.3:p.Ala176=
ENST00000360165.7:c.527C=	ENSP00000353289.3:p.Ala176=
ENST00000442887.1:c.398C=	ENSP00000393687.1:p.Ala133=
ENST00000443080.5:c.*279C=	ENSP00000415661.1:n.*279C=
ENST00000478269.5:n.612C=
NM_001308379.1:c.527C=	NP_001295308.1:p.Ala176=
NM_015896.2:c.527C=	NP_056980.2:p.Ala176=
NM_015896.3:c.527C=	NP_056980.2:p.Ala176=
XM_005265216.2:c.290C=	XP_005265273.1:p.Ala97=
XM_005265216.3:c.290C=	XP_005265273.1:p.Ala97=
NM_015896.4:c.527C= MANE Select	NP_056980.2:p.Ala176=
NM_001308379.2:c.527C=	NP_001295308.1:p.Ala176=