Canonical Allele Identifier: CA352942279

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380619C>T (hg19) ; chr3:g.50343188C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343188C>T , CM000665.2:g.50343188C>T	GRCh38
NC_000003.11:g.50380619C>T , CM000665.1:g.50380619C>T	GRCh37
NC_000003.10:g.50355623C>T	NCBI36
NG_023270.1:g.2749G>A
NG_042828.1:g.7559G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.529G>A MANE Select	ENSP00000231749.3:p.Glu177Lys
ENST00000231749.7:c.529G>A	ENSP00000231749.3:p.Glu177Lys
ENST00000360165.7:c.529G>A	ENSP00000353289.3:p.Glu177Lys
ENST00000442887.1:c.400G>A	ENSP00000393687.1:p.Glu134Lys
ENST00000443080.5:c.*281G>A	ENSP00000415661.1:n.*281G>A
ENST00000478269.5:n.614G>A
NM_001308379.1:c.529G>A	NP_001295308.1:p.Glu177Lys
NM_015896.2:c.529G>A	NP_056980.2:p.Glu177Lys
NM_015896.3:c.529G>A	NP_056980.2:p.Glu177Lys
XM_005265216.2:c.292G>A	XP_005265273.1:p.Glu98Lys
XM_005265216.3:c.292G>A	XP_005265273.1:p.Glu98Lys
NM_015896.4:c.529G>A MANE Select	NP_056980.2:p.Glu177Lys
NM_001308379.2:c.529G>A	NP_001295308.1:p.Glu177Lys