Canonical Allele Identifier: CA433711566

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50383060C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345629C>A , CM000665.2:g.50345629C>A	GRCh38
NC_000003.11:g.50383060C>A , CM000665.1:g.50383060C>A	GRCh37
NC_000003.10:g.50358064C>A	NCBI36
NG_023270.1:g.308G>T
NG_042828.1:g.5118G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-50G>T MANE Select	ENSP00000231749.3:n.-50G>T
ENST00000231749.7:c.-50G>T	ENSP00000231749.3:n.-50G>T
ENST00000360165.7:c.-50G>T	ENSP00000353289.3:n.-50G>T
ENST00000431869.1:c.-50G>T	ENSP00000391545.1:n.-50G>T
ENST00000442887.1:c.-132G>T	ENSP00000393687.1:n.-132G>T
ENST00000443080.5:c.-50G>T	ENSP00000415661.1:n.-50G>T
ENST00000468182.1:n.53G>T
NM_001308379.1:c.-50G>T	NP_001295308.1:n.-50G>T
NM_015896.2:c.-50G>T	NP_056980.2:n.-50G>T
NM_015896.3:c.-50G>T	NP_056980.2:n.-50G>T
XM_005265216.2:c.-178G>T	XP_005265273.1:n.-178G>T
XM_005265216.3:c.-178G>T	XP_005265273.1:n.-178G>T
NM_015896.4:c.-50G>T MANE Select	NP_056980.2:n.-50G>T
NM_001308379.2:c.-50G>T	NP_001295308.1:n.-50G>T