Canonical Allele Identifier: CA433710321

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382603T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345172T>A , CM000665.2:g.50345172T>A	GRCh38
NC_000003.11:g.50382603T>A , CM000665.1:g.50382603T>A	GRCh37
NC_000003.10:g.50357607T>A	NCBI36
NG_023270.1:g.765A>T
NG_042828.1:g.5575A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.153A>T MANE Select	ENSP00000231749.3:p.Thr51=
ENST00000231749.7:c.153A>T	ENSP00000231749.3:p.Thr51=
ENST00000360165.7:c.153A>T	ENSP00000353289.3:p.Thr51=
ENST00000431869.1:c.*43A>T	ENSP00000391545.1:n.*43A>T
ENST00000442887.1:c.24A>T	ENSP00000393687.1:p.Thr8=
ENST00000443080.5:c.*43A>T	ENSP00000415661.1:n.*43A>T
ENST00000468182.1:n.255A>T
NM_001308379.1:c.153A>T	NP_001295308.1:p.Thr51=
NM_015896.2:c.153A>T	NP_056980.2:p.Thr51=
NM_015896.3:c.153A>T	NP_056980.2:p.Thr51=
XM_005265216.2:c.-37+316A>T	XP_005265273.1:n.-37+316A>T
XM_005265216.3:c.-37+316A>T	XP_005265273.1:n.-37+316A>T
NM_015896.4:c.153A>T MANE Select	NP_056980.2:p.Thr51=
NM_001308379.2:c.153A>T	NP_001295308.1:p.Thr51=