Canonical Allele Identifier: CA433710251

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382582A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345151A>G , CM000665.2:g.50345151A>G	GRCh38
NC_000003.11:g.50382582A>G , CM000665.1:g.50382582A>G	GRCh37
NC_000003.10:g.50357586A>G	NCBI36
NG_023270.1:g.786T>C
NG_042828.1:g.5596T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.174T>C MANE Select	ENSP00000231749.3:p.Ile58=
ENST00000231749.7:c.174T>C	ENSP00000231749.3:p.Ile58=
ENST00000360165.7:c.174T>C	ENSP00000353289.3:p.Ile58=
ENST00000431869.1:c.*64T>C	ENSP00000391545.1:n.*64T>C
ENST00000442887.1:c.45T>C	ENSP00000393687.1:p.Ile15=
ENST00000443080.5:c.*64T>C	ENSP00000415661.1:n.*64T>C
ENST00000468182.1:n.276T>C
NM_001308379.1:c.174T>C	NP_001295308.1:p.Ile58=
NM_015896.2:c.174T>C	NP_056980.2:p.Ile58=
NM_015896.3:c.174T>C	NP_056980.2:p.Ile58=
XM_005265216.2:c.-37+337T>C	XP_005265273.1:n.-37+337T>C
XM_005265216.3:c.-37+337T>C	XP_005265273.1:n.-37+337T>C
NM_015896.4:c.174T>C MANE Select	NP_056980.2:p.Ile58=
NM_001308379.2:c.174T>C	NP_001295308.1:p.Ile58=