Canonical Allele Identifier: CA352945579

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382601A>T (hg19) ; chr3:g.50345170A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345170A>T , CM000665.2:g.50345170A>T	GRCh38
NC_000003.11:g.50382601A>T , CM000665.1:g.50382601A>T	GRCh37
NC_000003.10:g.50357605A>T	NCBI36
NG_023270.1:g.767T>A
NG_042828.1:g.5577T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.155T>A MANE Select	ENSP00000231749.3:p.Val52Asp
ENST00000231749.7:c.155T>A	ENSP00000231749.3:p.Val52Asp
ENST00000360165.7:c.155T>A	ENSP00000353289.3:p.Val52Asp
ENST00000431869.1:c.*45T>A	ENSP00000391545.1:n.*45T>A
ENST00000442887.1:c.26T>A	ENSP00000393687.1:p.Val9Asp
ENST00000443080.5:c.*45T>A	ENSP00000415661.1:n.*45T>A
ENST00000468182.1:n.257T>A
NM_001308379.1:c.155T>A	NP_001295308.1:p.Val52Asp
NM_015896.2:c.155T>A	NP_056980.2:p.Val52Asp
NM_015896.3:c.155T>A	NP_056980.2:p.Val52Asp
XM_005265216.2:c.-37+318T>A	XP_005265273.1:n.-37+318T>A
XM_005265216.3:c.-37+318T>A	XP_005265273.1:n.-37+318T>A
NM_015896.4:c.155T>A MANE Select	NP_056980.2:p.Val52Asp
NM_001308379.2:c.155T>A	NP_001295308.1:p.Val52Asp