Canonical Allele Identifier: CA352945917

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50345490-T-A
• MyVariant Identifiers: chr3:g.50382921T>A (hg19) ; chr3:g.50345490T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345490T>A , CM000665.2:g.50345490T>A	GRCh38
NC_000003.11:g.50382921T>A , CM000665.1:g.50382921T>A	GRCh37
NC_000003.10:g.50357925T>A	NCBI36
NG_023270.1:g.447A>T
NG_042828.1:g.5257A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.90A>T MANE Select	ENSP00000231749.3:p.Glu30Asp
ENST00000231749.7:c.90A>T	ENSP00000231749.3:p.Glu30Asp
ENST00000360165.7:c.90A>T	ENSP00000353289.3:p.Glu30Asp
ENST00000431869.1:c.90A>T	ENSP00000391545.1:p.Glu30Asp
ENST00000442887.1:c.-38+45A>T	ENSP00000393687.1:n.-38+45A>T
ENST00000443080.5:c.90A>T	ENSP00000415661.1:p.Glu30Asp
ENST00000468182.1:n.192A>T
NM_001308379.1:c.90A>T	NP_001295308.1:p.Glu30Asp
NM_015896.2:c.90A>T	NP_056980.2:p.Glu30Asp
NM_015896.3:c.90A>T	NP_056980.2:p.Glu30Asp
XM_005265216.2:c.-39A>T	XP_005265273.1:n.-39A>T
XM_005265216.3:c.-39A>T	XP_005265273.1:n.-39A>T
NM_015896.4:c.90A>T MANE Select	NP_056980.2:p.Glu30Asp
NM_001308379.2:c.90A>T	NP_001295308.1:p.Glu30Asp