Canonical Allele Identifier: CA352942281

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380621G>T (hg19) ; chr3:g.50343190G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343190G>T , CM000665.2:g.50343190G>T	GRCh38
NC_000003.11:g.50380621G>T , CM000665.1:g.50380621G>T	GRCh37
NC_000003.10:g.50355625G>T	NCBI36
NG_023270.1:g.2747C>A
NG_042828.1:g.7557C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.527C>A MANE Select	ENSP00000231749.3:p.Ala176Glu
ENST00000231749.7:c.527C>A	ENSP00000231749.3:p.Ala176Glu
ENST00000360165.7:c.527C>A	ENSP00000353289.3:p.Ala176Glu
ENST00000442887.1:c.398C>A	ENSP00000393687.1:p.Ala133Glu
ENST00000443080.5:c.*279C>A	ENSP00000415661.1:n.*279C>A
ENST00000478269.5:n.612C>A
NM_001308379.1:c.527C>A	NP_001295308.1:p.Ala176Glu
NM_015896.2:c.527C>A	NP_056980.2:p.Ala176Glu
NM_015896.3:c.527C>A	NP_056980.2:p.Ala176Glu
XM_005265216.2:c.290C>A	XP_005265273.1:p.Ala97Glu
XM_005265216.3:c.290C>A	XP_005265273.1:p.Ala97Glu
NM_015896.4:c.527C>A MANE Select	NP_056980.2:p.Ala176Glu
NM_001308379.2:c.527C>A	NP_001295308.1:p.Ala176Glu