Canonical Allele Identifier: CA352941999

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380447A>T (hg19) ; chr3:g.50343016A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343016A>T , CM000665.2:g.50343016A>T	GRCh38
NC_000003.11:g.50380447A>T , CM000665.1:g.50380447A>T	GRCh37
NC_000003.10:g.50355451A>T	NCBI36
NG_023270.1:g.2921T>A
NG_042828.1:g.7731T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.602T>A MANE Select	ENSP00000231749.3:p.Leu201His
ENST00000231749.7:c.602T>A	ENSP00000231749.3:p.Leu201His
ENST00000360165.7:c.599+102T>A	ENSP00000353289.3:n.599+102T>A
ENST00000442887.1:c.473T>A	ENSP00000393687.1:p.Leu158His
ENST00000443080.5:c.*354T>A	ENSP00000415661.1:n.*354T>A
ENST00000475688.1:n.153T>A
NM_001308379.1:c.599+102T>A	NP_001295308.1:n.599+102T>A
NM_015896.2:c.602T>A	NP_056980.2:p.Leu201His
NM_015896.3:c.602T>A	NP_056980.2:p.Leu201His
XM_005265216.2:c.365T>A	XP_005265273.1:p.Leu122His
XM_005265216.3:c.365T>A	XP_005265273.1:p.Leu122His
NM_015896.4:c.602T>A MANE Select	NP_056980.2:p.Leu201His
NM_001308379.2:c.599+102T>A	NP_001295308.1:n.599+102T>A