Canonical Allele Identifier: CA352942069

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380560G>T (hg19) ; chr3:g.50343129G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343129G>T , CM000665.2:g.50343129G>T	GRCh38
NC_000003.11:g.50380560G>T , CM000665.1:g.50380560G>T	GRCh37
NC_000003.10:g.50355564G>T	NCBI36
NG_023270.1:g.2808C>A
NG_042828.1:g.7618C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.588C>A MANE Select	ENSP00000231749.3:p.Asp196Glu
ENST00000231749.7:c.588C>A	ENSP00000231749.3:p.Asp196Glu
ENST00000360165.7:c.588C>A	ENSP00000353289.3:p.Asp196Glu
ENST00000442887.1:c.459C>A	ENSP00000393687.1:p.Asp153Glu
ENST00000443080.5:c.*340C>A	ENSP00000415661.1:n.*340C>A
ENST00000475688.1:n.40C>A
NM_001308379.1:c.588C>A	NP_001295308.1:p.Asp196Glu
NM_015896.2:c.588C>A	NP_056980.2:p.Asp196Glu
NM_015896.3:c.588C>A	NP_056980.2:p.Asp196Glu
XM_005265216.2:c.351C>A	XP_005265273.1:p.Asp117Glu
XM_005265216.3:c.351C>A	XP_005265273.1:p.Asp117Glu
NM_015896.4:c.588C>A MANE Select	NP_056980.2:p.Asp196Glu
NM_001308379.2:c.588C>A	NP_001295308.1:p.Asp196Glu