Canonical Allele Identifier: CA352942193

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380597G>T (hg19) ; chr3:g.50343166G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343166G>T , CM000665.2:g.50343166G>T	GRCh38
NC_000003.11:g.50380597G>T , CM000665.1:g.50380597G>T	GRCh37
NC_000003.10:g.50355601G>T	NCBI36
NG_023270.1:g.2771C>A
NG_042828.1:g.7581C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.551C>A MANE Select	ENSP00000231749.3:p.Ala184Glu
ENST00000231749.7:c.551C>A	ENSP00000231749.3:p.Ala184Glu
ENST00000360165.7:c.551C>A	ENSP00000353289.3:p.Ala184Glu
ENST00000442887.1:c.422C>A	ENSP00000393687.1:p.Ala141Glu
ENST00000443080.5:c.*303C>A	ENSP00000415661.1:n.*303C>A
ENST00000475688.1:n.3C>A
NM_001308379.1:c.551C>A	NP_001295308.1:p.Ala184Glu
NM_015896.2:c.551C>A	NP_056980.2:p.Ala184Glu
NM_015896.3:c.551C>A	NP_056980.2:p.Ala184Glu
XM_005265216.2:c.314C>A	XP_005265273.1:p.Ala105Glu
XM_005265216.3:c.314C>A	XP_005265273.1:p.Ala105Glu
NM_015896.4:c.551C>A MANE Select	NP_056980.2:p.Ala184Glu
NM_001308379.2:c.551C>A	NP_001295308.1:p.Ala184Glu