Canonical Allele Identifier: CA352941669

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380372C>T (hg19) ; chr3:g.50342941C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342941C>T , CM000665.2:g.50342941C>T	GRCh38
NC_000003.11:g.50380372C>T , CM000665.1:g.50380372C>T	GRCh37
NC_000003.10:g.50355376C>T	NCBI36
NG_023270.1:g.2996G>A
NG_042828.1:g.7806G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.677G>A MANE Select	ENSP00000231749.3:p.Ser226Asn
ENST00000231749.7:c.677G>A	ENSP00000231749.3:p.Ser226Asn
ENST00000360165.7:c.599+177G>A	ENSP00000353289.3:n.599+177G>A
ENST00000442887.1:c.548G>A	ENSP00000393687.1:p.Ser183Asn
ENST00000443080.5:c.*429G>A	ENSP00000415661.1:n.*429G>A
ENST00000475688.1:n.228G>A
NM_001308379.1:c.599+177G>A	NP_001295308.1:n.599+177G>A
NM_015896.2:c.677G>A	NP_056980.2:p.Ser226Asn
NM_015896.3:c.677G>A	NP_056980.2:p.Ser226Asn
XM_005265216.2:c.440G>A	XP_005265273.1:p.Ser147Asn
XM_005265216.3:c.440G>A	XP_005265273.1:p.Ser147Asn
NM_015896.4:c.677G>A MANE Select	NP_056980.2:p.Ser226Asn
NM_001308379.2:c.599+177G>A	NP_001295308.1:n.599+177G>A