Canonical Allele Identifier: CA433709008

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380368G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342937G>T , CM000665.2:g.50342937G>T	GRCh38
NC_000003.11:g.50380368G>T , CM000665.1:g.50380368G>T	GRCh37
NC_000003.10:g.50355372G>T	NCBI36
NG_023270.1:g.3000C>A
NG_042828.1:g.7810C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.681C>A MANE Select	ENSP00000231749.3:p.Pro227=
ENST00000231749.7:c.681C>A	ENSP00000231749.3:p.Pro227=
ENST00000360165.7:c.599+181C>A	ENSP00000353289.3:n.599+181C>A
ENST00000442887.1:c.552C>A	ENSP00000393687.1:p.Pro184=
ENST00000443080.5:c.*433C>A	ENSP00000415661.1:n.*433C>A
ENST00000475688.1:n.232C>A
NM_001308379.1:c.599+181C>A	NP_001295308.1:n.599+181C>A
NM_015896.2:c.681C>A	NP_056980.2:p.Pro227=
NM_015896.3:c.681C>A	NP_056980.2:p.Pro227=
XM_005265216.2:c.444C>A	XP_005265273.1:p.Pro148=
XM_005265216.3:c.444C>A	XP_005265273.1:p.Pro148=
NM_015896.4:c.681C>A MANE Select	NP_056980.2:p.Pro227=
NM_001308379.2:c.599+181C>A	NP_001295308.1:n.599+181C>A