Canonical Allele Identifier: CA1363903246

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1703439928

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343114T>A , CM000665.2:g.50343114T>A	GRCh38
NC_000003.11:g.50380545T>A , CM000665.1:g.50380545T>A	GRCh37
NC_000003.10:g.50355549T>A	NCBI36
NG_023270.1:g.2823A>T
NG_042828.1:g.7633A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.599+4A>T MANE Select	ENSP00000231749.3:n.599+4A>T
ENST00000231749.7:c.599+4A>T	ENSP00000231749.3:n.599+4A>T
ENST00000360165.7:c.599+4A>T	ENSP00000353289.3:n.599+4A>T
ENST00000442887.1:c.470+4A>T	ENSP00000393687.1:n.470+4A>T
ENST00000443080.5:c.*351+4A>T	ENSP00000415661.1:n.*351+4A>T
ENST00000475688.1:n.55A>T
NM_001308379.1:c.599+4A>T	NP_001295308.1:n.599+4A>T
NM_015896.2:c.599+4A>T	NP_056980.2:n.599+4A>T
NM_015896.3:c.599+4A>T	NP_056980.2:n.599+4A>T
XM_005265216.2:c.362+4A>T	XP_005265273.1:n.362+4A>T
XM_005265216.3:c.362+4A>T	XP_005265273.1:n.362+4A>T
NM_015896.4:c.599+4A>T MANE Select	NP_056980.2:n.599+4A>T
NM_001308379.2:c.599+4A>T	NP_001295308.1:n.599+4A>T