Canonical Allele Identifier: CA2756211692

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343027A>T , CM000665.2:g.50343027A>T	GRCh38
NC_000003.11:g.50380458A>T , CM000665.1:g.50380458A>T	GRCh37
NC_000003.10:g.50355462A>T	NCBI36
NG_023270.1:g.2910T>A
NG_042828.1:g.7720T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.600-9T>A MANE Select	ENSP00000231749.3:n.600-9T>A
ENST00000231749.7:c.600-9T>A	ENSP00000231749.3:n.600-9T>A
ENST00000360165.7:c.599+91T>A	ENSP00000353289.3:n.599+91T>A
ENST00000442887.1:c.471-9T>A	ENSP00000393687.1:n.471-9T>A
ENST00000443080.5:c.*352-9T>A	ENSP00000415661.1:n.*352-9T>A
ENST00000475688.1:n.142T>A
NM_001308379.1:c.599+91T>A	NP_001295308.1:n.599+91T>A
NM_015896.2:c.600-9T>A	NP_056980.2:n.600-9T>A
NM_015896.3:c.600-9T>A	NP_056980.2:n.600-9T>A
XM_005265216.2:c.363-9T>A	XP_005265273.1:n.363-9T>A
XM_005265216.3:c.363-9T>A	XP_005265273.1:n.363-9T>A
NM_015896.4:c.600-9T>A MANE Select	NP_056980.2:n.600-9T>A
NM_001308379.2:c.599+91T>A	NP_001295308.1:n.599+91T>A