Canonical Allele Identifier: CA2417196

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343327G>A , CM000665.2:g.50343327G>A	GRCh38
NC_000003.11:g.50380758G>A , CM000665.1:g.50380758G>A	GRCh37
NC_000003.10:g.50355762G>A	NCBI36
NG_023270.1:g.2610C>T
NG_042828.1:g.7420C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015896.4:c.490C>T MANE Select	NP_056980.2:p.Gln164Ter
ENST00000231749.8:c.490C>T MANE Select	ENSP00000231749.3:p.Gln164Ter
NM_001308379.1:c.490C>T	NP_001295308.1:p.Gln164Ter
NM_001308379.2:c.490C>T	NP_001295308.1:p.Gln164Ter
NM_015896.2:c.490C>T	NP_056980.2:p.Gln164Ter
NM_015896.3:c.490C>T	NP_056980.2:p.Gln164Ter
ENST00000231749.7:c.490C>T	ENSP00000231749.3:p.Gln164Ter
ENST00000360165.7:c.490C>T	ENSP00000353289.3:p.Gln164Ter
ENST00000442887.1:c.361C>T	ENSP00000393687.1:p.Gln121Ter
ENST00000443080.5:c.*263-121C>T	ENSP00000415661.1:n.*263-121C>T
ENST00000478269.5:n.475C>T
XM_005265216.2:c.253C>T	XP_005265273.1:p.Gln85Ter
XM_005265216.3:c.253C>T	XP_005265273.1:p.Gln85Ter