Canonical Allele Identifier: CA2417000

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50341835G>A , CM000665.2:g.50341835G>A	GRCh38
NC_000003.11:g.50379266G>A , CM000665.1:g.50379266G>A	GRCh37
NC_000003.10:g.50354270G>A	NCBI36
NG_023270.1:g.4102C>T
NG_042828.1:g.8912C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015896.4:c.1096C>T MANE Select	NP_056980.2:p.Gln366Ter
ENST00000231749.8:c.1096C>T MANE Select	ENSP00000231749.3:p.Gln366Ter
NM_001308379.1:c.1081C>T	NP_001295308.1:p.Gln361Ter
NM_001308379.2:c.1081C>T	NP_001295308.1:p.Gln361Ter
NM_015896.2:c.1096C>T	NP_056980.2:p.Gln366Ter
NM_015896.3:c.1096C>T	NP_056980.2:p.Gln366Ter
ENST00000231749.7:c.1096C>T	ENSP00000231749.3:p.Gln366Ter
ENST00000360165.7:c.1081C>T	ENSP00000353289.3:p.Gln361Ter
ENST00000475688.1:n.1251C>T
ENST00000490675.5:n.149C>T
XM_005265216.2:c.859C>T	XP_005265273.1:p.Gln287Ter
XM_005265216.3:c.859C>T	XP_005265273.1:p.Gln287Ter