Canonical Allele Identifier: CA433709535

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1703442990
• COSMIC: COSM3916316 ; COSM3916317
• MyVariant Identifiers: chr3:g.50380626C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343195C>T , CM000665.2:g.50343195C>T	GRCh38
NC_000003.11:g.50380626C>T , CM000665.1:g.50380626C>T	GRCh37
NC_000003.10:g.50355630C>T	NCBI36
NG_023270.1:g.2742G>A
NG_042828.1:g.7552G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.522G>A MANE Select	ENSP00000231749.3:p.Lys174=
ENST00000231749.7:c.522G>A	ENSP00000231749.3:p.Lys174=
ENST00000360165.7:c.522G>A	ENSP00000353289.3:p.Lys174=
ENST00000442887.1:c.393G>A	ENSP00000393687.1:p.Lys131=
ENST00000443080.5:c.*274G>A	ENSP00000415661.1:n.*274G>A
ENST00000478269.5:n.607G>A
NM_001308379.1:c.522G>A	NP_001295308.1:p.Lys174=
NM_015896.2:c.522G>A	NP_056980.2:p.Lys174=
NM_015896.3:c.522G>A	NP_056980.2:p.Lys174=
XM_005265216.2:c.285G>A	XP_005265273.1:p.Lys95=
XM_005265216.3:c.285G>A	XP_005265273.1:p.Lys95=
NM_015896.4:c.522G>A MANE Select	NP_056980.2:p.Lys174=
NM_001308379.2:c.522G>A	NP_001295308.1:p.Lys174=