Canonical Allele Identifier: CA433710291

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382594C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345163C>T , CM000665.2:g.50345163C>T	GRCh38
NC_000003.11:g.50382594C>T , CM000665.1:g.50382594C>T	GRCh37
NC_000003.10:g.50357598C>T	NCBI36
NG_023270.1:g.774G>A
NG_042828.1:g.5584G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.162G>A MANE Select	ENSP00000231749.3:p.Gln54=
ENST00000231749.7:c.162G>A	ENSP00000231749.3:p.Gln54=
ENST00000360165.7:c.162G>A	ENSP00000353289.3:p.Gln54=
ENST00000431869.1:c.*52G>A	ENSP00000391545.1:n.*52G>A
ENST00000442887.1:c.33G>A	ENSP00000393687.1:p.Gln11=
ENST00000443080.5:c.*52G>A	ENSP00000415661.1:n.*52G>A
ENST00000468182.1:n.264G>A
NM_001308379.1:c.162G>A	NP_001295308.1:p.Gln54=
NM_015896.2:c.162G>A	NP_056980.2:p.Gln54=
NM_015896.3:c.162G>A	NP_056980.2:p.Gln54=
XM_005265216.2:c.-37+325G>A	XP_005265273.1:n.-37+325G>A
XM_005265216.3:c.-37+325G>A	XP_005265273.1:n.-37+325G>A
NM_015896.4:c.162G>A MANE Select	NP_056980.2:p.Gln54=
NM_001308379.2:c.162G>A	NP_001295308.1:p.Gln54=