Canonical Allele Identifier: CA433710402

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382627G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345196G>A , CM000665.2:g.50345196G>A	GRCh38
NC_000003.11:g.50382627G>A , CM000665.1:g.50382627G>A	GRCh37
NC_000003.10:g.50357631G>A	NCBI36
NG_023270.1:g.741C>T
NG_042828.1:g.5551C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.129C>T MANE Select	ENSP00000231749.3:p.Asn43=
ENST00000231749.7:c.129C>T	ENSP00000231749.3:p.Asn43=
ENST00000360165.7:c.129C>T	ENSP00000353289.3:p.Asn43=
ENST00000431869.1:c.*19C>T	ENSP00000391545.1:n.*19C>T
ENST00000442887.1:c.-1C>T	ENSP00000393687.1:n.-1C>T
ENST00000443080.5:c.*19C>T	ENSP00000415661.1:n.*19C>T
ENST00000468182.1:n.231C>T
NM_001308379.1:c.129C>T	NP_001295308.1:p.Asn43=
NM_015896.2:c.129C>T	NP_056980.2:p.Asn43=
NM_015896.3:c.129C>T	NP_056980.2:p.Asn43=
XM_005265216.2:c.-37+292C>T	XP_005265273.1:n.-37+292C>T
XM_005265216.3:c.-37+292C>T	XP_005265273.1:n.-37+292C>T
NM_015896.4:c.129C>T MANE Select	NP_056980.2:p.Asn43=
NM_001308379.2:c.129C>T	NP_001295308.1:p.Asn43=