Canonical Allele Identifier: CA433711157

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50345538-C-T
• MyVariant Identifiers: chr3:g.50382969C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345538C>T , CM000665.2:g.50345538C>T	GRCh38
NC_000003.11:g.50382969C>T , CM000665.1:g.50382969C>T	GRCh37
NC_000003.10:g.50357973C>T	NCBI36
NG_023270.1:g.399G>A
NG_042828.1:g.5209G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.42G>A MANE Select	ENSP00000231749.3:p.Val14=
ENST00000231749.7:c.42G>A	ENSP00000231749.3:p.Val14=
ENST00000360165.7:c.42G>A	ENSP00000353289.3:p.Val14=
ENST00000431869.1:c.42G>A	ENSP00000391545.1:p.Val14=
ENST00000442887.1:c.-41G>A	ENSP00000393687.1:n.-41G>A
ENST00000443080.5:c.42G>A	ENSP00000415661.1:p.Val14=
ENST00000468182.1:n.144G>A
NM_001308379.1:c.42G>A	NP_001295308.1:p.Val14=
NM_015896.2:c.42G>A	NP_056980.2:p.Val14=
NM_015896.3:c.42G>A	NP_056980.2:p.Val14=
XM_005265216.2:c.-87G>A	XP_005265273.1:n.-87G>A
XM_005265216.3:c.-87G>A	XP_005265273.1:n.-87G>A
NM_015896.4:c.42G>A MANE Select	NP_056980.2:p.Val14=
NM_001308379.2:c.42G>A	NP_001295308.1:p.Val14=