Canonical Allele Identifier: CA433711724

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50345658-C-T
• MyVariant Identifiers: chr3:g.50383089C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345658C>T , CM000665.2:g.50345658C>T	GRCh38
NC_000003.11:g.50383089C>T , CM000665.1:g.50383089C>T	GRCh37
NC_000003.10:g.50358093C>T	NCBI36
NG_023270.1:g.279G>A
NG_042828.1:g.5089G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-79G>A MANE Select	ENSP00000231749.3:n.-79G>A
ENST00000231749.7:c.-79G>A	ENSP00000231749.3:n.-79G>A
ENST00000360165.7:c.-79G>A	ENSP00000353289.3:n.-79G>A
ENST00000431869.1:c.-79G>A	ENSP00000391545.1:n.-79G>A
ENST00000442887.1:c.-161G>A	ENSP00000393687.1:n.-161G>A
ENST00000443080.5:c.-79G>A	ENSP00000415661.1:n.-79G>A
ENST00000468182.1:n.24G>A
NM_001308379.1:c.-79G>A	NP_001295308.1:n.-79G>A
NM_015896.2:c.-79G>A	NP_056980.2:n.-79G>A
NM_015896.3:c.-79G>A	NP_056980.2:n.-79G>A
XM_005265216.2:c.-207G>A	XP_005265273.1:n.-207G>A
XM_005265216.3:c.-207G>A	XP_005265273.1:n.-207G>A
NM_015896.4:c.-79G>A MANE Select	NP_056980.2:n.-79G>A
NM_001308379.2:c.-79G>A	NP_001295308.1:n.-79G>A