Canonical Allele Identifier: CA542854451

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1279843700
• gnomAD v2: 3-50382677-T-TA
• gnomAD v4: 3-50345246-T-TA
• MyVariant Identifiers: chr3:g.50382677_50382678insA (hg19) ; chr3:g.50345246_50345247insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345248dup , CM000665.2:g.50345248dup	GRCh38
NC_000003.11:g.50382679dup , CM000665.1:g.50382679dup	GRCh37
NC_000003.10:g.50357683dup	NCBI36
NG_023270.1:g.690dup
NG_042828.1:g.5500dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.93-15dup MANE Select	ENSP00000231749.3:n.93-15dup
ENST00000231749.7:c.93-15dup	ENSP00000231749.3:n.93-15dup
ENST00000360165.7:c.93-15dup	ENSP00000353289.3:n.93-15dup
ENST00000431869.1:c.93-11dup	ENSP00000391545.1:n.93-11dup
ENST00000442887.1:c.-37-15dup	ENSP00000393687.1:n.-37-15dup
ENST00000443080.5:c.93-11dup	ENSP00000415661.1:n.93-11dup
ENST00000468182.1:n.195-15dup
NM_001308379.1:c.93-15dup	NP_001295308.1:n.93-15dup
NM_015896.2:c.93-15dup	NP_056980.2:n.93-15dup
NM_015896.3:c.93-15dup	NP_056980.2:n.93-15dup
XM_005265216.2:c.-37+241dup	XP_005265273.1:n.-37+241dup
XM_005265216.3:c.-37+241dup	XP_005265273.1:n.-37+241dup
NM_015896.4:c.93-15dup MANE Select	NP_056980.2:n.93-15dup
NM_001308379.2:c.93-15dup	NP_001295308.1:n.93-15dup