Canonical Allele Identifier: CA352941845

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50342977-T-A
• MyVariant Identifiers: chr3:g.50380408T>A (hg19) ; chr3:g.50342977T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342977T>A , CM000665.2:g.50342977T>A	GRCh38
NC_000003.11:g.50380408T>A , CM000665.1:g.50380408T>A	GRCh37
NC_000003.10:g.50355412T>A	NCBI36
NG_023270.1:g.2960A>T
NG_042828.1:g.7770A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.641A>T MANE Select	ENSP00000231749.3:p.Asn214Ile
ENST00000231749.7:c.641A>T	ENSP00000231749.3:p.Asn214Ile
ENST00000360165.7:c.599+141A>T	ENSP00000353289.3:n.599+141A>T
ENST00000442887.1:c.512A>T	ENSP00000393687.1:p.Asn171Ile
ENST00000443080.5:c.*393A>T	ENSP00000415661.1:n.*393A>T
ENST00000475688.1:n.192A>T
NM_001308379.1:c.599+141A>T	NP_001295308.1:n.599+141A>T
NM_015896.2:c.641A>T	NP_056980.2:p.Asn214Ile
NM_015896.3:c.641A>T	NP_056980.2:p.Asn214Ile
XM_005265216.2:c.404A>T	XP_005265273.1:p.Asn135Ile
XM_005265216.3:c.404A>T	XP_005265273.1:p.Asn135Ile
NM_015896.4:c.641A>T MANE Select	NP_056980.2:p.Asn214Ile
NM_001308379.2:c.599+141A>T	NP_001295308.1:n.599+141A>T