Canonical Allele Identifier: CA352942106

Gene: ZMYND10

Linked Data

• ClinVar Variation Id: 2097320
• ClinVar RCV Id: RCV003028436
• gnomAD v4: 3-50343139-T-C
• MyVariant Identifiers: chr3:g.50380570T>C (hg19) ; chr3:g.50343139T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343139T>C , CM000665.2:g.50343139T>C	GRCh38
NC_000003.11:g.50380570T>C , CM000665.1:g.50380570T>C	GRCh37
NC_000003.10:g.50355574T>C	NCBI36
NG_023270.1:g.2798A>G
NG_042828.1:g.7608A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.578A>G MANE Select	ENSP00000231749.3:p.Tyr193Cys
ENST00000231749.7:c.578A>G	ENSP00000231749.3:p.Tyr193Cys
ENST00000360165.7:c.578A>G	ENSP00000353289.3:p.Tyr193Cys
ENST00000442887.1:c.449A>G	ENSP00000393687.1:p.Tyr150Cys
ENST00000443080.5:c.*330A>G	ENSP00000415661.1:n.*330A>G
ENST00000475688.1:n.30A>G
NM_001308379.1:c.578A>G	NP_001295308.1:p.Tyr193Cys
NM_015896.2:c.578A>G	NP_056980.2:p.Tyr193Cys
NM_015896.3:c.578A>G	NP_056980.2:p.Tyr193Cys
XM_005265216.2:c.341A>G	XP_005265273.1:p.Tyr114Cys
XM_005265216.3:c.341A>G	XP_005265273.1:p.Tyr114Cys
NM_015896.4:c.578A>G MANE Select	NP_056980.2:p.Tyr193Cys
NM_001308379.2:c.578A>G	NP_001295308.1:p.Tyr193Cys