Canonical Allele Identifier: CA352942157

Gene: ZMYND10

Linked Data

• ClinVar Variation Id: 2009556
• ClinVar RCV Id: RCV002842480
• MyVariant Identifiers: chr3:g.50380586G>C (hg19) ; chr3:g.50343155G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343155G>C , CM000665.2:g.50343155G>C	GRCh38
NC_000003.11:g.50380586G>C , CM000665.1:g.50380586G>C	GRCh37
NC_000003.10:g.50355590G>C	NCBI36
NG_023270.1:g.2782C>G
NG_042828.1:g.7592C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.562C>G MANE Select	ENSP00000231749.3:p.Leu188Val
ENST00000231749.7:c.562C>G	ENSP00000231749.3:p.Leu188Val
ENST00000360165.7:c.562C>G	ENSP00000353289.3:p.Leu188Val
ENST00000442887.1:c.433C>G	ENSP00000393687.1:p.Leu145Val
ENST00000443080.5:c.*314C>G	ENSP00000415661.1:n.*314C>G
ENST00000475688.1:n.14C>G
NM_001308379.1:c.562C>G	NP_001295308.1:p.Leu188Val
NM_015896.2:c.562C>G	NP_056980.2:p.Leu188Val
NM_015896.3:c.562C>G	NP_056980.2:p.Leu188Val
XM_005265216.2:c.325C>G	XP_005265273.1:p.Leu109Val
XM_005265216.3:c.325C>G	XP_005265273.1:p.Leu109Val
NM_015896.4:c.562C>G MANE Select	NP_056980.2:p.Leu188Val
NM_001308379.2:c.562C>G	NP_001295308.1:p.Leu188Val