Canonical Allele Identifier: CA352945633

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382614G>T (hg19) ; chr3:g.50345183G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345183G>T , CM000665.2:g.50345183G>T	GRCh38
NC_000003.11:g.50382614G>T , CM000665.1:g.50382614G>T	GRCh37
NC_000003.10:g.50357618G>T	NCBI36
NG_023270.1:g.754C>A
NG_042828.1:g.5564C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.142C>A MANE Select	ENSP00000231749.3:p.Leu48Ile
ENST00000231749.7:c.142C>A	ENSP00000231749.3:p.Leu48Ile
ENST00000360165.7:c.142C>A	ENSP00000353289.3:p.Leu48Ile
ENST00000431869.1:c.*32C>A	ENSP00000391545.1:n.*32C>A
ENST00000442887.1:c.13C>A	ENSP00000393687.1:p.Leu5Ile
ENST00000443080.5:c.*32C>A	ENSP00000415661.1:n.*32C>A
ENST00000468182.1:n.244C>A
NM_001308379.1:c.142C>A	NP_001295308.1:p.Leu48Ile
NM_015896.2:c.142C>A	NP_056980.2:p.Leu48Ile
NM_015896.3:c.142C>A	NP_056980.2:p.Leu48Ile
XM_005265216.2:c.-37+305C>A	XP_005265273.1:n.-37+305C>A
XM_005265216.3:c.-37+305C>A	XP_005265273.1:n.-37+305C>A
NM_015896.4:c.142C>A MANE Select	NP_056980.2:p.Leu48Ile
NM_001308379.2:c.142C>A	NP_001295308.1:p.Leu48Ile