Canonical Allele Identifier: CA352942054

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380555A>G (hg19) ; chr3:g.50343124A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343124A>G , CM000665.2:g.50343124A>G	GRCh38
NC_000003.11:g.50380555A>G , CM000665.1:g.50380555A>G	GRCh37
NC_000003.10:g.50355559A>G	NCBI36
NG_023270.1:g.2813T>C
NG_042828.1:g.7623T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.593T>C MANE Select	ENSP00000231749.3:p.Val198Ala
ENST00000231749.7:c.593T>C	ENSP00000231749.3:p.Val198Ala
ENST00000360165.7:c.593T>C	ENSP00000353289.3:p.Val198Ala
ENST00000442887.1:c.464T>C	ENSP00000393687.1:p.Val155Ala
ENST00000443080.5:c.*345T>C	ENSP00000415661.1:n.*345T>C
ENST00000475688.1:n.45T>C
NM_001308379.1:c.593T>C	NP_001295308.1:p.Val198Ala
NM_015896.2:c.593T>C	NP_056980.2:p.Val198Ala
NM_015896.3:c.593T>C	NP_056980.2:p.Val198Ala
XM_005265216.2:c.356T>C	XP_005265273.1:p.Val119Ala
XM_005265216.3:c.356T>C	XP_005265273.1:p.Val119Ala
NM_015896.4:c.593T>C MANE Select	NP_056980.2:p.Val198Ala
NM_001308379.2:c.593T>C	NP_001295308.1:p.Val198Ala