Canonical Allele Identifier: CA352942131

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380579A>G (hg19) ; chr3:g.50343148A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343148A>G , CM000665.2:g.50343148A>G	GRCh38
NC_000003.11:g.50380579A>G , CM000665.1:g.50380579A>G	GRCh37
NC_000003.10:g.50355583A>G	NCBI36
NG_023270.1:g.2789T>C
NG_042828.1:g.7599T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.569T>C MANE Select	ENSP00000231749.3:p.Val190Ala
ENST00000231749.7:c.569T>C	ENSP00000231749.3:p.Val190Ala
ENST00000360165.7:c.569T>C	ENSP00000353289.3:p.Val190Ala
ENST00000442887.1:c.440T>C	ENSP00000393687.1:p.Val147Ala
ENST00000443080.5:c.*321T>C	ENSP00000415661.1:n.*321T>C
ENST00000475688.1:n.21T>C
NM_001308379.1:c.569T>C	NP_001295308.1:p.Val190Ala
NM_015896.2:c.569T>C	NP_056980.2:p.Val190Ala
NM_015896.3:c.569T>C	NP_056980.2:p.Val190Ala
XM_005265216.2:c.332T>C	XP_005265273.1:p.Val111Ala
XM_005265216.3:c.332T>C	XP_005265273.1:p.Val111Ala
NM_015896.4:c.569T>C MANE Select	NP_056980.2:p.Val190Ala
NM_001308379.2:c.569T>C	NP_001295308.1:p.Val190Ala