Canonical Allele Identifier: CA433711474

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50383044A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345613A>G , CM000665.2:g.50345613A>G	GRCh38
NC_000003.11:g.50383044A>G , CM000665.1:g.50383044A>G	GRCh37
NC_000003.10:g.50358048A>G	NCBI36
NG_023270.1:g.324T>C
NG_042828.1:g.5134T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-34T>C MANE Select	ENSP00000231749.3:n.-34T>C
ENST00000231749.7:c.-34T>C	ENSP00000231749.3:n.-34T>C
ENST00000360165.7:c.-34T>C	ENSP00000353289.3:n.-34T>C
ENST00000431869.1:c.-34T>C	ENSP00000391545.1:n.-34T>C
ENST00000442887.1:c.-116T>C	ENSP00000393687.1:n.-116T>C
ENST00000443080.5:c.-34T>C	ENSP00000415661.1:n.-34T>C
ENST00000468182.1:n.69T>C
NM_001308379.1:c.-34T>C	NP_001295308.1:n.-34T>C
NM_015896.2:c.-34T>C	NP_056980.2:n.-34T>C
NM_015896.3:c.-34T>C	NP_056980.2:n.-34T>C
XM_005265216.2:c.-162T>C	XP_005265273.1:n.-162T>C
XM_005265216.3:c.-162T>C	XP_005265273.1:n.-162T>C
NM_015896.4:c.-34T>C MANE Select	NP_056980.2:n.-34T>C
NM_001308379.2:c.-34T>C	NP_001295308.1:n.-34T>C