Canonical Allele Identifier: CA433711883

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50383122A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345691A>G , CM000665.2:g.50345691A>G	GRCh38
NC_000003.11:g.50383122A>G , CM000665.1:g.50383122A>G	GRCh37
NC_000003.10:g.50358126A>G	NCBI36
NG_023270.1:g.246T>C
NG_042828.1:g.5056T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-112T>C MANE Select	ENSP00000231749.3:n.-112T>C
ENST00000231749.7:c.-112T>C	ENSP00000231749.3:n.-112T>C
ENST00000360165.7:c.-112T>C	ENSP00000353289.3:n.-112T>C
ENST00000431869.1:c.-112T>C	ENSP00000391545.1:n.-112T>C
ENST00000442887.1:c.-194T>C	ENSP00000393687.1:n.-194T>C
NM_001308379.1:c.-112T>C	NP_001295308.1:n.-112T>C
NM_015896.2:c.-112T>C	NP_056980.2:n.-112T>C
NM_015896.3:c.-112T>C	NP_056980.2:n.-112T>C
XM_005265216.2:c.-240T>C	XP_005265273.1:n.-240T>C
XM_005265216.3:c.-240T>C	XP_005265273.1:n.-240T>C
NM_015896.4:c.-112T>C MANE Select	NP_056980.2:n.-112T>C
NM_001308379.2:c.-112T>C	NP_001295308.1:n.-112T>C