Canonical Allele Identifier: CA433710415

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382630C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345199C>G , CM000665.2:g.50345199C>G	GRCh38
NC_000003.11:g.50382630C>G , CM000665.1:g.50382630C>G	GRCh37
NC_000003.10:g.50357634C>G	NCBI36
NG_023270.1:g.738G>C
NG_042828.1:g.5548G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.126G>C MANE Select	ENSP00000231749.3:p.Leu42=
ENST00000231749.7:c.126G>C	ENSP00000231749.3:p.Leu42=
ENST00000360165.7:c.126G>C	ENSP00000353289.3:p.Leu42=
ENST00000431869.1:c.*16G>C	ENSP00000391545.1:n.*16G>C
ENST00000442887.1:c.-4G>C	ENSP00000393687.1:n.-4G>C
ENST00000443080.5:c.*16G>C	ENSP00000415661.1:n.*16G>C
ENST00000468182.1:n.228G>C
NM_001308379.1:c.126G>C	NP_001295308.1:p.Leu42=
NM_015896.2:c.126G>C	NP_056980.2:p.Leu42=
NM_015896.3:c.126G>C	NP_056980.2:p.Leu42=
XM_005265216.2:c.-37+289G>C	XP_005265273.1:n.-37+289G>C
XM_005265216.3:c.-37+289G>C	XP_005265273.1:n.-37+289G>C
NM_015896.4:c.126G>C MANE Select	NP_056980.2:p.Leu42=
NM_001308379.2:c.126G>C	NP_001295308.1:p.Leu42=