Canonical Allele Identifier: CA433709493

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380614C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343183C>G , CM000665.2:g.50343183C>G	GRCh38
NC_000003.11:g.50380614C>G , CM000665.1:g.50380614C>G	GRCh37
NC_000003.10:g.50355618C>G	NCBI36
NG_023270.1:g.2754G>C
NG_042828.1:g.7564G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.534G>C MANE Select	ENSP00000231749.3:p.Leu178=
ENST00000231749.7:c.534G>C	ENSP00000231749.3:p.Leu178=
ENST00000360165.7:c.534G>C	ENSP00000353289.3:p.Leu178=
ENST00000442887.1:c.405G>C	ENSP00000393687.1:p.Leu135=
ENST00000443080.5:c.*286G>C	ENSP00000415661.1:n.*286G>C
ENST00000478269.5:n.619G>C
NM_001308379.1:c.534G>C	NP_001295308.1:p.Leu178=
NM_015896.2:c.534G>C	NP_056980.2:p.Leu178=
NM_015896.3:c.534G>C	NP_056980.2:p.Leu178=
XM_005265216.2:c.297G>C	XP_005265273.1:p.Leu99=
XM_005265216.3:c.297G>C	XP_005265273.1:p.Leu99=
NM_015896.4:c.534G>C MANE Select	NP_056980.2:p.Leu178=
NM_001308379.2:c.534G>C	NP_001295308.1:p.Leu178=