Canonical Allele Identifier: CA352942269

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380617C>G (hg19) ; chr3:g.50343186C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343186C>G , CM000665.2:g.50343186C>G	GRCh38
NC_000003.11:g.50380617C>G , CM000665.1:g.50380617C>G	GRCh37
NC_000003.10:g.50355621C>G	NCBI36
NG_023270.1:g.2751G>C
NG_042828.1:g.7561G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.531G>C MANE Select	ENSP00000231749.3:p.Glu177Asp
ENST00000231749.7:c.531G>C	ENSP00000231749.3:p.Glu177Asp
ENST00000360165.7:c.531G>C	ENSP00000353289.3:p.Glu177Asp
ENST00000442887.1:c.402G>C	ENSP00000393687.1:p.Glu134Asp
ENST00000443080.5:c.*283G>C	ENSP00000415661.1:n.*283G>C
ENST00000478269.5:n.616G>C
NM_001308379.1:c.531G>C	NP_001295308.1:p.Glu177Asp
NM_015896.2:c.531G>C	NP_056980.2:p.Glu177Asp
NM_015896.3:c.531G>C	NP_056980.2:p.Glu177Asp
XM_005265216.2:c.294G>C	XP_005265273.1:p.Glu98Asp
XM_005265216.3:c.294G>C	XP_005265273.1:p.Glu98Asp
NM_015896.4:c.531G>C MANE Select	NP_056980.2:p.Glu177Asp
NM_001308379.2:c.531G>C	NP_001295308.1:p.Glu177Asp