Canonical Allele Identifier: CA352942066

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50343128-A-G
• MyVariant Identifiers: chr3:g.50380559A>G (hg19) ; chr3:g.50343128A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343128A>G , CM000665.2:g.50343128A>G	GRCh38
NC_000003.11:g.50380559A>G , CM000665.1:g.50380559A>G	GRCh37
NC_000003.10:g.50355563A>G	NCBI36
NG_023270.1:g.2809T>C
NG_042828.1:g.7619T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.589T>C MANE Select	ENSP00000231749.3:p.Cys197Arg
ENST00000231749.7:c.589T>C	ENSP00000231749.3:p.Cys197Arg
ENST00000360165.7:c.589T>C	ENSP00000353289.3:p.Cys197Arg
ENST00000442887.1:c.460T>C	ENSP00000393687.1:p.Cys154Arg
ENST00000443080.5:c.*341T>C	ENSP00000415661.1:n.*341T>C
ENST00000475688.1:n.41T>C
NM_001308379.1:c.589T>C	NP_001295308.1:p.Cys197Arg
NM_015896.2:c.589T>C	NP_056980.2:p.Cys197Arg
NM_015896.3:c.589T>C	NP_056980.2:p.Cys197Arg
XM_005265216.2:c.352T>C	XP_005265273.1:p.Cys118Arg
XM_005265216.3:c.352T>C	XP_005265273.1:p.Cys118Arg
NM_015896.4:c.589T>C MANE Select	NP_056980.2:p.Cys197Arg
NM_001308379.2:c.589T>C	NP_001295308.1:p.Cys197Arg