Canonical Allele Identifier: CA352946099

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382972T>G (hg19) ; chr3:g.50345541T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345541T>G , CM000665.2:g.50345541T>G	GRCh38
NC_000003.11:g.50382972T>G , CM000665.1:g.50382972T>G	GRCh37
NC_000003.10:g.50357976T>G	NCBI36
NG_023270.1:g.396A>C
NG_042828.1:g.5206A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000231749.8:c.39A>C MANE Select	ENSP00000231749.3:p.Glu13Asp
ENST00000231749.7:c.39A>C	ENSP00000231749.3:p.Glu13Asp
ENST00000360165.7:c.39A>C	ENSP00000353289.3:p.Glu13Asp
ENST00000431869.1:c.39A>C	ENSP00000391545.1:p.Glu13Asp
ENST00000442887.1:c.-44A>C	ENSP00000393687.1:n.-44A>C
ENST00000443080.5:c.39A>C	ENSP00000415661.1:p.Glu13Asp
ENST00000468182.1:n.141A>C
NM_001308379.1:c.39A>C	NP_001295308.1:p.Glu13Asp
NM_015896.2:c.39A>C	NP_056980.2:p.Glu13Asp
NM_015896.3:c.39A>C	NP_056980.2:p.Glu13Asp
XM_005265216.2:c.-90A>C	XP_005265273.1:n.-90A>C
XM_005265216.3:c.-90A>C	XP_005265273.1:n.-90A>C
NM_015896.4:c.39A>C MANE Select	NP_056980.2:p.Glu13Asp
NM_001308379.2:c.39A>C	NP_001295308.1:p.Glu13Asp