Canonical Allele Identifier: CA352941676

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380373T>G (hg19) ; chr3:g.50342942T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342942T>G , CM000665.2:g.50342942T>G	GRCh38
NC_000003.11:g.50380373T>G , CM000665.1:g.50380373T>G	GRCh37
NC_000003.10:g.50355377T>G	NCBI36
NG_023270.1:g.2995A>C
NG_042828.1:g.7805A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.676A>C MANE Select	ENSP00000231749.3:p.Ser226Arg
ENST00000231749.7:c.676A>C	ENSP00000231749.3:p.Ser226Arg
ENST00000360165.7:c.599+176A>C	ENSP00000353289.3:n.599+176A>C
ENST00000442887.1:c.547A>C	ENSP00000393687.1:p.Ser183Arg
ENST00000443080.5:c.*428A>C	ENSP00000415661.1:n.*428A>C
ENST00000475688.1:n.227A>C
NM_001308379.1:c.599+176A>C	NP_001295308.1:n.599+176A>C
NM_015896.2:c.676A>C	NP_056980.2:p.Ser226Arg
NM_015896.3:c.676A>C	NP_056980.2:p.Ser226Arg
XM_005265216.2:c.439A>C	XP_005265273.1:p.Ser147Arg
XM_005265216.3:c.439A>C	XP_005265273.1:p.Ser147Arg
NM_015896.4:c.676A>C MANE Select	NP_056980.2:p.Ser226Arg
NM_001308379.2:c.599+176A>C	NP_001295308.1:n.599+176A>C