Canonical Allele Identifier: CA1363903187

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1575554638

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343034T>G , CM000665.2:g.50343034T>G	GRCh38
NC_000003.11:g.50380465T>G , CM000665.1:g.50380465T>G	GRCh37
NC_000003.10:g.50355469T>G	NCBI36
NG_023270.1:g.2903A>C
NG_042828.1:g.7713A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.600-16A>C MANE Select	ENSP00000231749.3:n.600-16A>C
ENST00000231749.7:c.600-16A>C	ENSP00000231749.3:n.600-16A>C
ENST00000360165.7:c.599+84A>C	ENSP00000353289.3:n.599+84A>C
ENST00000442887.1:c.471-16A>C	ENSP00000393687.1:n.471-16A>C
ENST00000443080.5:c.*352-16A>C	ENSP00000415661.1:n.*352-16A>C
ENST00000475688.1:n.135A>C
NM_001308379.1:c.599+84A>C	NP_001295308.1:n.599+84A>C
NM_015896.2:c.600-16A>C	NP_056980.2:n.600-16A>C
NM_015896.3:c.600-16A>C	NP_056980.2:n.600-16A>C
XM_005265216.2:c.363-16A>C	XP_005265273.1:n.363-16A>C
XM_005265216.3:c.363-16A>C	XP_005265273.1:n.363-16A>C
NM_015896.4:c.600-16A>C MANE Select	NP_056980.2:n.600-16A>C
NM_001308379.2:c.599+84A>C	NP_001295308.1:n.599+84A>C