Canonical Allele Identifier: CA2417091

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342546T>C , CM000665.2:g.50342546T>C	GRCh38
NC_000003.11:g.50379977T>C , CM000665.1:g.50379977T>C	GRCh37
NC_000003.10:g.50354981T>C	NCBI36
NG_023270.1:g.3391A>G
NG_042828.1:g.8201A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015896.4:c.724A>G MANE Select	NP_056980.2:p.Ser242Gly
ENST00000231749.8:c.724A>G MANE Select	ENSP00000231749.3:p.Ser242Gly
NM_001308379.1:c.709A>G	NP_001295308.1:p.Ser237Gly
NM_001308379.2:c.709A>G	NP_001295308.1:p.Ser237Gly
NM_015896.2:c.724A>G	NP_056980.2:p.Ser242Gly
NM_015896.3:c.724A>G	NP_056980.2:p.Ser242Gly
ENST00000231749.7:c.724A>G	ENSP00000231749.3:p.Ser242Gly
ENST00000360165.7:c.709A>G	ENSP00000353289.3:p.Ser237Gly
ENST00000442887.1:c.595A>G	ENSP00000393687.1:p.Ser199Gly
ENST00000443080.5:c.*476A>G	ENSP00000415661.1:n.*476A>G
ENST00000475688.1:n.623A>G
XM_005265216.2:c.487A>G	XP_005265273.1:p.Ser163Gly
XM_005265216.3:c.487A>G	XP_005265273.1:p.Ser163Gly