Canonical Allele Identifier: CA2577791043

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343093G>A , CM000665.2:g.50343093G>A	GRCh38
NC_000003.11:g.50380524G>A , CM000665.1:g.50380524G>A	GRCh37
NC_000003.10:g.50355528G>A	NCBI36
NG_023270.1:g.2844C>T
NG_042828.1:g.7654C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.599+25C>T MANE Select	ENSP00000231749.3:n.599+25C>T
ENST00000231749.7:c.599+25C>T	ENSP00000231749.3:n.599+25C>T
ENST00000360165.7:c.599+25C>T	ENSP00000353289.3:n.599+25C>T
ENST00000442887.1:c.470+25C>T	ENSP00000393687.1:n.470+25C>T
ENST00000443080.5:c.*351+25C>T	ENSP00000415661.1:n.*351+25C>T
ENST00000475688.1:n.76C>T
NM_001308379.1:c.599+25C>T	NP_001295308.1:n.599+25C>T
NM_015896.2:c.599+25C>T	NP_056980.2:n.599+25C>T
NM_015896.3:c.599+25C>T	NP_056980.2:n.599+25C>T
XM_005265216.2:c.362+25C>T	XP_005265273.1:n.362+25C>T
XM_005265216.3:c.362+25C>T	XP_005265273.1:n.362+25C>T
NM_015896.4:c.599+25C>T MANE Select	NP_056980.2:n.599+25C>T
NM_001308379.2:c.599+25C>T	NP_001295308.1:n.599+25C>T