Canonical Allele Identifier: CA1363903210

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343059G= , CM000665.2:g.50343059G=	GRCh38
NC_000003.11:g.50380490G= , CM000665.1:g.50380490G=	GRCh37
NC_000003.10:g.50355494G=	NCBI36
NG_023270.1:g.2878C=
NG_042828.1:g.7688C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.600-41C= MANE Select	ENSP00000231749.3:n.600-41C=
ENST00000231749.7:c.600-41C=	ENSP00000231749.3:n.600-41C=
ENST00000360165.7:c.599+59C=	ENSP00000353289.3:n.599+59C=
ENST00000442887.1:c.471-41C=	ENSP00000393687.1:n.471-41C=
ENST00000443080.5:c.*352-41C=	ENSP00000415661.1:n.*352-41C=
ENST00000475688.1:n.110C=
NM_001308379.1:c.599+59C=	NP_001295308.1:n.599+59C=
NM_015896.2:c.600-41C=	NP_056980.2:n.600-41C=
NM_015896.3:c.600-41C=	NP_056980.2:n.600-41C=
XM_005265216.2:c.363-41C=	XP_005265273.1:n.363-41C=
XM_005265216.3:c.363-41C=	XP_005265273.1:n.363-41C=
NM_015896.4:c.600-41C= MANE Select	NP_056980.2:n.600-41C=
NM_001308379.2:c.599+59C=	NP_001295308.1:n.599+59C=