Canonical Allele Identifier: CA1363908889

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345718C= , CM000665.2:g.50345718C=	GRCh38
NC_000003.11:g.50383149C= , CM000665.1:g.50383149C=	GRCh37
NC_000003.10:g.50358153C=	NCBI36
NG_023270.1:g.219G=
NG_042828.1:g.5029G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-139G= MANE Select	ENSP00000231749.3:n.-139G=
ENST00000231749.7:c.-139G=	ENSP00000231749.3:n.-139G=
ENST00000360165.7:c.-139G=	ENSP00000353289.3:n.-139G=
ENST00000431869.1:c.-139G=	ENSP00000391545.1:n.-139G=
ENST00000442887.1:c.-221G=	ENSP00000393687.1:n.-221G=
NM_001308379.1:c.-139G=	NP_001295308.1:n.-139G=
NM_015896.2:c.-139G=	NP_056980.2:n.-139G=
NM_015896.3:c.-139G=	NP_056980.2:n.-139G=
XM_005265216.2:c.-267G=	XP_005265273.1:n.-267G=
NM_015896.4:c.-139G= MANE Select	NP_056980.2:n.-139G=
NM_001308379.2:c.-139G=	NP_001295308.1:n.-139G=