Canonical Allele Identifier: CA1363908854

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345621T= , CM000665.2:g.50345621T=	GRCh38
NC_000003.11:g.50383052T= , CM000665.1:g.50383052T=	GRCh37
NC_000003.10:g.50358056T=	NCBI36
NG_023270.1:g.316A=
NG_042828.1:g.5126A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-42A= MANE Select	ENSP00000231749.3:n.-42A=
ENST00000231749.7:c.-42A=	ENSP00000231749.3:n.-42A=
ENST00000360165.7:c.-42A=	ENSP00000353289.3:n.-42A=
ENST00000431869.1:c.-42A=	ENSP00000391545.1:n.-42A=
ENST00000442887.1:c.-124A=	ENSP00000393687.1:n.-124A=
ENST00000443080.5:c.-42A=	ENSP00000415661.1:n.-42A=
ENST00000468182.1:n.61A=
NM_001308379.1:c.-42A=	NP_001295308.1:n.-42A=
NM_015896.2:c.-42A=	NP_056980.2:n.-42A=
NM_015896.3:c.-42A=	NP_056980.2:n.-42A=
XM_005265216.2:c.-170A=	XP_005265273.1:n.-170A=
XM_005265216.3:c.-170A=	XP_005265273.1:n.-170A=
NM_015896.4:c.-42A= MANE Select	NP_056980.2:n.-42A=
NM_001308379.2:c.-42A=	NP_001295308.1:n.-42A=