Canonical Allele Identifier: CA1363908895

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345726A= , CM000665.2:g.50345726A=	GRCh38
NC_000003.11:g.50383157A= , CM000665.1:g.50383157A=	GRCh37
NC_000003.10:g.50358161A=	NCBI36
NG_023270.1:g.211T=
NG_042828.1:g.5021T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-147T= MANE Select	ENSP00000231749.3:n.-147T=
ENST00000231749.7:c.-147T=	ENSP00000231749.3:n.-147T=
ENST00000360165.7:c.-147T=	ENSP00000353289.3:n.-147T=
NM_001308379.1:c.-147T=	NP_001295308.1:n.-147T=
NM_015896.3:c.-147T=	NP_056980.2:n.-147T=
XM_005265216.2:c.-275T=	XP_005265273.1:n.-275T=
NM_015896.4:c.-147T= MANE Select	NP_056980.2:n.-147T=
NM_001308379.2:c.-147T=	NP_001295308.1:n.-147T=