Canonical Allele Identifier: CA1363908892

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345723G= , CM000665.2:g.50345723G=	GRCh38
NC_000003.11:g.50383154G= , CM000665.1:g.50383154G=	GRCh37
NC_000003.10:g.50358158G=	NCBI36
NG_023270.1:g.214C=
NG_042828.1:g.5024C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-144C= MANE Select	ENSP00000231749.3:n.-144C=
ENST00000231749.7:c.-144C=	ENSP00000231749.3:n.-144C=
ENST00000360165.7:c.-144C=	ENSP00000353289.3:n.-144C=
NM_001308379.1:c.-144C=	NP_001295308.1:n.-144C=
NM_015896.2:c.-144C=	NP_056980.2:n.-144C=
NM_015896.3:c.-144C=	NP_056980.2:n.-144C=
XM_005265216.2:c.-272C=	XP_005265273.1:n.-272C=
NM_015896.4:c.-144C= MANE Select	NP_056980.2:n.-144C=
NM_001308379.2:c.-144C=	NP_001295308.1:n.-144C=