Canonical Allele Identifier: CA352942097

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380568T>A (hg19) ; chr3:g.50343137T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343137T>A , CM000665.2:g.50343137T>A	GRCh38
NC_000003.11:g.50380568T>A , CM000665.1:g.50380568T>A	GRCh37
NC_000003.10:g.50355572T>A	NCBI36
NG_023270.1:g.2800A>T
NG_042828.1:g.7610A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.580A>T MANE Select	ENSP00000231749.3:p.Ile194Phe
ENST00000231749.7:c.580A>T	ENSP00000231749.3:p.Ile194Phe
ENST00000360165.7:c.580A>T	ENSP00000353289.3:p.Ile194Phe
ENST00000442887.1:c.451A>T	ENSP00000393687.1:p.Ile151Phe
ENST00000443080.5:c.*332A>T	ENSP00000415661.1:n.*332A>T
ENST00000475688.1:n.32A>T
NM_001308379.1:c.580A>T	NP_001295308.1:p.Ile194Phe
NM_015896.2:c.580A>T	NP_056980.2:p.Ile194Phe
NM_015896.3:c.580A>T	NP_056980.2:p.Ile194Phe
XM_005265216.2:c.343A>T	XP_005265273.1:p.Ile115Phe
XM_005265216.3:c.343A>T	XP_005265273.1:p.Ile115Phe
NM_015896.4:c.580A>T MANE Select	NP_056980.2:p.Ile194Phe
NM_001308379.2:c.580A>T	NP_001295308.1:p.Ile194Phe