Canonical Allele Identifier: CA433709064

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380385G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342954G>A , CM000665.2:g.50342954G>A	GRCh38
NC_000003.11:g.50380385G>A , CM000665.1:g.50380385G>A	GRCh37
NC_000003.10:g.50355389G>A	NCBI36
NG_023270.1:g.2983C>T
NG_042828.1:g.7793C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.664C>T MANE Select	ENSP00000231749.3:p.Leu222=
ENST00000231749.7:c.664C>T	ENSP00000231749.3:p.Leu222=
ENST00000360165.7:c.599+164C>T	ENSP00000353289.3:n.599+164C>T
ENST00000442887.1:c.535C>T	ENSP00000393687.1:p.Leu179=
ENST00000443080.5:c.*416C>T	ENSP00000415661.1:n.*416C>T
ENST00000475688.1:n.215C>T
NM_001308379.1:c.599+164C>T	NP_001295308.1:n.599+164C>T
NM_015896.2:c.664C>T	NP_056980.2:p.Leu222=
NM_015896.3:c.664C>T	NP_056980.2:p.Leu222=
XM_005265216.2:c.427C>T	XP_005265273.1:p.Leu143=
XM_005265216.3:c.427C>T	XP_005265273.1:p.Leu143=
NM_015896.4:c.664C>T MANE Select	NP_056980.2:p.Leu222=
NM_001308379.2:c.599+164C>T	NP_001295308.1:n.599+164C>T