Canonical Allele Identifier: CA352946119

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382977C>T (hg19) ; chr3:g.50345546C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345546C>T , CM000665.2:g.50345546C>T	GRCh38
NC_000003.11:g.50382977C>T , CM000665.1:g.50382977C>T	GRCh37
NC_000003.10:g.50357981C>T	NCBI36
NG_023270.1:g.391G>A
NG_042828.1:g.5201G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000231749.8:c.34G>A MANE Select	ENSP00000231749.3:p.Ala12Thr
ENST00000231749.7:c.34G>A	ENSP00000231749.3:p.Ala12Thr
ENST00000360165.7:c.34G>A	ENSP00000353289.3:p.Ala12Thr
ENST00000431869.1:c.34G>A	ENSP00000391545.1:p.Ala12Thr
ENST00000442887.1:c.-49G>A	ENSP00000393687.1:n.-49G>A
ENST00000443080.5:c.34G>A	ENSP00000415661.1:p.Ala12Thr
ENST00000468182.1:n.136G>A
NM_001308379.1:c.34G>A	NP_001295308.1:p.Ala12Thr
NM_015896.2:c.34G>A	NP_056980.2:p.Ala12Thr
NM_015896.3:c.34G>A	NP_056980.2:p.Ala12Thr
XM_005265216.2:c.-95G>A	XP_005265273.1:n.-95G>A
XM_005265216.3:c.-95G>A	XP_005265273.1:n.-95G>A
NM_015896.4:c.34G>A MANE Select	NP_056980.2:p.Ala12Thr
NM_001308379.2:c.34G>A	NP_001295308.1:p.Ala12Thr